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Awesome List
A curated list of awesome Bioinformatics libraries and software.
GitHub stars and default-branch commits for danielecook/Awesome-Bioinformatics.
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DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Pysam is a Python package for reading, manipulating, and writing genomics data such as SAM/BAM/CRAM and VCF/BCF files. It's a lightweight wrapper of the HTSlib API, the same one that powers samtools, bcftools, and tabix.
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
:rocket: seqfu - Sequece Fastx Utilities
A pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies
This is the SeqWare Project's main repo.
Pathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform