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docs: cleanup of documentation #621

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merged 17 commits into from
Feb 26, 2024
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# About

## The team

- Alexander Thomas
- Thomas Battenfeld
- Simon Magin
- Johannes Koester
- Folker Meyer



## Tools used in UnCoVar

This project wouldn't be possible without several open source tools and libraries:

| Tool | Link |
| -------------- | --------------------------------------------------- |
| Altair | <www.doi.org/10.21105/joss.01057> |
| BAMClipper | <www.doi.org/10.1038/s41598-017-01703-6> |
| BCFtools | <www.doi.org/10.1093/gigascience/giab008> |
| BEDTools | <www.doi.org/10.1093/bioinformatics/btq033> |
| Biopython | <www.doi.org/10.1093/bioinformatics/btp163> |
| bwa | <www.doi.org/10.1093/bioinformatics/btp324> |
| Covariants | <www.github.com/hodcroftlab/covariants> |
| delly | <www.doi.org/10.1093/bioinformatics/bts378> |
| ensembl-vep | <www.doi.org/10.1186/s13059-016-0974-4> |
| entrez-direct | <www.ncbi.nlm.nih.gov/books/NBK179288> |
| fastp | <www.doi.org/10.1093/bioinformatics/bty560> |
| FastQC | <www.bioinformatics.babraham.ac.uk/projects/fastqc> |
| fgbio | <www.github.com/fulcrum-genomics/fgbio> |
| FreeBayes | <www.arxiv.org/abs/1207.3907> |
| intervaltree | <www.github.com/chaimleib/intervaltree> |
| Jupyter | <www.jupyter.org> |
| kallisto | <www.doi.org/10.1038/nbt.3519> |
| Kraken2 | <www.doi.org/10.1186/s13059-019-1891-0> |
| Krona | <www.doi.org/10.1186/1471-2105-12-385> |
| mason | <publications.imp.fu-berlin.de/962> |
| MEGAHIT | <www.doi.org/10.1093/bioinformatics/btv033> |
| Minimap2 | <www.doi.org/10.1093/bioinformatics/bty191> |
| MultiQC | <www.doi.org/10.1093/bioinformatics/btw354> |
| pandas | <pandas.pydata.org> |
| Picard | <broadinstitute.github.io/picard> |
| PySAM | <www.doi.org/10.11578/dc.20190903.1> |
| QUAST | <www.doi.org/10.1093/bioinformatics/btt086> |
| RaGOO | <www.doi.org/10.1186/s13059-019-1829-6> |
| ruamel.yaml | <www.sourceforge.net/projects/ruamel-yaml> |
| Rust-Bio-Tools | <www.github.com/rust-bio/rust-bio-tools> |
| SAMtools | <www.doi.org/10.1093/bioinformatics/btp352> |
| Snakemake | <www.doi.org/10.12688/f1000research.29032.1> |
| sourmash | <www.doi.org/10.21105/joss.00027> |
| SPAdes | <www.doi.org/10.1089/cmb.2012.0021> |
| SVN | <www.doi.org/10.1142/s0219720005001028> |
| Tabix | <www.doi.org/10.1093/bioinformatics/btq671> |
| Trinity | <www.doi.org/10.1038/nprot.2013.084> |
| Varlociraptor | <www.doi.org/10.1186/s13059-020-01993-6> |
| Vega-Lite | <www.doi.org/10.1109/TVCG.2016.2599030> |
| Velvet | <www.doi.org/10.1101/gr.074492.107> |
| vembrane | <www.github.com/vembrane/vembrane> |
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# FAQ

## Where to find the source code?

[https://github.com/IKIM-Essen/uncovar](https://github.com/IKIM-Essen/uncovar)

## How to execute the workflow?

Once you have
[installed mamba](https://mamba.readthedocs.io/en/latest/installation/micromamba-installation.html),
just follow the instructions
[here](https://snakemake.github.io/snakemake-workflow-catalog?usage=IKIM-Essen/uncovar).
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# Welcome to the Documentation of UnCoVar
# UnCoVar -- an open, extensible framework for virus genome analysis

<picture>
<source media="(prefers-color-scheme: dark)" srcset="https://github.com/IKIM-Essen/uncovar/assets/77535027/8e17c6fc-ff7a-4c25-afc9-7888036d693e">
<source media="(prefers-color-scheme: light)" srcset="https://github.com/IKIM-Essen/uncovar/assets/77535027/c99f5a94-749b-422e-b319-1e3700d40a8e">
<img alt="UnCoVar Logo dark/light">
</picture>

[![Snakemake](https://img.shields.io/badge/snakemake-≥6.3.0-brightgreen.svg)](https://snakemake.bitbucket.io)
[![GitHub actions status](https://github.com/koesterlab/snakemake-workflow-sars-cov2/workflows/Tests/badge.svg?branch=master)](https://github.com/koesterlab/snakemake-workflow-sars-cov2/actions?query=branch%3Amaster+workflow%3ATests)
[![Docker Repository on Quay](https://quay.io/repository/uncovar/uncovar/status "Docker Repository on Quay")](https://quay.io/repository/uncovar/uncovar)

UnCoVar is a reproducible and scalable workflow for transparent and robust
SARS-CoV-2 variant calling and lineage assignment with comprehensive reporting.
A Reproducible and Scalable Workflow for Transparent and Robust Virus Variant Calling and Lineage Assignment using SARS-CoV-2 as an example.

- Using state of the art tools, easily extended for other viruses

![UnCoVar tools](./assets/tools.png)

- Tools and database updates for critical components via Conda

- Built using modern design patterns with Conda and SnakeMake

- Extensible and easy to customize

<div class="row">
<div class="column">
<div class="card">
<div class="card-title">
<h3>Latest SARS-CoV-2 Lineage Assignment</h3>
</div>
<p>
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Proin molestie
neque scelerisque, bibendum nulla eget.
</p>
</div>
</div>
<div class="column">
<div class="card">
<div class="card-title">
<h3>Comprehensive Reporting</h3>
</div>
<p>
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Proin molestie
neque scelerisque, bibendum nulla eget.
</p>
</div>
</div>
</div>
- Customizable reporting with comprehensive visualization

<div class="row">
<div class="column">
<div class="card">
<div class="card-title">
<h3>Submission Ready Genomes</h3>
</div>
<p>
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Proin molestie
neque scelerisque, bibendum nulla eget.
</p>
</div>
</div>
<div class="column">
<div class="card">
<div class="card-title">
<h3>Easy to Customize</h3>
</div>
<p>
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Proin molestie
neque scelerisque, bibendum nulla eget.
</p>
</div>
</div>
</div>
![UnCoVar visuals](./assets/uncovar-displays.png)

[Getting Started](getting-started/){ .md-button }
[User Guide](user-guide/){ .md-button }
- Submission Ready Genomes

[introductory tutorial]: getting-started.md
[User Guide]: user-guide/index.md
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# Installation

## Installing

## Maintenance

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nav:
- Welcome: index.md
- Getting Started: getting-started.md
- Consumer Guide:
- Overview: consumer-guide/index.md
- Highlights: consumer-guide/first-impression.md
- Understanding the Report: consumer-guide/report-structure.md
- Lineages and Variants: consumer-guide/lineages-and-variants.md
- Submission Read Genomes: consumer-guide/submission-ready-genomes.md
- FAQs: consumer-guide/faqs.md
- User Guide:
- Overview: user-guide/index.md
- Installation: user-guide/installation.md
- Configuration: user-guide/configuration.md
- Create Your Analysis: user-guide/create-your-analysis.md
- Share Your Results: user-guide/share-your-results.md
- Customize Your Analysis: user-guide/customize-your-analysis.md
- FAQs: user-guide/faqs.md
- Developer Guide:
- Overview: dev-guide/index.md
- How to Contribute: dev-guide/contributing.md
- Pre-Analysis: dev-guide/pre-analysis.md
- Initial Quality Control: dev-guide/final-quality-control.md
- Sequence Preprocessing: dev-guide/sequence-preprocessing.md
- Assembly: dev-guide/assembly.md
- Lineage Calling: dev-guide/lineage-calling.md
- Variant Calling: dev-guide/variant-calling.md
- Reporting: dev-guide/reporting.md
- Final Quality Control: dev-guide/initial-quality-control.md
- Tests: dev-guide/tests.md
- CI/CD: dev-guide/ci-cd.md
- FAQs: dev-guide/faqs.md
- About:
- Team: about/team.md
- License: about/license.md
- Release Notes: about/changelog.md
- Benchmarking: benchmarking.md
- Installation: installation.md
- User Guide: user-guide.md
- Configuration: configuration.md
- FAQs: faq.md
- About: about.md

theme:
name: material
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