#计算机科学#DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Official code repository for GATK versions 4 and up
Data intensive science for everyone.
C library for high-throughput sequencing data formats
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, ...
Tools to process and analyze deep sequencing data.
A collection of awesome things regarding all omics.
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Customizable workflows based on snakemake and python for the analysis of NGS data
Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.
A collection of Galaxy-related training material
Tools for working with genomic and high throughput sequencing data.
SortMeRNA: next-generation sequence filtering and alignment tool
UGENE is free open-source cross-platform bioinformatics software
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data