diff --git a/README.md b/README.md
index 7964db4cf..274df6e7a 100644
--- a/README.md
+++ b/README.md
@@ -71,6 +71,21 @@ Katsu Metadata Service is a service to store epigenomic metadata.
 6. Rest api service handles all generic functionality shared among other services
 
 
+## Schemas
+### Clinical Data
+
+Katsu implements the [Phenopacket V1.0.0](https://phenopacket-schema.readthedocs.io/en/1.0.0/) schema for clinical data.
+
+The schema definition for the phenopacket object is located in [chord_metadata_service/phenopackets/schemas.py](https://github.com/bento-platform/katsu/blob/4ab3c55d6052994ef69b188fb872261c47de24e0/chord_metadata_service/phenopackets/schemas.py#L336).
+
+### Experiments
+
+Katsu's experiments schemas are based on the IHEC [schema](https://github.com/IHEC/ihec-ecosystems/blob/master/docs/metadata/2.0/Ihec_metadata_specification.md#experiments), which is based on EBI/SRA schemas.
+
+The value options for `library_strategy` and `library_selection` are read from [chord_metadata_service/ontologies/xsd/SRA.experiment.xsd.xml](./chord_metadata_service/ontologies/xsd/SRA.experiment.xsd.xml), downloaded from the EBI's [SRA v1.5 database](http://ftp.ebi.ac.uk/pub/databases/ena/doc/xsd/sra_1_5/).
+
+The `SRA.experiment.xsd.xml` file is licensed under Apache License V2.0, the full copyright text is included in the file's header.
+
 ## REST API highlights
 
 * Swagger schema docs can be found 
diff --git a/chord_metadata_service/chord/ingest/exceptions.py b/chord_metadata_service/chord/ingest/exceptions.py
index bea8da514..7f362a715 100644
--- a/chord_metadata_service/chord/ingest/exceptions.py
+++ b/chord_metadata_service/chord/ingest/exceptions.py
@@ -1,7 +1,113 @@
+from typing import List, Optional
+from jsonschema.exceptions import ValidationError
+from chord_metadata_service import __version__
+from chord_metadata_service.experiments.schemas import EXPERIMENT_SCHEMA_CHANGES
+from chord_metadata_service.chord.data_types import DATA_TYPE_EXPERIMENT, DATA_TYPE_PHENOPACKET
+
 __all__ = [
     "IngestError",
 ]
 
 
+DATA_TYPE_SCHEMA_CHANGES = {
+    DATA_TYPE_EXPERIMENT: EXPERIMENT_SCHEMA_CHANGES,
+    DATA_TYPE_PHENOPACKET: None
+}
+
+
+def parse_validation_errors(errors: List[ValidationError]) -> Optional[List[dict]]:
+    """
+    Accepts a list of jsonschema ValidationError and converts them to a client error format.
+
+    Parameters:
+        errors (List[ValidationError]): errors raised by jsonschema during validation
+    Returns:
+        List[dict]:
+            dict:
+                schema_path (str): Schema path string (e.g "properties.library_strategy")
+                faulty_value (str | obj): The value at the schema_path causing the error
+                property_schema (dict): JSON schema of the property (includes valid options)
+                message (str): The ValidationError.message
+    """
+    error_descriptions = []
+    for error in errors:
+        schema_path = ".".join(error.schema_path)
+        error_descriptions.append({
+            "schema_path": schema_path,
+            "faulty_value": error.instance,
+            "message": error.message,
+            "property_schema": error.schema,
+        })
+    return error_descriptions if len(error_descriptions) else None
+
+
+def parse_property_warnings(data: dict, prop_name: str, property_changes: List[tuple]) -> Optional[dict]:
+    for (old_value, new_value) in property_changes:
+        value = data[prop_name]
+        property_warning = {
+                "property_name": prop_name,
+                "property_value": value,
+                "deprecated_value": old_value,
+                "suggested_replacement": new_value,
+        }
+
+        if value == old_value:
+            # Naive comparison for dicts
+            return property_warning
+
+        if isinstance(value, str) and isinstance(old_value, str):
+            # Lower case comparison for string values (JSON schema enum)
+            if value.lower() == old_value.lower():
+                return property_warning
+
+        # Only warn when necessary
+        return None
+
+
+def parse_schema_warnings(data: dict, schema: dict) -> Optional[List[dict]]:
+    """
+    Schema warnings are issued on Katsu releases that include schema changes.
+    Warnings are returned to highlight schema changes that may be the root cause of an IngestionError.
+
+    Parameters:
+        data (dict): the data submitted for ingestion
+
+    Returns:
+        List[dict]:
+            dict:
+                property_name (str): The name of the property
+                property_value (str | dict)
+                deprecated_value (str | dict): The deprecated property option
+                suggested_replacement (str | dict): The new suggested property option
+                version (str): The Katsu release version associated with the schema change
+    """
+    if not data or not schema:
+        return None
+
+    data_type = schema.get("$id", "").split("/")[-1]
+    applicable_changes = DATA_TYPE_SCHEMA_CHANGES.get(data_type, None)
+
+    if not applicable_changes or __version__ not in applicable_changes:
+        # Skip if data type's schema is not affected in current Katsu version
+        return None
+
+    warnings = []
+    for (version, version_changes) in applicable_changes.items():
+        for (prop_name, changes) in version_changes.get("properties", {}).items():
+            if property_warning := parse_property_warnings(data, prop_name, changes):
+                property_warning["version"] = version
+                warnings.append(property_warning)
+    return warnings if len(warnings) else None
+
+
 class IngestError(Exception):
-    pass
+
+    def __init__(self,
+                 data: dict = None,
+                 schema: dict = None,
+                 schema_validation_errors: List[ValidationError] = [],
+                 message="An error occured during ingestion."):
+
+        self.validation_errors = parse_validation_errors(schema_validation_errors)
+        self.schema_warnings = parse_schema_warnings(data=data, schema=schema)
+        self.message = message
diff --git a/chord_metadata_service/chord/ingest/experiments.py b/chord_metadata_service/chord/ingest/experiments.py
index 4fbcd60a9..c852840ee 100644
--- a/chord_metadata_service/chord/ingest/experiments.py
+++ b/chord_metadata_service/chord/ingest/experiments.py
@@ -4,7 +4,8 @@
 
 from chord_metadata_service.chord.models import Dataset
 from chord_metadata_service.experiments import models as em
-from chord_metadata_service.experiments.schemas import EXPERIMENT_SCHEMA, EXPERIMENT_RESULT_SCHEMA
+from chord_metadata_service.experiments.schemas import EXPERIMENT_SCHEMA, \
+    EXPERIMENT_RESULT_SCHEMA, EXPERIMENT_WORKFLOW_SCHEMA
 from chord_metadata_service.phenopackets import models as pm
 
 from typing import Optional
@@ -56,12 +57,24 @@ def create_experiment_result(er: dict) -> em.ExperimentResult:
 
 def validate_experiment(experiment_data, idx: Optional[int] = None) -> None:
     # Validate experiment data against experiments schema.
-    validation = schema_validation(experiment_data, EXPERIMENT_SCHEMA)
-    if not validation:
-        # TODO: Report more precise errors
+    if val_errors := schema_validation(experiment_data, EXPERIMENT_SCHEMA):
         raise IngestError(
-            f"Failed schema validation for experiment{(' ' + str(idx)) if idx is not None else ''} "
-            f"(check Katsu logs for more information)")
+            data=experiment_data,
+            schema=EXPERIMENT_SCHEMA,
+            schema_validation_errors=val_errors,
+            message=f"Failed schema validation for experiment{(' ' + str(idx)) if idx is not None else ''} "
+                    f"(check Katsu logs for more information)"
+        )
+
+
+def validate_experiment_workflow(json_data: dict) -> None:
+    if val_errors := schema_validation(json_data, EXPERIMENT_WORKFLOW_SCHEMA):
+        raise IngestError(
+            data=json_data,
+            schema=EXPERIMENT_WORKFLOW_SCHEMA,
+            schema_validation_errors=val_errors,
+            message="Failed schema validation for experiments ingestion workflow payload.",
+        )
 
 
 def ingest_experiment(
@@ -139,6 +152,9 @@ def ingest_experiment(
 
 
 def ingest_experiments_workflow(json_data, dataset_id: str) -> list[em.Experiment]:
+    # First, validate the workflow's json_data
+    validate_experiment_workflow(json_data)
+
     dataset = Dataset.objects.get(identifier=dataset_id)
 
     for rs in json_data.get("resources", []):
@@ -146,7 +162,7 @@ def ingest_experiments_workflow(json_data, dataset_id: str) -> list[em.Experimen
 
     exps = json_data.get("experiments", [])
 
-    # First, validate all experiments with the schema before creating anything in the database.
+    # Second, validate all experiments with the schema before creating anything in the database.
     for idx, exp in enumerate(exps):
         validate_experiment(exp, idx)
 
@@ -164,12 +180,16 @@ def ingest_derived_experiment_results(json_data: list[dict]) -> list[em.Experime
     # First, validate all experiment results with the schema before creating anything in the database.
 
     for idx, exp_result in enumerate(json_data):
-        validation = schema_validation(exp_result, EXPERIMENT_RESULT_SCHEMA)
-        if not validation:
+        val_errors = schema_validation(exp_result, EXPERIMENT_RESULT_SCHEMA)
+        if val_errors:
             # TODO: Report more precise errors
             raise IngestError(
-                f"Failed schema validation for experiment result {idx} "
-                f"(check Katsu logs for more information)")
+                data=exp_result,
+                schema=EXPERIMENT_RESULT_SCHEMA,
+                schema_validation_errors=val_errors,
+                message=f"Failed schema validation for experiment result {idx} "
+                        f"(check Katsu logs for more information)"
+            )
 
     # If everything passes, perform the actual ingestion next.
 
diff --git a/chord_metadata_service/chord/ingest/phenopackets.py b/chord_metadata_service/chord/ingest/phenopackets.py
index 03353dcd8..a978ae31a 100644
--- a/chord_metadata_service/chord/ingest/phenopackets.py
+++ b/chord_metadata_service/chord/ingest/phenopackets.py
@@ -85,12 +85,16 @@ def validate_phenopacket(phenopacket_data: dict[str, Any],
                          idx: Optional[int] = None) -> None:
     # Validate phenopacket data against phenopackets schema.
     # validation = schema_validation(phenopacket_data, PHENOPACKET_SCHEMA)
-    validation = schema_validation(phenopacket_data, schema, registry=VRS_REF_REGISTRY)
-    if not validation:
+    val_errors = schema_validation(phenopacket_data, schema, registry=VRS_REF_REGISTRY)
+    if val_errors:
         # TODO: Report more precise errors
         raise IngestError(
-            f"Failed schema validation for phenopacket{(' ' + str(idx)) if idx is not None else ''} "
-            f"(check Katsu logs for more information)")
+            data=phenopacket_data,
+            schema=PHENOPACKET_SCHEMA,
+            schema_validation_errors=val_errors,
+            message=f"Failed schema validation for phenopacket{(' ' + str(idx)) if idx is not None else ''} "
+                    f"(check Katsu logs for more information)"
+        )
 
 
 def update_or_create_subject(subject: dict) -> pm.Individual:
diff --git a/chord_metadata_service/chord/ingest/schema.py b/chord_metadata_service/chord/ingest/schema.py
index 1a6af33dd..577ad1e5a 100644
--- a/chord_metadata_service/chord/ingest/schema.py
+++ b/chord_metadata_service/chord/ingest/schema.py
@@ -24,10 +24,10 @@ def schema_validation(obj, schema, registry=None):
     try:
         validator.validate(obj, schema)
         logger.info("JSON schema validation passed.")
-        return True
+        return None
     except ValidationError:
         errors = [e for e in validator.iter_errors(obj)]
         logger.info("JSON schema validation failed.")
         for i, error in enumerate(errors, 1):
             logger.error(f"{i} Validation error in {'.'.join(str(v) for v in error.path)}: {error.message}")
-        return False
+        return errors
diff --git a/chord_metadata_service/chord/ingest/views.py b/chord_metadata_service/chord/ingest/views.py
index af06f0379..3e9f5f76d 100644
--- a/chord_metadata_service/chord/ingest/views.py
+++ b/chord_metadata_service/chord/ingest/views.py
@@ -6,11 +6,11 @@
 
 from django.core.exceptions import ValidationError
 from django.db import transaction
+from rest_framework import status
 from rest_framework.decorators import api_view, permission_classes
 from rest_framework.permissions import AllowAny
 from rest_framework.response import Response
-
-from bento_lib.responses import errors
+from typing import List
 
 from . import WORKFLOW_INGEST_FUNCTION_MAP
 from .exceptions import IngestError
@@ -23,18 +23,55 @@
 logger = logging.getLogger(__name__)
 
 
+class IngestResponseBuilder:
+
+    def __init__(self, workflow_id: str, dataset_id: str):
+        self.workflow_id = workflow_id
+        self.dataset_id = dataset_id
+        self.errors = []
+        self.warnings = []
+
+    def add_error(self, error):
+        self.errors.append(error)
+
+    def add_errors(self, errors: List):
+        self.errors.extend(errors)
+
+    def add_ingest_error(self, error: IngestError):
+        if error.validation_errors:
+            self.add_errors(error.validation_errors)
+        else:
+            self.add_error(error.message)
+
+        if error.schema_warnings:
+            self.warnings.extend(error.schema_warnings)
+
+    def as_response(self, status_code: int) -> Response:
+        body = {
+            "success": status_code < status.HTTP_400_BAD_REQUEST,
+            "warnings": self.warnings,
+            "errors": self.errors,
+        }
+        logger.info(f"Finished {self.workflow_id} ingest request for dataset {self.dataset_id}", body)
+        return Response(body, status=status_code)
+
+
 @api_view(["POST"])
 @permission_classes([AllowAny])
 def ingest_into_dataset(request, dataset_id: str, workflow_id: str):
     logger.info(f"Received a {workflow_id} ingest request for dataset {dataset_id}.")
 
+    response_builder = IngestResponseBuilder(workflow_id=workflow_id, dataset_id=dataset_id)
+
     # Check that the workflow exists
     if workflow_id not in WORKFLOW_INGEST_FUNCTION_MAP:
-        return Response(errors.bad_request_error(f"Ingestion workflow ID {workflow_id} does not exist"), status=400)
+        response_builder.add_error(f"Ingestion workflow ID {workflow_id} does not exist")
+        return response_builder.as_response(status.HTTP_400_BAD_REQUEST)
 
     if dataset_id not in DATASET_ID_OVERRIDES:
         if not Dataset.objects.filter(identifier=dataset_id).exists():
-            return Response(errors.bad_request_error(f"Dataset with ID {dataset_id} does not exist"), status=400)
+            response_builder.add_error(f"Dataset with ID {dataset_id} does not exist")
+            return response_builder.as_response(status.HTTP_400_BAD_REQUEST)
         dataset_id = str(uuid.UUID(dataset_id))  # Normalize dataset ID to UUID's str format.
 
     try:
@@ -43,17 +80,17 @@ def ingest_into_dataset(request, dataset_id: str, workflow_id: str):
             WORKFLOW_INGEST_FUNCTION_MAP[workflow_id](request.data, dataset_id)
 
     except IngestError as e:
-        return Response(errors.bad_request_error(f"Encountered ingest error: {e}"), status=400)
+        response_builder.add_ingest_error(e)
+        return response_builder.as_response(status.HTTP_400_BAD_REQUEST)
 
     except ValidationError as e:
-        return Response(errors.bad_request_error(
-            "Encountered validation errors during ingestion",
-            *(e.error_list if hasattr(e, "error_list") else e.error_dict.items()),
-        ))
+        response_builder.add_errors(e.error_list if hasattr(e, "error_list") else e.error_dict.items())
+        return response_builder.as_response(status.HTTP_400_BAD_REQUEST)
 
     except Exception as e:
         # Encountered some other error from the ingestion attempt, return a somewhat detailed message
         logger.error(f"Encountered an exception while processing an ingest attempt:\n{traceback.format_exc()}")
-        return Response(errors.internal_server_error(f"Encountered an exception while processing an ingest attempt "
-                                                     f"(error: {repr(e)}"), status=500)
-    return Response(status=204)
+        response_builder.add_error(f"Encountered an exception while processing an ingest attempt (error: {repr(e)})")
+        return response_builder.as_response(status.HTTP_500_INTERNAL_SERVER_ERROR)
+
+    return response_builder.as_response(status.HTTP_201_CREATED)
diff --git a/chord_metadata_service/chord/tests/example_experiment.json b/chord_metadata_service/chord/tests/example_experiment.json
index 8f6868db4..e263eeca1 100644
--- a/chord_metadata_service/chord/tests/example_experiment.json
+++ b/chord_metadata_service/chord/tests/example_experiment.json
@@ -13,7 +13,7 @@
       ],
       "library_strategy": "ChIP-Seq",
       "library_source": "Genomic",
-      "library_selection": "Random",
+      "library_selection": "RANDOM",
       "library_layout": "Single",
       "extraction_protocol": "NGS",
       "molecule": "genomic DNA",
@@ -75,4 +75,4 @@
       "url": "http://purl.obolibrary.org/obo/so.owl"
     }
   ]
-}
\ No newline at end of file
+}
diff --git a/chord_metadata_service/chord/tests/example_experiment_bad_biosample.json b/chord_metadata_service/chord/tests/example_experiment_bad_biosample.json
index b1f051378..931f15521 100644
--- a/chord_metadata_service/chord/tests/example_experiment_bad_biosample.json
+++ b/chord_metadata_service/chord/tests/example_experiment_bad_biosample.json
@@ -13,7 +13,7 @@
       ],
       "library_strategy": "ChIP-Seq",
       "library_source": "Genomic",
-      "library_selection": "Random",
+      "library_selection": "RANDOM",
       "library_layout": "Single",
       "extraction_protocol": "NGS",
       "molecule": "genomic DNA",
@@ -75,4 +75,4 @@
       "url": "http://purl.obolibrary.org/obo/so.owl"
     }
   ]
-}
\ No newline at end of file
+}
diff --git a/chord_metadata_service/chord/tests/example_invalid_experiment.json b/chord_metadata_service/chord/tests/example_invalid_experiment.json
index 437d238cf..0e47f9b72 100644
--- a/chord_metadata_service/chord/tests/example_invalid_experiment.json
+++ b/chord_metadata_service/chord/tests/example_invalid_experiment.json
@@ -11,9 +11,9 @@
           "label": "ChIP-seq"
         }
       ],
-      "library_strategy": "ChIP-Seq",
+      "library_strategy": "WES",
       "library_source": "Genomic",
-      "library_selection": "Random",
+      "library_selection": "random",
       "library_layout": "Single",
       "extraction_protocol": "NGS",
       "molecule": "genomic DNA",
@@ -75,4 +75,4 @@
       "url": "http://purl.obolibrary.org/obo/so.owl"
     }
   ]
-}
\ No newline at end of file
+}
diff --git a/chord_metadata_service/chord/tests/test_api_ingest.py b/chord_metadata_service/chord/tests/test_api_ingest.py
index 0dc865de3..e90bc4196 100644
--- a/chord_metadata_service/chord/tests/test_api_ingest.py
+++ b/chord_metadata_service/chord/tests/test_api_ingest.py
@@ -1,10 +1,11 @@
 import json
+import uuid
 
 from django.urls import reverse
 from rest_framework import status
 from rest_framework.test import APITestCase
-
-from chord_metadata_service.restapi.tests.utils import load_local_json
+from chord_metadata_service.chord.tests.example_ingest import EXAMPLE_INGEST_EXPERIMENT, \
+    EXAMPLE_INGEST_INVALID_EXPERIMENT, EXAMPLE_INGEST_INVALID_PHENOPACKET, EXAMPLE_INGEST_PHENOPACKET
 from .constants import VALID_PROJECT_1, valid_dataset_1
 from ..workflows.metadata import workflow_set, WORKFLOW_PHENOPACKETS_JSON
 
@@ -60,14 +61,20 @@ def test_phenopackets_ingest(self):
             reverse("ingest-into-dataset", args=(self.dataset["identifier"], "phenopackets_json_invalid")),
             content_type="application/json",
         )
+        c = r.json()
         self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
 
         # No ingestion body
         r = self.client.post(
             reverse("ingest-into-dataset", args=(self.dataset["identifier"], "phenopackets_json")),
             content_type="application/json",
         )
+        c = r.json()
         self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 2)  # 2 required properties missing: 'id' and 'meta_data'
 
         # Bad ingestion body JSON
         r = self.client.post(
@@ -75,22 +82,133 @@ def test_phenopackets_ingest(self):
             content_type="application/json",
             data="\{\}\}",  # noqa: W605
         )
+        c = r.json()
         self.assertEqual(r.status_code, status.HTTP_500_INTERNAL_SERVER_ERROR)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)  # 1 required property
 
         # Invalid phenopacket JSON validation
-        invalid_phenopacket = load_local_json("example_invalid_phenopacket.json")
         r = self.client.post(
             reverse("ingest-into-dataset", args=(self.dataset["identifier"], "phenopackets_json")),
             content_type="application/json",
-            data=json.dumps(invalid_phenopacket),
+            data=json.dumps(EXAMPLE_INGEST_INVALID_PHENOPACKET),
         )
+        c = r.json()
         self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)  # missing required phenopacket ID
 
         # Success
-        valid_phenopacket = load_local_json("example_phenopacket_v2.json")
         r = self.client.post(
             reverse("ingest-into-dataset", args=(self.dataset["identifier"], "phenopackets_json")),
             content_type="application/json",
-            data=json.dumps(valid_phenopacket),
+            data=json.dumps(EXAMPLE_INGEST_PHENOPACKET),
+        )
+        c = r.json()
+        self.assertEqual(c["success"], True)
+        self.assertEqual(len(c["errors"]), 0)
+        self.assertEqual(len(c["warnings"]), 0)
+        self.assertEqual(r.status_code, status.HTTP_201_CREATED)
+
+    def test_experiments_ingest_failures(self):
+        # Invalid workflow ID
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json_invalid")),
+            content_type="application/json",
+        )
+        c = r.json()
+        self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+
+        # No ingestion body
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+        )
+        c = r.json()
+        self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+
+        # Bad ingestion body JSON
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+            data="\{\}\}",  # noqa: W605
+        )
+        c = r.json()
+        self.assertEqual(r.status_code, status.HTTP_500_INTERNAL_SERVER_ERROR)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+
+        # Invalid experiments JSON validation
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_INVALID_EXPERIMENT),
+        )
+        c = r.json()
+        self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 4)
+
+        # Two of the errors concern experiment schema changes
+        warnings = c["warnings"]
+        self.assertEqual(len(warnings), 2)
+        warned_properties = [schema_warning["property_name"] for schema_warning in warnings]
+        self.assertTrue("library_selection" in warned_properties)
+        self.assertTrue("library_strategy" in warned_properties)
+
+        # Biosample not present
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_EXPERIMENT),
+        )
+        c = r.json()
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+        self.assertEqual(r.status_code, status.HTTP_500_INTERNAL_SERVER_ERROR)
+
+        # Wrong dataset id
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(uuid.uuid4(), "experiments_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_EXPERIMENT),
+        )
+        c = r.json()
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+        self.assertEqual(r.status_code, status.HTTP_400_BAD_REQUEST)
+
+        # Missing biosample
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_EXPERIMENT),
+        )
+        c = r.json()
+        self.assertEqual(c["success"], False)
+        self.assertEqual(len(c["errors"]), 1)
+        self.assertEqual(r.status_code, status.HTTP_500_INTERNAL_SERVER_ERROR)
+
+    def test_experiment_ingest_success(self):
+        # Create the required phenopacket with a biosample first
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "phenopackets_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_PHENOPACKET),
+        )
+
+        # Ingest experiment
+        r = self.client.post(
+            reverse("ingest-into-dataset", args=(self.dataset["identifier"], "experiments_json")),
+            content_type="application/json",
+            data=json.dumps(EXAMPLE_INGEST_EXPERIMENT),
         )
-        self.assertEqual(r.status_code, status.HTTP_204_NO_CONTENT)
+        c = r.json()
+        self.assertEqual(c["success"], True)
+        self.assertEqual(len(c["errors"]), 0)
+        self.assertEqual(len(c["warnings"]), 0)
+        self.assertEqual(r.status_code, status.HTTP_201_CREATED)
diff --git a/chord_metadata_service/chord/tests/test_ingest.py b/chord_metadata_service/chord/tests/test_ingest.py
index 468505475..59f19ed17 100644
--- a/chord_metadata_service/chord/tests/test_ingest.py
+++ b/chord_metadata_service/chord/tests/test_ingest.py
@@ -170,22 +170,22 @@ def test_reingesting_updating_phenopackets_json(self):
     def test_phenopackets_validation(self):
         # check invalid phenopacket, must fail validation & validate_phenopacket must raise
 
-        validation = schema_validation(EXAMPLE_INGEST_INVALID_PHENOPACKET, PHENOPACKET_SCHEMA)
-        self.assertEqual(validation, False)
+        val_errs = schema_validation(EXAMPLE_INGEST_INVALID_PHENOPACKET, PHENOPACKET_SCHEMA)
+        self.assertTrue(len(val_errs) > 0)
         with self.assertRaises(IngestError):
             validate_phenopacket(EXAMPLE_INGEST_INVALID_PHENOPACKET)
         with self.assertRaises(IngestError):
             ingest_phenopacket(EXAMPLE_INGEST_INVALID_PHENOPACKET, "dummy", validate=True)
 
         # valid phenopacket passes validation & doesn't raise
-        validation_2 = schema_validation(EXAMPLE_INGEST_PHENOPACKET, PHENOPACKET_SCHEMA)
-        self.assertEqual(validation_2, True)
+        val_errors_2 = schema_validation(EXAMPLE_INGEST_PHENOPACKET, PHENOPACKET_SCHEMA)
+        self.assertEqual(val_errors_2, None)
         validate_phenopacket(EXAMPLE_INGEST_PHENOPACKET)
 
         # valid experiments pass validation
         for exp in EXAMPLE_INGEST_EXPERIMENT["experiments"]:
-            validation_3 = schema_validation(exp, EXPERIMENT_SCHEMA)
-            self.assertEqual(validation_3, True)
+            val_errors_3 = schema_validation(exp, EXPERIMENT_SCHEMA)
+            self.assertEqual(val_errors_3, None)
 
     def test_ingesting_experiments_json(self):
         # ingest phenopackets data in order to match to biosample ids
@@ -222,8 +222,8 @@ def test_ingesting_experiments_json(self):
     def test_ingesting_invalid_experiment_json(self):
         # check invalid experiment, must fail validation
         for exp in EXAMPLE_INGEST_INVALID_EXPERIMENT["experiments"]:
-            validation = schema_validation(exp, EXPERIMENT_SCHEMA)
-            self.assertEqual(validation, False)
+            val_errs = schema_validation(exp, EXPERIMENT_SCHEMA)
+            self.assertTrue(len(val_errs) > 0)
             with self.assertRaises(IngestError):
                 validate_experiment(exp)
             with self.assertRaises(IngestError):
@@ -231,8 +231,8 @@ def test_ingesting_invalid_experiment_json(self):
 
         # check valid experiment, must pass validation
         for exp in EXAMPLE_INGEST_EXPERIMENT["experiments"]:
-            validation_2 = schema_validation(exp, EXPERIMENT_SCHEMA)
-            self.assertEqual(validation_2, True)
+            val_errs_2 = schema_validation(exp, EXPERIMENT_SCHEMA)
+            self.assertEqual(val_errs_2, None)
 
     def test_ingesting_experiment_results_json(self):
         # ingest list of experiments
diff --git a/chord_metadata_service/chord/workflows/wdls/experiments_json.wdl b/chord_metadata_service/chord/workflows/wdls/experiments_json.wdl
index a6c7aaf47..1d77ef2fe 100644
--- a/chord_metadata_service/chord/workflows/wdls/experiments_json.wdl
+++ b/chord_metadata_service/chord/workflows/wdls/experiments_json.wdl
@@ -15,12 +15,14 @@ workflow experiments_json {
             katsu_url = katsu_url,
             project_dataset = project_dataset,
             token = access_token,
-            validate_ssl = validate_ssl
+            validate_ssl = validate_ssl,
+            # ingest_report = "~{run_dir}/ingest_report.json"
     }
 
     output {
         File stdout = ingest_task.txt_output
         File stderr = ingest_task.err_output
+        File ingest_report = ingest_task.ingest_report
     }
 }
 
@@ -30,8 +32,12 @@ task ingest_task {
         String katsu_url
         String project_dataset
         String token
+        # String ingest_report
         Boolean validate_ssl
     }
+
+    # TODO: add ingest report to outputs
+    # -o "~{ingest_report}" \
     command <<<
         dataset_id=$(python3 -c 'print("~{project_dataset}".split(":")[1])')
         RESPONSE=$(curl -X POST ~{true="" false="-k" validate_ssl} -s -w "%{http_code}" \
@@ -39,7 +45,7 @@ task ingest_task {
             -H "Authorization: Bearer ~{token}" \
             --data "@~{json_document}" \
             "~{katsu_url}/ingest/${dataset_id}/experiments_json")
-        if [[ "${RESPONSE}" != "204" ]]
+        if [[ "${RESPONSE}" != "201" ]]
         then
             echo "Error: Metadata service replied with ${RESPONSE}" 1>&2  # to stderr
             exit 1
@@ -50,5 +56,6 @@ task ingest_task {
     output {
         File txt_output = stdout()
         File err_output = stderr()
+        # File ingest_report = "~{ingest_report}"
     }
 }
diff --git a/chord_metadata_service/chord/workflows/wdls/phenopackets_json.wdl b/chord_metadata_service/chord/workflows/wdls/phenopackets_json.wdl
index f281868ec..6d2a3e18f 100644
--- a/chord_metadata_service/chord/workflows/wdls/phenopackets_json.wdl
+++ b/chord_metadata_service/chord/workflows/wdls/phenopackets_json.wdl
@@ -15,6 +15,7 @@ workflow phenopackets_json {
             katsu_url = katsu_url,
             project_dataset = project_dataset,
             token = access_token,
+            # ingest_report = "~{run_dir}/ingest_report.json",
             validate_ssl = validate_ssl
     }
 
@@ -30,8 +31,12 @@ task ingest_task {
         String katsu_url
         String project_dataset
         String token
+        # String ingest_report
         Boolean validate_ssl
     }
+
+    # TODO: add ingest report to outputs
+    # -o "~{ingest_report}" \
     command <<<
         dataset_id=$(python3 -c 'print("~{project_dataset}".split(":")[1])')
         RESPONSE=$(curl -X POST ~{true="" false="-k" validate_ssl} -s -w "%{http_code}" \
@@ -39,7 +44,7 @@ task ingest_task {
             -H "Authorization: Bearer ~{token}" \
             --data "@~{json_document}" \
             "~{katsu_url}/ingest/${dataset_id}/phenopackets_json")
-        if [[ "${RESPONSE}" != "204" ]]
+        if [[ "${RESPONSE}" != "201" ]]
         then
             echo "Error: Metadata service replied with ${RESPONSE}" 1>&2  # to stderr
             exit 1
@@ -50,5 +55,6 @@ task ingest_task {
     output {
         File txt_output = stdout()
         File err_output = stderr()
+        # File ingest_report = "~{ingest_report}"
     }
 }
diff --git a/chord_metadata_service/experiments/migrations/0010_v6_2_0.py b/chord_metadata_service/experiments/migrations/0010_v6_2_0.py
new file mode 100644
index 000000000..c8754cc66
--- /dev/null
+++ b/chord_metadata_service/experiments/migrations/0010_v6_2_0.py
@@ -0,0 +1,32 @@
+from typing import List, Tuple
+from django.db import migrations
+from chord_metadata_service.experiments.schemas import EXPERIMENT_SCHEMA_CHANGES
+
+V6_2_0_PROPERTIES = EXPERIMENT_SCHEMA_CHANGES["6.2.0"]["properties"]
+LIB_STRATEGY_CONVERSIONS = V6_2_0_PROPERTIES["library_strategy"]
+LIB_SELECTION_CONVERIONS = V6_2_0_PROPERTIES["library_selection"]
+
+
+def set_experiment_library(apps, _schema_editor):
+    Experiment = apps.get_model("experiments", "Experiment")
+    for (old_val, new_val) in LIB_STRATEGY_CONVERSIONS:
+        # Modify library_strategy if necessary
+        for exp in Experiment.objects.filter(library_strategy=old_val):
+            exp.library_strategy = new_val
+            exp.save()
+
+    for (old_val, new_val) in LIB_SELECTION_CONVERIONS:
+        # Modify library_selection if necessary
+        for exp in Experiment.objects.filter(library_selection=old_val):
+            exp.library_selection = new_val
+            exp.save()
+
+
+class Migration(migrations.Migration):
+    dependencies = [
+        ('experiments', '0009_v6_0_0'),
+    ]
+
+    operations = [
+        migrations.RunPython(set_experiment_library)
+    ]
diff --git a/chord_metadata_service/experiments/schemas.py b/chord_metadata_service/experiments/schemas.py
index cefd88049..92b780ea0 100644
--- a/chord_metadata_service/experiments/schemas.py
+++ b/chord_metadata_service/experiments/schemas.py
@@ -2,11 +2,27 @@
 from .descriptions import EXPERIMENT, EXPERIMENT_RESULT, INSTRUMENT
 from chord_metadata_service.restapi.schemas import ONTOLOGY_CLASS_LIST, KEY_VALUE_OBJECT
 from chord_metadata_service.restapi.schema_utils import tag_ids_and_describe, get_schema_app_id, sub_schema_uri
+from chord_metadata_service.ontologies import read_xsd_simple_type_values, SRA_EXPERIMENT_FILE_NAME
 
 __all__ = ["EXPERIMENT_SCHEMA", "EXPERIMENT_RESULT_SCHEMA", "INSTRUMENT_SCHEMA"]
 
+
 base_uri = get_schema_app_id(Path(__file__).parent.name)
 
+# Experiment library strategy options are read from the EBI xsd file
+LIBRARY_STRATEGIES = read_xsd_simple_type_values(
+    SRA_EXPERIMENT_FILE_NAME,
+    "typeLibraryStrategy",
+)
+
+
+# Experiment library selection options are read from the EBI xsd file
+LIBRARY_SELECTION = read_xsd_simple_type_values(
+    SRA_EXPERIMENT_FILE_NAME,
+    "typeLibrarySelection",
+)
+
+
 EXPERIMENT_RESULT_SCHEMA = tag_ids_and_describe({
     "$schema": "http://json-schema.org/draft-07/schema#",
     "$id": sub_schema_uri(base_uri, "experiment_result"),
@@ -105,7 +121,7 @@
         "molecule_ontology": ONTOLOGY_CLASS_LIST,
         "library_strategy": {
             "type": "string",
-            "enum": ["Bisulfite-Seq", "RNA-Seq", "ChIP-Seq", "WES", "WGS", "RAD-Seq", "AMPLICON", "Other"]
+            "enum": LIBRARY_STRATEGIES
         },
         "library_source": {
             "type": "string",
@@ -114,7 +130,7 @@
         },
         "library_selection": {
             "type": "string",
-            "enum": ["Random", "PCR", "Random PCR", "RT-PCR", "MF", "Exome capture", "Other"]
+            "enum": LIBRARY_SELECTION
         },
         "library_layout": {
             "type": "string",
@@ -144,3 +160,45 @@
     },
     "required": ["id", "experiment_type"]
 }, EXPERIMENT)
+
+
+EXPERIMENT_WORKFLOW_SCHEMA = {
+    "$schema": "http://json-schema.org/draft-07/schema#",
+    "$id": "katsu:experiments:experiment_workflow_schema",
+    "title": "Experiment workflow schema",
+    "description": "Schema that describes the shape \
+        of an experiment workflow ingestion",
+    "type": "object",
+    "properties": {
+        "experiments": {
+            "type": "array",
+            "items": {"type": "object"},
+            "minItems": 1,
+        },
+        "resources": {
+            "type": "array",
+            "items": {"type": "object"},
+        }
+    },
+    "required": ["experiments"]
+}
+
+"""
+Dictionary of schema changes for warnings.
+"""
+EXPERIMENT_SCHEMA_CHANGES = {
+    "6.2.0": {
+        "properties": {
+            "library_strategy": [
+                    ("WES", "WXS"),
+                    ("Other", "OTHER"),
+            ],
+            "library_selection": [
+                    ("Random", "RANDOM"),
+                    ("Random PCR", "RANDOM PCR"),
+                    ("Exome capture", "Hybrid Selection"),
+                    ("Other", "other"),
+            ]
+        }
+    }
+}
diff --git a/chord_metadata_service/experiments/tests/example_experiments.json b/chord_metadata_service/experiments/tests/example_experiments.json
index e888df91b..a36023f59 100644
--- a/chord_metadata_service/experiments/tests/example_experiments.json
+++ b/chord_metadata_service/experiments/tests/example_experiments.json
@@ -13,7 +13,7 @@
       ],
       "library_strategy": "ChIP-Seq",
       "library_source": "Genomic",
-      "library_selection": "Random",
+      "library_selection": "RANDOM",
       "library_layout": "Single",
       "extraction_protocol": "NGS",
       "molecule": "genomic DNA",
@@ -77,7 +77,7 @@
       ],
       "library_strategy": "ChIP-Seq",
       "library_source": "Genomic",
-      "library_selection": "Random",
+      "library_selection": "RANDOM",
       "library_layout": "Single",
       "extraction_protocol": "NGS",
       "molecule": "genomic DNA",
@@ -139,4 +139,4 @@
       "url": "http://purl.obolibrary.org/obo/so.owl"
     }
   ]
-}
\ No newline at end of file
+}
diff --git a/chord_metadata_service/ontologies/__init__.py b/chord_metadata_service/ontologies/__init__.py
new file mode 100644
index 000000000..b05e2bc07
--- /dev/null
+++ b/chord_metadata_service/ontologies/__init__.py
@@ -0,0 +1,6 @@
+from .utils import read_xsd_simple_type_values, SRA_EXPERIMENT_FILE_NAME
+
+__all__ = [
+    "read_xsd_simple_type_values",
+    "SRA_EXPERIMENT_FILE_NAME",
+]
diff --git a/chord_metadata_service/ontologies/utils.py b/chord_metadata_service/ontologies/utils.py
new file mode 100644
index 000000000..36a28e9f8
--- /dev/null
+++ b/chord_metadata_service/ontologies/utils.py
@@ -0,0 +1,23 @@
+import os
+from typing import List
+import xmltodict
+from pathlib import Path
+
+XSD_ONTOLOGIES_PATH = Path("chord_metadata_service/ontologies/xsd/")
+SRA_EXPERIMENT_FILE_NAME = "SRA.experiment.xsd.xml"
+
+
+def read_xsd_simple_type_values(xsd_file_name: str, type_name: str) -> List[str]:
+    """Reads an XML Schema Definition (XSD) file and returns a type's values.
+    The XSD file is parsed using xmltodict following this spec:
+    https://www.xml.com/pub/a/2006/05/31/converting-between-xml-and-json.html
+    """
+    xsd_file_path = os.path.join(XSD_ONTOLOGIES_PATH, xsd_file_name)
+    with open(xsd_file_path, "r") as file:
+        xsd_file = file.read()
+
+    xsd_data = xmltodict.parse(xsd_file, namespaces={"xs": None})
+    simple_types = {sp["@name"]: sp for sp in xsd_data["schema"]["simpleType"]}
+    target_type = simple_types[type_name]
+    values = [val["@value"] for val in target_type["restriction"]["enumeration"]]
+    return values
diff --git a/chord_metadata_service/ontologies/xsd/SRA.experiment.xsd.xml b/chord_metadata_service/ontologies/xsd/SRA.experiment.xsd.xml
new file mode 100644
index 000000000..64d4931fa
--- /dev/null
+++ b/chord_metadata_service/ontologies/xsd/SRA.experiment.xsd.xml
@@ -0,0 +1,799 @@
+<?xml version="1.0" encoding="UTF-8"?>
+<!--
+  ~ Copyright 2018 EMBL - European Bioinformatics Institute
+  ~ Licensed under the Apache License, Version 2.0 (the "License"); you may not use this
+  ~ file except in compliance with the License. You may obtain a copy of the License at
+  ~ http://www.apache.org/licenses/LICENSE-2.0
+  ~ Unless required by applicable law or agreed to in writing, software distributed under the
+  ~ License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR
+  ~ CONDITIONS OF ANY KIND, either express or implied. See the License for the
+  ~ specific language governing permissions and limitations under the License.
+  -->
+<xs:schema xmlns:xs="http://www.w3.org/2001/XMLSchema" xmlns:com="SRA.common">
+  <xs:import schemaLocation="SRA.common.xsd" namespace="SRA.common"/>
+
+  <!-- STRING ENUMERATIONS BEGIN -->
+  <xs:simpleType name="typeLibraryStrategy">
+    <xs:annotation>
+      <xs:documentation>Sequencing technique intended for this library.</xs:documentation>
+    </xs:annotation>
+    <xs:restriction base="xs:string">
+      <xs:enumeration value="WGS">
+        <xs:annotation>
+          <xs:documentation>Whole Genome Sequencing - random sequencing of the whole genome (see pubmed 10731132 for details)
+          </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="WGA">
+        <xs:annotation>
+          <xs:documentation>Whole Genome Amplification followed by random sequencing. (see pubmed 1631067,8962113 for details)
+          </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="WXS">
+        <xs:annotation>
+          <xs:documentation> Random sequencing of exonic regions selected from the genome. (see pubmed 20111037 for details)
+          </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RNA-Seq">
+        <xs:annotation>
+          <xs:documentation> Random sequencing of whole transcriptome, also known as Whole Transcriptome Shotgun Sequencing, or WTSS). (see
+            pubmed 18611170 for details) </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ssRNA-seq">
+        <xs:annotation>
+          <xs:documentation> Strand-specific RNA sequencing.
+          </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="snRNA-seq">
+        <xs:annotation>
+          <xs:documentation>Single nucleus RNA sequencing is a method for profiling gene expression in cells which are difficult to isolate.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="miRNA-Seq">
+        <xs:annotation>
+          <xs:documentation> Micro RNA sequencing strategy designed to capture post-transcriptional RNA elements and include non-coding
+            functional elements. (see pubmed 21787409 for details) </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ncRNA-Seq">
+        <xs:annotation>
+          <xs:documentation>Capture of other non-coding RNA types, including post-translation modification types such as snRNA (small
+            nuclear RNA) or snoRNA (small nucleolar RNA), or expression regulation types such as siRNA (small interfering RNA) or
+            piRNA/piwi/RNA (piwi-interacting RNA).</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="FL-cDNA">
+        <xs:annotation>
+          <xs:documentation> Full-length sequencing of cDNA templates </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="EST">
+        <xs:annotation>
+          <xs:documentation> Single pass sequencing of cDNA templates </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Hi-C">
+        <xs:annotation>
+          <xs:documentation> Chromosome Conformation Capture technique where a biotin-labeled nucleotide is incorporated at the ligation junction, enabling selective purification of chimeric DNA ligation junctions followed by deep sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ATAC-seq">
+        <xs:annotation>
+          <xs:documentation> Assay for Transposase-Accessible Chromatin (ATAC) strategy is used to study genome-wide chromatin accessibility. alternative method to DNase-seq that uses an engineered Tn5 transposase to cleave DNA and to integrate primer DNA sequences into the cleaved genomic DNA. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="WCS">
+        <xs:annotation>
+          <xs:documentation> Random sequencing of a whole chromosome or other replicon isolated from a genome. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RAD-Seq"/>
+      <xs:enumeration value="CLONE">
+        <xs:annotation>
+          <xs:documentation> Genomic clone based (hierarchical) sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="POOLCLONE">
+        <xs:annotation>
+          <xs:documentation> Shotgun of pooled clones (usually BACs and Fosmids). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="AMPLICON">
+        <xs:annotation>
+          <xs:documentation> Sequencing of overlapping or distinct PCR or RT-PCR products. For example, metagenomic community profiling
+            using SSU rRNA . </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="CLONEEND">
+        <xs:annotation>
+          <xs:documentation> Clone end (5', 3', or both) sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="FINISHING">
+        <xs:annotation>
+          <xs:documentation> Sequencing intended to finish (close) gaps in existing coverage. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ChIP-Seq">
+        <xs:annotation>
+          <xs:documentation> ChIP-seq, Chromatin ImmunoPrecipitation, reveals binding sites of specific proteins, typically transcription factors (TFs) using antibodies to extract DNA fragments bound to the target protein. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MNase-Seq">
+        <xs:annotation>
+          <xs:documentation> Identifies well-positioned nucleosomes. uses Micrococcal Nuclease (MNase) is an endo-exonuclease that processively digests DNA until an obstruction, such as a nucleosome, is reached. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="DNase-Hypersensitivity">
+        <xs:annotation>
+          <xs:documentation> Sequencing of hypersensitive sites, or segments of open chromatin that are more readily cleaved by DNaseI.
+          </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Bisulfite-Seq">
+        <xs:annotation>
+          <xs:documentation>MethylC-seq. Sequencing following treatment of DNA with bisulfite to convert cytosine residues to uracil
+            depending on methylation status. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="CTS">
+        <xs:annotation>
+          <xs:documentation> Concatenated Tag Sequencing </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MRE-Seq">
+        <xs:annotation>
+          <xs:documentation> Methylation-Sensitive Restriction Enzyme Sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MeDIP-Seq">
+        <xs:annotation>
+          <xs:documentation> Methylated DNA Immunoprecipitation Sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MBD-Seq">
+        <xs:annotation>
+          <xs:documentation> Methyl CpG Binding Domain Sequencing. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Tn-Seq">
+        <xs:annotation>
+          <xs:documentation>Quantitatively determine fitness of bacterial genes based on how many times a purposely seeded transposon gets
+            inserted into each gene of a colony after some time. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="VALIDATION">
+        <xs:annotation>
+          <xs:documentation>CGHub special request: Independent experiment to re-evaluate putative variants. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="FAIRE-seq">
+        <xs:annotation>
+          <xs:documentation>Formaldehyde Assisted Isolation of Regulatory Elements. Reveals regions of open chromatin. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="SELEX">
+        <xs:annotation>
+          <xs:documentation>Systematic Evolution of Ligands by Exponential enrichment</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RIP-Seq">
+        <xs:annotation>
+          <xs:documentation>Direct sequencing of RNA immunoprecipitates (includes CLIP-Seq, HITS-CLIP and PAR-CLIP). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ChIA-PET">
+        <xs:annotation>
+          <xs:documentation>Direct sequencing of proximity-ligated chromatin immunoprecipitates.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Synthetic-Long-Read">
+        <xs:annotation>
+          <xs:documentation>binning and barcoding of large DNA fragments to facilitate assembly of the fragment</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Targeted-Capture">
+        <xs:annotation>
+          <xs:documentation>Enrichment of a targeted subset of loci.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Tethered Chromatin Conformation Capture"/>
+      <xs:enumeration value="NOMe-Seq">
+        <xs:annotation>
+          <xs:documentation>Nucleosome Occupancy and Methylome sequencing.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ChM-Seq">
+        <xs:annotation>
+          <xs:documentation>ChIPmentation combines chromatin immunoprecipitation with sequencing library preparation by Tn5 transposase (see pubmed 26280331 for details)</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="GBS">
+        <xs:annotation>
+          <xs:documentation>Genotyping by sequencing is a method to discover single nucleotide polymorphisms for genotyping studies.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Ribo-Seq">
+        <xs:annotation>
+          <xs:documentation>Ribosome profiling (also named ribosome footprinting) that uses specialized messenger RNA (mRNA) sequencing to determine which mRNAs are being actively translated. It produces a "global snapshot" of all the ribosomes active in a cell at a particular moment, known as a translatome.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="OTHER">
+        <xs:annotation>
+          <xs:documentation> Library strategy not listed. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+    </xs:restriction>
+  </xs:simpleType>
+
+  <xs:simpleType name="typeLibrarySource">
+    <xs:annotation>
+      <xs:documentation> The LIBRARY_SOURCE specifies the type of source material that is being sequenced. </xs:documentation>
+    </xs:annotation>
+    <xs:restriction base="xs:string">
+      <xs:enumeration value="GENOMIC">
+        <xs:annotation>
+          <xs:documentation> Genomic DNA (includes PCR products from genomic DNA). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="GENOMIC SINGLE CELL"/>
+      <xs:enumeration value="TRANSCRIPTOMIC">
+        <xs:annotation>
+          <xs:documentation> Transcription products or non genomic DNA (EST, cDNA, RT-PCR, screened libraries). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="TRANSCRIPTOMIC SINGLE CELL"/>
+      <xs:enumeration value="METAGENOMIC">
+        <xs:annotation>
+          <xs:documentation> Mixed material from metagenome. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="METATRANSCRIPTOMIC">
+        <xs:annotation>
+          <xs:documentation> Transcription products from community targets </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="SYNTHETIC">
+        <xs:annotation>
+          <xs:documentation> Synthetic DNA. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="VIRAL RNA">
+        <xs:annotation>
+          <xs:documentation> Viral RNA. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="OTHER">
+        <xs:annotation>
+          <xs:documentation> Other, unspecified, or unknown library source material. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+    </xs:restriction>
+  </xs:simpleType>
+
+  <xs:simpleType name="typeLibrarySelection">
+    <xs:annotation>
+      <xs:documentation> Method used to enrich the target in the sequence library preparation </xs:documentation>
+    </xs:annotation>
+    <xs:restriction base="xs:string">
+      <xs:enumeration value="RANDOM">
+        <xs:annotation>
+          <xs:documentation>No Selection or Random selection</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="PCR">
+        <xs:annotation>
+          <xs:documentation>target enrichment via PCR</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RANDOM PCR">
+        <xs:annotation>
+          <xs:documentation>Source material was selected by randomly generated primers.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RT-PCR">
+        <xs:annotation>
+          <xs:documentation>target enrichment via </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="HMPR">
+        <xs:annotation>
+          <xs:documentation>Hypo-methylated partial restriction digest</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MF">
+        <xs:annotation>
+          <xs:documentation>Methyl Filtrated</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="repeat fractionation">
+        <xs:annotation>
+          <xs:documentation>Selection for less repetitive (and more gene rich) sequence through Cot filtration (CF) or other fractionation
+            techniques based on DNA kinetics. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="size fractionation">
+        <xs:annotation>
+          <xs:documentation> Physical selection of size appropriate targets. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MSLL">
+        <xs:annotation>
+          <xs:documentation>Methylation Spanning Linking Library</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="cDNA">
+        <xs:annotation>
+          <xs:documentation>PolyA selection or enrichment for messenger RNA (mRNA); synonymize with PolyA </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="cDNA_randomPriming"/>
+      <xs:enumeration value="cDNA_oligo_dT"/>
+      <xs:enumeration value="PolyA">
+        <xs:annotation>
+          <xs:documentation>PolyA selection or enrichment for messenger RNA (mRNA); should replace cDNA enumeration. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Oligo-dT">
+        <xs:annotation>
+          <xs:documentation>enrichment of messenger RNA (mRNA) by hybridization to Oligo-dT. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Inverse rRNA">
+        <xs:annotation>
+          <xs:documentation>depletion of ribosomal RNA by oligo hybridization. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Inverse rRNA selection">
+        <xs:annotation>
+          <xs:documentation>depletion of ribosomal RNA by inverse oligo hybridization. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ChIP">
+        <xs:annotation>
+          <xs:documentation>Chromatin immunoprecipitation</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="ChIP-Seq">
+        <xs:annotation>
+        <xs:documentation>Chromatin immunoPrecipitation, reveals binding sites of specific proteins, typically transcription factors (TFs) using antibodies to extract DNA fragments bound to the target protein.</xs:documentation>
+      </xs:annotation>
+    </xs:enumeration>
+      <xs:enumeration value="MNase">
+        <xs:annotation>
+          <xs:documentation>Identifies well-positioned nucleosomes. uses Micrococcal Nuclease (MNase) is an endo-exonuclease that processively digests DNA until an obstruction, such as a nucleosome, is reached.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="DNase">
+        <xs:annotation>
+          <xs:documentation>DNase I endonuclease digestion and size selection reveals regions of chromatin where the DNA is highly sensitive to DNase I.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Hybrid Selection">
+        <xs:annotation>
+          <xs:documentation>Selection by hybridization in array or solution.</xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Reduced Representation">
+        <xs:annotation>
+          <xs:documentation>Reproducible genomic subsets, often generated by restriction fragment size selection, containing a manageable
+            number of loci to facilitate re-sampling. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="Restriction Digest">
+        <xs:annotation>
+          <xs:documentation> DNA fractionation using restriction enzymes. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="5-methylcytidine antibody">
+        <xs:annotation>
+          <xs:documentation> Selection of methylated DNA fragments using an antibody raised against 5-methylcytosine or 5-methylcytidine
+            (m5C). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MBD2 protein methyl-CpG binding domain">
+        <xs:annotation>
+          <xs:documentation> Enrichment by methyl-CpG binding domain. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="CAGE">
+        <xs:annotation>
+          <xs:documentation> Cap-analysis gene expression. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="RACE">
+        <xs:annotation>
+          <xs:documentation> Rapid Amplification of cDNA Ends. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="MDA">
+        <xs:annotation>
+          <xs:documentation> Multiple Displacement Amplification, a non-PCR based DNA amplification technique that amplifies a minute
+            quantifies of DNA to levels suitable for genomic analysis. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="padlock probes capture method">
+        <xs:annotation>
+          <xs:documentation> Targeted sequence capture protocol covering an arbitrary set of nonrepetitive genomics targets. An example is
+            capture bisulfite sequencing using padlock probes (BSPP). </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="other">
+        <xs:annotation>
+          <xs:documentation> Other library enrichment, screening, or selection process. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+      <xs:enumeration value="unspecified">
+        <xs:annotation>
+          <xs:documentation> Library enrichment, screening, or selection is not specified. </xs:documentation>
+        </xs:annotation>
+      </xs:enumeration>
+    </xs:restriction>
+  </xs:simpleType>
+  <!-- STRING ENUMERATIONS END -->
+
+
+  <xs:complexType name="PoolMemberType">
+    <xs:complexContent>
+      <xs:extension base="com:RefObjectType">
+        <xs:sequence>
+          <xs:element name="READ_LABEL" minOccurs="0" maxOccurs="unbounded">
+            <xs:complexType>
+              <xs:simpleContent>
+                <xs:extension base="xs:string">
+                  <xs:attribute name="read_group_tag" type="xs:string">
+                    <xs:annotation>
+                      <xs:documentation> Assignment of read_group_tag to decoded read </xs:documentation>
+                    </xs:annotation>
+                  </xs:attribute>
+                </xs:extension>
+              </xs:simpleContent>
+            </xs:complexType>
+          </xs:element>
+        </xs:sequence>
+        <xs:attribute name="member_name" type="xs:string" use="optional">
+          <xs:annotation>
+            <xs:documentation> Label a sample within a scope of the pool </xs:documentation>
+          </xs:annotation>
+        </xs:attribute>
+        <xs:attribute name="proportion" type="xs:float" use="optional">
+          <xs:annotation>
+            <xs:documentation> Proportion of this sample (in percent) that was included in sample pool. </xs:documentation>
+          </xs:annotation>
+        </xs:attribute>
+      </xs:extension>
+    </xs:complexContent>
+  </xs:complexType>
+  <xs:complexType name="SampleDescriptorType">
+    <xs:complexContent>
+      <xs:extension base="com:RefObjectType">
+        <xs:choice minOccurs="0" maxOccurs="1">
+          <xs:element name="POOL">
+            <xs:annotation>
+              <xs:documentation>
+            Identifies a list of group/pool/multiplex sample members.  This implies that
+            this sample record is a group, pool, or multiplex, but it continues to receive
+            its own accession and can be referenced by an experiment.  By default if
+            no match to any of the listed members can be determined, then the default
+            sample reference is used.
+          </xs:documentation>
+            </xs:annotation>
+            <xs:complexType>
+              <xs:sequence>
+                <xs:element name="DEFAULT_MEMBER" type="PoolMemberType" minOccurs="0" maxOccurs="1">
+                  <xs:annotation>
+                    <xs:documentation> Reference to the sample that is used when read membership cannot be determined. A default member should
+                  be provided if there exists a possibility that some reads will be left over from barcode/MID resolution. A default member
+                  is not needed when defining a true pool (where individual samples are not distinguished in the reads), or the reads have
+                  been partitioned among the pool members (no leftovers). </xs:documentation>
+                  </xs:annotation>
+                </xs:element>
+                <xs:element name="MEMBER" type="PoolMemberType" minOccurs="1" maxOccurs="unbounded">
+                  <xs:annotation>
+                    <xs:documentation> Reference to the sample as determined from barcode/MID resolution or read partition. </xs:documentation>
+                  </xs:annotation>
+                </xs:element>
+              </xs:sequence>
+            </xs:complexType>
+          </xs:element>
+        </xs:choice>
+      </xs:extension>
+    </xs:complexContent>
+  </xs:complexType>
+  <xs:complexType name="LibraryDescriptorType">
+    <xs:annotation>
+      <xs:documentation> The LIBRARY_DESCRIPTOR specifies the origin of the material being
+        sequenced and any treatments that the material might have undergone that affect the
+        sequencing result. This specification is needed even if the platform does not
+        require a library construction step per se. </xs:documentation>
+    </xs:annotation>
+    <xs:sequence>
+      <xs:element name="LIBRARY_NAME" type="xs:string" maxOccurs="1" minOccurs="0">
+        <xs:annotation>
+          <xs:documentation>
+            The submitter's name for this library.
+          </xs:documentation>
+        </xs:annotation>
+      </xs:element>
+      <xs:element name="LIBRARY_STRATEGY" type="typeLibraryStrategy" minOccurs="1" maxOccurs="1"/>
+      <xs:element name="LIBRARY_SOURCE" type="typeLibrarySource" minOccurs="1" maxOccurs="1"/>
+      <xs:element name="LIBRARY_SELECTION" type="typeLibrarySelection" minOccurs="1" maxOccurs="1"/>
+      <xs:element name="LIBRARY_LAYOUT">
+        <xs:annotation>
+          <xs:documentation>
+            LIBRARY_LAYOUT specifies whether to expect single, paired, or other configuration of reads.
+            In the case of paired reads, information about the relative distance and orientation is specified.
+          </xs:documentation>
+        </xs:annotation>
+        <xs:complexType>
+          <xs:choice>
+            <xs:element name="SINGLE">
+              <xs:complexType>
+                <xs:annotation>
+                  <xs:documentation>
+                    Reads are unpaired (usual case).
+                  </xs:documentation>
+                </xs:annotation>
+              </xs:complexType>
+            </xs:element>
+            <xs:element name="PAIRED">
+              <xs:complexType>
+                <xs:attribute name="NOMINAL_LENGTH" type="xs:nonNegativeInteger"/>
+                <xs:attribute name="NOMINAL_SDEV" type="xs:double"/>
+              </xs:complexType>
+            </xs:element>
+          </xs:choice>
+        </xs:complexType>
+      </xs:element>
+      <xs:element name="TARGETED_LOCI" minOccurs="0" maxOccurs="1">
+        <xs:complexType>
+          <xs:annotation>
+            <xs:documentation>
+              Names the gene(s) or locus(loci) or other genomic feature(s) targeted by the sequence.
+            </xs:documentation>
+          </xs:annotation>
+          <xs:sequence>
+            <xs:element name="LOCUS" maxOccurs="unbounded" minOccurs="1">
+              <xs:complexType>
+                <xs:sequence>
+                  <xs:element name="PROBE_SET" type="com:XRefType" maxOccurs="1" minOccurs="0">
+                    <xs:annotation>
+                      <xs:documentation> Reference to an archived primer or
+                        probe set. Example: dbProbe </xs:documentation>
+                    </xs:annotation>
+                  </xs:element>
+                </xs:sequence>
+                <xs:attribute name="locus_name">
+                  <xs:simpleType>
+                    <xs:restriction base="xs:string">
+                      <xs:enumeration value="16S rRNA">
+                        <xs:annotation>
+                          <xs:documentation> Bacterial small subunit ribosomal RNA, a locus used for
+                            phylogenetic studies of bacteria and as a target for random target PCR in
+                            environmental biodiversity screening. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="18S rRNA">
+                        <xs:annotation>
+                          <xs:documentation> Eukaryotic small subunit ribosomal RNA, a locus used for
+                            phylogenetic studies of eukaryotes and as a target for random target PCR in
+                            environmental biodiversity screening. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="28S rRNA">
+                        <xs:annotation>
+                          <xs:documentation>Structural ribosomal RNA for the large component, or large
+                            subunit (LSU) of eukaryotic cytoplasmic ribosomes.. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="RBCL">
+                        <xs:annotation>
+                          <xs:documentation> RuBisCO large subunit : ribulose-1,5-bisphosphate
+                            carboxylase/oxygenase large subunit, a locus used for phylogenetic studies
+                            of plants. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="matK">
+                        <xs:annotation>
+                          <xs:documentation> Maturase K gene, a locus used for phylogenetic studies of
+                            plants. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="COX1">
+                        <xs:annotation>
+                          <xs:documentation> Mitochondrial cytochrome c oxidase 1 gene, a locus used for
+                            phylogenetic studies of animals </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="ITS1-5.8S-ITS2">
+                        <xs:annotation>
+                          <xs:documentation> Internal transcribed spacers 1 and 2 plus 5.8S rRNA region,
+                            a locus used for phylogenetic studies of fungi. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="exome">
+                        <xs:annotation>
+                          <xs:documentation> All exonic regions of the genome. </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                      <xs:enumeration value="other">
+                        <xs:annotation>
+                          <xs:documentation> Other locus, please describe.
+                          </xs:documentation>
+                        </xs:annotation>
+                      </xs:enumeration>
+                    </xs:restriction>
+                  </xs:simpleType>
+                </xs:attribute>
+                <xs:attribute name="description" type="xs:string">
+                  <xs:annotation>
+                    <xs:documentation> Submitter supplied description of alternate locus and auxiliary
+                      information. </xs:documentation>
+                  </xs:annotation>
+                </xs:attribute>
+              </xs:complexType>
+            </xs:element>
+
+          </xs:sequence>
+
+
+        </xs:complexType>
+      </xs:element>
+      <xs:element name="POOLING_STRATEGY" minOccurs="0" maxOccurs="1">
+        <xs:annotation>
+          <xs:documentation>
+            The optional pooling strategy indicates how the library or libraries are organized if multiple samples are involved.
+          </xs:documentation>
+        </xs:annotation>
+        <xs:simpleType>
+          <xs:restriction base="xs:string"> </xs:restriction>
+        </xs:simpleType>
+      </xs:element>
+      <xs:element name="LIBRARY_CONSTRUCTION_PROTOCOL" type="xs:string" minOccurs="0" maxOccurs="1">
+        <xs:annotation>
+          <xs:documentation>
+            Free form text describing the protocol by which the sequencing library was constructed.
+          </xs:documentation>
+        </xs:annotation>
+      </xs:element>
+    </xs:sequence>
+  </xs:complexType>
+  <xs:complexType name="LibraryType">
+    <xs:sequence>
+      <xs:element name="DESIGN_DESCRIPTION" type="xs:string">
+        <xs:annotation>
+          <xs:documentation>Goal and setup of the individual library including library was constructed.</xs:documentation>
+        </xs:annotation>
+      </xs:element>
+
+      <xs:element name="SAMPLE_DESCRIPTOR" type="SampleDescriptorType">
+        <xs:annotation>
+          <xs:documentation> Pick a sample to associate this experiment with. The sample may be an individual or a pool,
+            depending on how it is specified. </xs:documentation>
+        </xs:annotation>
+      </xs:element>
+
+      <xs:element name="LIBRARY_DESCRIPTOR" type="LibraryDescriptorType">
+        <xs:annotation>
+          <xs:documentation> The LIBRARY_DESCRIPTOR specifies the origin of the material being sequenced and any
+            treatments that the material might have undergone that affect the sequencing result. This specification is
+            needed even if the platform does not require a library construction step per se. </xs:documentation>
+        </xs:annotation>
+      </xs:element>
+
+      <xs:element name="SPOT_DESCRIPTOR" type="com:SpotDescriptorType" minOccurs="0" maxOccurs="1">
+        <xs:annotation>
+          <xs:documentation> The SPOT_DESCRIPTOR specifies how to decode the individual reads of interest from the
+            monolithic spot sequence. The spot descriptor contains aspects of the experimental design, platform, and
+            processing information. There will be two methods of specification: one will be an index into a table of
+            typical decodings, the other being an exact specification. This construct is needed for loading data and for
+            interpreting the loaded runs. It can be omitted if the loader can infer read layout (from multiple input
+            files or from one input files). </xs:documentation>
+        </xs:annotation>
+      </xs:element>
+    </xs:sequence>
+
+  </xs:complexType>
+
+  <xs:complexType name="ExperimentType">
+
+    <xs:annotation>
+      <xs:documentation>
+        An Experiment specifies of what will be sequenced and how the sequencing will be performed.
+        It does not contain results.
+        An Experiment is composed of a design, a platform selection, and processing parameters.
+      </xs:documentation>
+    </xs:annotation>
+
+    <xs:complexContent>
+      <xs:extension base="com:ObjectType">
+        <xs:sequence>
+          <xs:element name="TITLE" type="xs:string" minOccurs="0" maxOccurs="1">
+            <xs:annotation>
+              <xs:documentation>
+            Short text that can be used to call out experiment records in searches or in displays.
+            This element is technically optional but should be used for all new records.
+          </xs:documentation>
+            </xs:annotation>
+          </xs:element>
+          <xs:element name="STUDY_REF" minOccurs="1" maxOccurs="1">
+            <xs:annotation>
+              <xs:documentation>
+            Identifies the parent study.
+          </xs:documentation>
+            </xs:annotation>
+            <xs:complexType>
+              <xs:complexContent>
+                <xs:extension base="com:RefObjectType"> </xs:extension>
+              </xs:complexContent>
+            </xs:complexType>
+          </xs:element>
+          <xs:element name="DESIGN" type="LibraryType" maxOccurs="1" minOccurs="1">
+            <xs:annotation>
+              <xs:documentation> The library design including library properties, layout, protocol, targeting information, and spot and gap
+            descriptors. </xs:documentation>
+            </xs:annotation>
+          </xs:element>
+          <xs:element name="PLATFORM" type="com:PlatformType" maxOccurs="1" minOccurs="1">
+            <xs:annotation>
+              <xs:documentation>
+            The PLATFORM record selects which sequencing platform and platform-specific runtime parameters.
+            This will be determined by the Center.
+          </xs:documentation>
+            </xs:annotation>
+          </xs:element>
+
+          <xs:element name="PROCESSING" type="com:ProcessingType" minOccurs="0" maxOccurs="1"/>
+
+          <xs:element name="EXPERIMENT_LINKS" minOccurs="0" maxOccurs="1">
+            <xs:annotation>
+              <xs:documentation>
+            Links to resources related to this experiment or experiment set (publication, datasets, online databases).
+          </xs:documentation>
+            </xs:annotation>
+            <xs:complexType>
+              <xs:sequence minOccurs="1" maxOccurs="unbounded">
+                <xs:element name="EXPERIMENT_LINK" type="com:LinkType"/>
+              </xs:sequence>
+            </xs:complexType>
+          </xs:element>
+
+          <xs:element name="EXPERIMENT_ATTRIBUTES" minOccurs="0" maxOccurs="1">
+            <xs:annotation>
+              <xs:documentation>
+            Properties and attributes of the experiment.  These can be entered as free-form
+            tag-value pairs.
+          </xs:documentation>
+            </xs:annotation>
+            <xs:complexType>
+              <xs:sequence maxOccurs="unbounded" minOccurs="1">
+                <xs:element name="EXPERIMENT_ATTRIBUTE" type="com:AttributeType"/>
+              </xs:sequence>
+            </xs:complexType>
+          </xs:element>
+        </xs:sequence>
+      </xs:extension>
+    </xs:complexContent>
+  </xs:complexType>
+
+  <xs:complexType name="ExperimentSetType">
+    <xs:sequence minOccurs="1" maxOccurs="1">
+      <xs:element name="EXPERIMENT" type="ExperimentType" maxOccurs="unbounded"/>
+    </xs:sequence>
+  </xs:complexType>
+
+  <xs:element name="EXPERIMENT_SET" type="ExperimentSetType">
+    <xs:annotation>
+      <xs:documentation>
+        An EXPERMENT_SET is a container for a set of experiments and a common namespace.
+      </xs:documentation>
+    </xs:annotation>
+
+  </xs:element>
+
+  <xs:element name="EXPERIMENT" type="ExperimentType"/>
+</xs:schema>
\ No newline at end of file
diff --git a/chord_metadata_service/phenopackets/schemas.py b/chord_metadata_service/phenopackets/schemas.py
index 51be759b9..a5dc4d042 100644
--- a/chord_metadata_service/phenopackets/schemas.py
+++ b/chord_metadata_service/phenopackets/schemas.py
@@ -658,7 +658,7 @@
     "required": ["id", "meta_data"],
 }, descriptions.PHENOPACKET)
 
-VRS_REF_RESOURCE = Resource.from_contents(contents=vrs_schema_definitions, default_specification=DRAFT_07)
+VRS_REF_RESOURCE = Resource.from_contents(contents=vrs_schema_definitions)
 VRS_REF_REGISTRY = VRS_REF_RESOURCE @ Registry()
 
 resolver = VRS_REF_REGISTRY.resolver()
diff --git a/poetry.lock b/poetry.lock
index 23903b429..5e787f45c 100644
--- a/poetry.lock
+++ b/poetry.lock
@@ -2,19 +2,20 @@
 
 [[package]]
 name = "adrf"
-version = "0.1.2"
+version = "0.1.3"
 description = "Async support for Django REST framework"
 optional = false
 python-versions = ">=3.8"
 files = [
-    {file = "adrf-0.1.2-py3-none-any.whl", hash = "sha256:a33f8f51f0f80072ffb2af061df1fb119bc00adaa720a2972049d4aa33155337"},
-    {file = "adrf-0.1.2.tar.gz", hash = "sha256:ce7160878ba27999d333752941cde0687c1a205fc26fa0eda1bad3924958dc69"},
+    {file = "adrf-0.1.3-py3-none-any.whl", hash = "sha256:b848cab61d645e969261edf3fa1072411f8bfa84283fcbddd6a42b1f3ef57ce6"},
+    {file = "adrf-0.1.3.tar.gz", hash = "sha256:f76e0ff59af5359bbdd5087fae13f3ab152b6aaebb59350d5aea5e88ea588d7d"},
 ]
 
 [package.dependencies]
 async-property = ">=0.2.2"
 django = ">=4.1"
 djangorestframework = ">=3.14.0"
+isort = "5.12.0"
 
 [[package]]
 name = "aiohttp"
@@ -197,21 +198,22 @@ files = [
 
 [[package]]
 name = "attrs"
-version = "23.1.0"
+version = "23.2.0"
 description = "Classes Without Boilerplate"
 optional = false
 python-versions = ">=3.7"
 files = [
-    {file = "attrs-23.1.0-py3-none-any.whl", hash = "sha256:1f28b4522cdc2fb4256ac1a020c78acf9cba2c6b461ccd2c126f3aa8e8335d04"},
-    {file = "attrs-23.1.0.tar.gz", hash = "sha256:6279836d581513a26f1bf235f9acd333bc9115683f14f7e8fae46c98fc50e015"},
+    {file = "attrs-23.2.0-py3-none-any.whl", hash = "sha256:99b87a485a5820b23b879f04c2305b44b951b502fd64be915879d77a7e8fc6f1"},
+    {file = "attrs-23.2.0.tar.gz", hash = "sha256:935dc3b529c262f6cf76e50877d35a4bd3c1de194fd41f47a2b7ae8f19971f30"},
 ]
 
 [package.extras]
 cov = ["attrs[tests]", "coverage[toml] (>=5.3)"]
-dev = ["attrs[docs,tests]", "pre-commit"]
+dev = ["attrs[tests]", "pre-commit"]
 docs = ["furo", "myst-parser", "sphinx", "sphinx-notfound-page", "sphinxcontrib-towncrier", "towncrier", "zope-interface"]
 tests = ["attrs[tests-no-zope]", "zope-interface"]
-tests-no-zope = ["cloudpickle", "hypothesis", "mypy (>=1.1.1)", "pympler", "pytest (>=4.3.0)", "pytest-mypy-plugins", "pytest-xdist[psutil]"]
+tests-mypy = ["mypy (>=1.6)", "pytest-mypy-plugins"]
+tests-no-zope = ["attrs[tests-mypy]", "cloudpickle", "hypothesis", "pympler", "pytest (>=4.3.0)", "pytest-xdist[psutil]"]
 
 [[package]]
 name = "bento-lib"
@@ -584,24 +586,24 @@ files = [
 
 [[package]]
 name = "distlib"
-version = "0.3.7"
+version = "0.3.8"
 description = "Distribution utilities"
 optional = false
 python-versions = "*"
 files = [
-    {file = "distlib-0.3.7-py2.py3-none-any.whl", hash = "sha256:2e24928bc811348f0feb63014e97aaae3037f2cf48712d51ae61df7fd6075057"},
-    {file = "distlib-0.3.7.tar.gz", hash = "sha256:9dafe54b34a028eafd95039d5e5d4851a13734540f1331060d31c9916e7147a8"},
+    {file = "distlib-0.3.8-py2.py3-none-any.whl", hash = "sha256:034db59a0b96f8ca18035f36290806a9a6e6bd9d1ff91e45a7f172eb17e51784"},
+    {file = "distlib-0.3.8.tar.gz", hash = "sha256:1530ea13e350031b6312d8580ddb6b27a104275a31106523b8f123787f494f64"},
 ]
 
 [[package]]
 name = "django"
-version = "4.2.7"
+version = "4.2.9"
 description = "A high-level Python web framework that encourages rapid development and clean, pragmatic design."
 optional = false
 python-versions = ">=3.8"
 files = [
-    {file = "Django-4.2.7-py3-none-any.whl", hash = "sha256:e1d37c51ad26186de355cbcec16613ebdabfa9689bbade9c538835205a8abbe9"},
-    {file = "Django-4.2.7.tar.gz", hash = "sha256:8e0f1c2c2786b5c0e39fe1afce24c926040fad47c8ea8ad30aaf1188df29fc41"},
+    {file = "Django-4.2.9-py3-none-any.whl", hash = "sha256:2cc2fc7d1708ada170ddd6c99f35cc25db664f165d3794bc7723f46b2f8c8984"},
+    {file = "Django-4.2.9.tar.gz", hash = "sha256:12498cc3cb8bc8038539fef9e90e95f507502436c1f0c3a673411324fa675d14"},
 ]
 
 [package.dependencies]
@@ -790,72 +792,88 @@ files = [
 
 [[package]]
 name = "frozenlist"
-version = "1.4.0"
+version = "1.4.1"
 description = "A list-like structure which implements collections.abc.MutableSequence"
 optional = false
 python-versions = ">=3.8"
 files = [
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@@ -908,6 +926,23 @@ files = [
 [package.dependencies]
 arrow = ">=0.15.0"
 
+[[package]]
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+version = "5.12.0"
+description = "A Python utility / library to sort Python imports."
+optional = false
+python-versions = ">=3.8.0"
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+plugins = ["setuptools"]
+requirements-deprecated-finder = ["pip-api", "pipreqs"]
+
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-version = "4.8.0"
+version = "4.9.0"
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 python-versions = ">=3.8"
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 name = "tzdata"
-version = "2023.3"
+version = "2023.4"
 description = "Provider of IANA time zone data"
 optional = false
 python-versions = ">=2"
 files = [
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 [[package]]
@@ -1941,13 +1976,13 @@ zstd = ["zstandard (>=0.18.0)"]
 
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-version = "20.24.7"
+version = "20.25.0"
 description = "Virtual Python Environment builder"
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 python-versions = ">=3.7"
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 [package.dependencies]
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 [package.extras]
 watchdog = ["watchdog (>=2.3)"]
 
+[[package]]
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+version = "0.13.0"
+description = "Makes working with XML feel like you are working with JSON"
+optional = false
+python-versions = ">=3.4"
+files = [
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+]
+
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+    {file = "yarl-1.9.4-cp39-cp39-manylinux_2_17_s390x.manylinux2014_s390x.whl", hash = "sha256:e0381b4ce23ff92f8170080c97678040fc5b08da85e9e292292aba67fdac6c34"},
+    {file = "yarl-1.9.4-cp39-cp39-manylinux_2_17_x86_64.manylinux2014_x86_64.whl", hash = "sha256:23d32a2594cb5d565d358a92e151315d1b2268bc10f4610d098f96b147370136"},
+    {file = "yarl-1.9.4-cp39-cp39-manylinux_2_5_i686.manylinux1_i686.manylinux_2_17_i686.manylinux2014_i686.whl", hash = "sha256:ddb2a5c08a4eaaba605340fdee8fc08e406c56617566d9643ad8bf6852778fc7"},
+    {file = "yarl-1.9.4-cp39-cp39-musllinux_1_1_aarch64.whl", hash = "sha256:26a1dc6285e03f3cc9e839a2da83bcbf31dcb0d004c72d0730e755b33466c30e"},
+    {file = "yarl-1.9.4-cp39-cp39-musllinux_1_1_i686.whl", hash = "sha256:18580f672e44ce1238b82f7fb87d727c4a131f3a9d33a5e0e82b793362bf18b4"},
+    {file = "yarl-1.9.4-cp39-cp39-musllinux_1_1_ppc64le.whl", hash = "sha256:29e0f83f37610f173eb7e7b5562dd71467993495e568e708d99e9d1944f561ec"},
+    {file = "yarl-1.9.4-cp39-cp39-musllinux_1_1_s390x.whl", hash = "sha256:1f23e4fe1e8794f74b6027d7cf19dc25f8b63af1483d91d595d4a07eca1fb26c"},
+    {file = "yarl-1.9.4-cp39-cp39-musllinux_1_1_x86_64.whl", hash = "sha256:db8e58b9d79200c76956cefd14d5c90af54416ff5353c5bfd7cbe58818e26ef0"},
+    {file = "yarl-1.9.4-cp39-cp39-win32.whl", hash = "sha256:c7224cab95645c7ab53791022ae77a4509472613e839dab722a72abe5a684575"},
+    {file = "yarl-1.9.4-cp39-cp39-win_amd64.whl", hash = "sha256:824d6c50492add5da9374875ce72db7a0733b29c2394890aef23d533106e2b15"},
+    {file = "yarl-1.9.4-py3-none-any.whl", hash = "sha256:928cecb0ef9d5a7946eb6ff58417ad2fe9375762382f1bf5c55e61645f2c43ad"},
+    {file = "yarl-1.9.4.tar.gz", hash = "sha256:566db86717cf8080b99b58b083b773a908ae40f06681e87e589a976faf8246bf"},
 ]
 
 [package.dependencies]
@@ -2097,4 +2143,4 @@ multidict = ">=4.0"
 [metadata]
 lock-version = "2.0"
 python-versions = "^3.10.0"
-content-hash = "b0e98b5766f77250b230947c38ec2f5ae25718d6964b27b22ff149f1a2f6702a"
+content-hash = "0d662eb28b512060f129d9f2e2040ac2120a9fba2d1b132b830c6064eef84fff"
diff --git a/pyproject.toml b/pyproject.toml
index 38860abf1..3160308fa 100644
--- a/pyproject.toml
+++ b/pyproject.toml
@@ -4,7 +4,7 @@ build-backend = "poetry.core.masonry.api"
 
 [tool.poetry]
 name = "chord_metadata_service"  # can be renamed to katsu if inner module directory is renamed too
-version = "6.0.0"
+version = "6.2.0"
 description = "An implementation of a clin/pheno metadata store for the Bento platform."
 authors = [
     "Ksenia Zaytseva",
@@ -20,6 +20,7 @@ include = [
     "chord_metadata_service/chord/workflows/wdls/*.wdl",
     "chord_metadata_service/chord/tests/*.json",
     "chord_metadata_service/dats/*",
+    "chord_metadata_service/ontologies/xsd/*.xml",
     "chord_metadata_service/restapi/tests/*.json",
 ]
 repository = "https://github.com/bento-platform/katsu"
@@ -54,6 +55,7 @@ tabulate = "^0.9.0"
 uritemplate = "^4.1.1"
 pyhumps = "^3.8.0"
 adrf = "^0.1.1"
+xmltodict="0.13.0"
 
 [tool.poetry.group.dev.dependencies]
 coverage = "^6.5.0"