The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
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Updated
Apr 7, 2024 - Python
The snakyVC pipeline is designed for efficiently and parallelly executing variant calling on next-generation sequencing (NGS) whole-genome datasets.
A Snakemake pipeline for copy number variant calling without normal tissue samples
Bulk Rna-seq Analysis
Build Docker container for BWA and (optionally) convert to Apptainer/Singularity.
msgen: R functions for interfacing with the Microsoft Genomics service on Azure.
Parse pileup files, generate consensus fasta and calculate heteroplasmy per nucleotide
this is just impelementation from movie ticketing like cinema21, just simple and buat pusing. hahahah.
Genomic Analysis Pipeline: Automate data preprocessing, variant calling, and annotation with Snakemake. Ensure reproducibility and reliability in genomic studies.
BWA-based alignment of CRISPR gRNA spacer sequences
Small GATK alignment and variant calling pipeline using python
Scalable and High Performance Variant Calling on Cluster Environments
Highly optimized Burrow-Wheeler Aligner specifically for Illumina ~150 bp short-read alignment.
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