A Snakemake pipeline for copy number variant calling without normal tissue samples
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Updated
Jun 19, 2024 - Python
A Snakemake pipeline for copy number variant calling without normal tissue samples
1,674 S.cerevisiae genomics data
Nextflow pipeline for BWA, BWA2 and STAR alignments
NGLess: NGS with less work
Genomic Analysis Pipeline: Automate data preprocessing, variant calling, and annotation with Snakemake. Ensure reproducibility and reliability in genomic studies.
The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
Whole Exome/Whole Genome Sequencing alignment pipeline
Bulk Rna-seq Analysis
The DKFZ alignment workflow plugin originally developed at the eilslabs
Detecting contamination in NGS data and multi-species analysis
Tech Stack: React, and Tailwind CSS
Create required reference genome index files for WGS data analysis
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