Lists (1)
Sort Name ascending (A-Z)
Starred repositories
Various algorithms for analysing genomics data
Microsoft PowerToys is a collection of utilities that help you customize Windows and streamline everyday tasks
andersen-lab / ivar
Forked from gkarthik/ivariVar is a computational package that contains functions broadly useful for viral amplicon-based sequencing.
Scalable and flexible workflow orchestration platform that seamlessly unifies data, ML and analytics stacks.
🔥🐦🔥PHoeNIx: a platform agnostic pipeline for healthcare-associated and antimicrobial resistant pathogens
Universal workbench incorporating msdial, msfinder, and mrmprobs
The Tripal package is a suite of Drupal modules for creating biological (genomic, genetic, breeding) websites. Visit the Tripal homepage at http://tripal.info for documentation, support, and other …
Official code repository for GATK versions 4 and up
Meteor is a plateform for quantitative metagenomics profiling of complex ecosystems. Meteor relies on genes catalogue to perform species-level taxonomic profiling (Bacteria, Archaea and Eukaryotes)…
180+ Java applications for analyzing next generation sequencing data from ChIPSeq, RNASeq, BisSeq, DNASeq, variant annotation/ filtering, alignment/VCF QC, capture array design, IGV/ DAS2/IGB/UCSC …
MGnify genome analysis pipeline
HemTools: a collection of NGS pipelines and bioinformatic analyses
Amplicon sequence processing workflow using QIIME 2 and Snakemake
web-based analysis tool for rare disease genomics
An open-source remote desktop application designed for self-hosting, as an alternative to TeamViewer.
A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
repository of the 3-day course "First steps with Python in Life Sciences" from SIB-training
Efficient retrieval, download, and unification of genomic data from leading biodiversity databases
Amplicon sequencing analysis workflow using DADA2 and QIIME2
A modular annotation tool for genomic variants
An analysis and visualization platform for 'omics data
Bacterial typing pipeline for clinical NGS data. Written in NextFlow, Python & Bash.
FROGS is a galaxy/CLI workflow designed to produce an OTUs count matrix from high depth sequencing amplicon data.
Short-read and long-read sequencing tools for diagnostics
Sequana: a set of Snakemake NGS pipelines
Whole exome sequencing pipeline for inherited diseases