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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.
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Mar 10, 2025 - Python
An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
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Nov 28, 2024 - C++
Official code repository for GATK versions 4 and up
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Mar 16, 2025 - Java
Data intensive science for everyone.
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Mar 16, 2025 - Python
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.
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Feb 13, 2025 - Cython
A collection of awesome things regarding all omics.
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Jan 23, 2024
Java utilities for Bioinformatics
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Mar 16, 2025 - Java
A One-Click System for Analyzing Loop-Resolution Hi-C Experiments
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Nov 22, 2024 - Shell
Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.
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Dec 1, 2023 - Python
A collection of Galaxy-related training material
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Mar 17, 2025 - HTML
Tools for working with genomic and high throughput sequencing data.
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Mar 13, 2025 - Scala
SortMeRNA: next-generation sequence filtering and alignment tool
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Jan 1, 2025 - C++
Annotation and Ranking of Structural Variation
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Mar 6, 2025 - Tcl
UGENE is free open-source cross-platform bioinformatics software
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Mar 13, 2025 - C++
A cool place to store your Hi-C
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Mar 10, 2025 - Python
Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data
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May 14, 2020 - Python
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