The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
-
Updated
Jun 3, 2025 - Python
The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
Small GATK alignment and variant calling pipeline using python
The second part of https://github.com/npanuhin/BIOCAD
A Snakemake pipeline for copy number variant calling without normal tissue samples
Germline variant calling pipeline
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.
Parse pileup files, generate consensus fasta and calculate heteroplasmy per nucleotide
💧 Automate message sending with Ngl, delivering one message per second for efficient communication and education purposes.
Scalable and High Performance Variant Calling on Cluster Environments
Map and post-process your bams for SNP calling
The DKFZ alignment workflow plugin originally developed at the eilslabs
Add a description, image, and links to the bwa topic page so that developers can more easily learn about it.
To associate your repository with the bwa topic, visit your repo's landing page and select "manage topics."