The second part of https://github.com/npanuhin/BIOCAD
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Updated
Mar 12, 2021 - Python
The second part of https://github.com/npanuhin/BIOCAD
The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
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Complete pipeline that mirrors the manuscript: reference based assembly with depth masking, de novo checks, phylogeny with configurable models including ModelFinder, and targeted mutation analysis for G and F versus NC_038235.1 and NC_001781.1. Includes CI and environment files for easy setup.
Germline variant calling pipeline
A Snakemake pipeline for copy number variant calling without normal tissue samples
Parse pileup files, generate consensus fasta and calculate heteroplasmy per nucleotide
Small GATK alignment and variant calling pipeline using python
Map and post-process your bams for SNP calling
The DKFZ alignment workflow plugin originally developed at the eilslabs
Scalable and High Performance Variant Calling on Cluster Environments
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