irinastl's Stars
jupyter/jupyter
Jupyter metapackage for installation, docs and chat
MultiQC/MultiQC
Aggregate results from bioinformatics analyses across many samples into a single report.
samtools/hts-specs
Specifications of SAM/BAM and related high-throughput sequencing file formats
igvteam/igv.js
Embeddable genomic visualization component based on the Integrative Genomics Viewer
Illumina/hap.py
Haplotype VCF comparison tools
Illumina/SpliceAI
A deep learning-based tool to identify splice variants
ncbi/datasets
NCBI Datasets is a new resource that lets you easily gather data from across NCBI databases.
TransDecoder/TransDecoder
TransDecoder source
ga4gh/benchmarking-tools
Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls
PASApipeline/PASApipeline
PASA software
biopython/biopython.github.io
Source of biopython.org website, migrated from MediaWiki
mhahsler/rBLAST
Interface for the Basic Local Alignment Search Tool (BLAST) - R-Package
MikkelSchubert/adapterremoval
AdapterRemoval v2 - rapid adapter trimming, identification, and read merging
ga4gh/vrs
Extensible specification for representing and uniquely identifying biological sequence variation
CDCgov/phoenix
🔥🐦🔥PHoeNIx: A short-read pipeline for healthcare-associated and antimicrobial resistant pathogens
monarch-initiative/SEPIO-ontology
Ontology for representing scientific evidence and provenance information
klebgenomics/Kaptive
theiagen/public_health_bioinformatics
Bioinformatics workflows for genomic characterization, submission preparation, and genomic epidemiology of pathogens of public health concern.
samtools/htscodecs
Custom compression for CRAM and others.
ClinGen/clincoded
This GCI/VCI 1.0 platform has now been retired, and replaced with our new 2.0 platform:
UPHL-BioNGS/Grandeur
UPHL's Reference Free Pipeline
ImperialCardioGenetics/frequencyFilter
Allele frequency filtering for Mendelian variant discovery
BryantD/microtrace
Microblogging bot for tracery grammars.
marcoralab/MRcovid
ijmiller2/COVID-19_Multi-Omics
A repository for collaborative multi-omics data analysis & the covid-omics.app
covid19-hg/README
COVID-19 Host Genetics Initiative - analysis readme
ClinGen/gene-and-variant-curation-tools
ClinGen's gene and variant curation interfaces (GCI & VCI). Developed by Stanford ClinGen team.
CIBERER/Scourge-COVID19
marcoralab/multivariate_MR
mjpirinen/covid19-hgi_subtypes