Ngs Collection

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🔮Psychic

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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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🔥Fire

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“An ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)”

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⚡Thunder

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“Official code repository for GATK versions 4 and up”

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🔮Psychic

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“Data intensive science for everyone.”

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⚔️Fighting

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“C library for high-throughput sequencing data formats”

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📦Normal

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“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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🔮Psychic

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“Tools to process and analyze deep sequencing data.”

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⚡Thunder

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“Java utilities for Bioinformatics”

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📦Normal

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“A collection of awesome things regarding all omics.”

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💻Normal

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“A One-Click System for Analyzing Loop-Resolution Hi-C Experiments”

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🔮Psychic

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“Customizable workflows based on snakemake and python for the analysis of NGS data”

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🔮Psychic

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“Bioconvert is a collaborative project to facilitate the interconversion of life science data from one format to another.”

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🔥Fire

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“Tools for working with genomic and high throughput sequencing data.”

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🔥Flame

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“A collection of Galaxy-related training material”

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⚡Thunder

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“A Java API for high-throughput sequencing data (HTS) formats.”

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📦Normal

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“Annotation and Ranking of Structural Variation”

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🔥Fire

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“SortMeRNA: next-generation sequence filtering and alignment tool”

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🔥Fire

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“UGENE is free open-source cross-platform bioinformatics software”