DeeptoolsTools to process and analyze deep sequencing data.
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Mutual labels: bioinformatics, genomics, ngs
catchA package for designing compact and comprehensive capture probe sets.
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Mutual labels: bioinformatics, genomics, ngs
JvarkitJava utilities for Bioinformatics
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Mutual labels: bioinformatics, genomics, ngs
GalaxyData intensive science for everyone.
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Mutual labels: bioinformatics, genomics, ngs
GatkOfficial code repository for GATK versions 4 and up
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Mutual labels: bioinformatics, genomics, ngs
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+3656.25%)
Mutual labels: bioinformatics, genomics, ngs
NglessNGLess: NGS with less work
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Mutual labels: bioinformatics, genomics, ngs
GGR-cwlCWL tools and workflows for GGR
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Mutual labels: dnase-seq, chip-seq, atac-seq
MTBseq sourceMTBseq is an automated pipeline for mapping, variant calling and detection of resistance mediating and phylogenetic variants from illumina whole genome sequence data of Mycobacterium tuberculosis complex isolates.
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Mutual labels: genomics, ngs
ntHashFast hash function for DNA sequences
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Mutual labels: bioinformatics, genomics
atroposAn NGS read trimming tool that is specific, sensitive, and speedy. (production)
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Mutual labels: bioinformatics, ngs
simplesamSimple pure Python SAM parser and objects for working with SAM records
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Mutual labels: bioinformatics, genomics
wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
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Mutual labels: bioinformatics, genomics
saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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Mutual labels: bioinformatics, genomics
dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
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Mutual labels: bioinformatics, genomics
unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
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Mutual labels: bioinformatics, genomics
CENTIPEDE.tutorial🐛 How to use CENTIPEDE to determine if a transcription factor is bound.
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Mutual labels: bioinformatics, dnase-seq
bystroBystro genetic analysis (annotation, filtering, statistics)
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Mutual labels: bioinformatics, genomics
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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Mutual labels: bioinformatics, genomics