nim wrapper for htslib for parsing genomics data files
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Updated
Aug 27, 2024 - Nim
nim wrapper for htslib for parsing genomics data files
Python library to access Gene Expression Omnibus Database (GEO)
VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications
Sequence alignment tools
Find and visualize rearrangements in DNA sequences
Validation and manipulation of FASTQ files, scRNA-seq barcode pre-processing and UMI quantification.
Assembly of Phylogenomic Datasets from High-Throughput Sequencing data
vSNP -- validate SNPs
mGEMS Genomic epidemiology with mixed samples
A toolset for handling sequencing data with unique molecular identifiers (UMIs)
use the noise
uORF-Tools are a workflow and a collection of tools for the analysis of 'Upstream Open Reading Frames' (short uORFs)
mSWEEP High-resolution sweep metagenomics using fast probabilistic inference
Infer metadata for your downstream analysis straight from your RNA-Seq data
Bayesian modelling approach for detecting RNA flexibility changes in high-throughput structure probing data under different conditions, based on an extension of the BUM-HMM method.
Processing, quality control and analysis of GAM datsets
Sargasso disambiguates mixed-species high-throughput sequencing data.
Resolution-independent normalization of Hi-C data
vSNP -- validate SNPs
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