poreCovSARS-CoV-2 workflow for nanopore sequence data
scarfToolkit for highly memory efficient analysis of single-cell RNA-Seq, scATAC-Seq and CITE-Seq data. Analyze atlas scale datasets with millions of cells on laptop.
contact mapContact map analysis for biomolecules; based on MDTraj
sshashA compressed, associative, exact, and weighted dictionary for k-mers.
ginkgoCloud-based single-cell copy-number variation analysis tool
GLUEGraph-linked unified embedding for single-cell multi-omics data integration
SplitThreaderExplore rearrangements and copy-number amplifications in a cancer genome
chise.jsA web application to visualize and edit the pathway models represented by SBGN Process Description Notation
sdustSymmetric DUST for finding low-complexity regions in DNA sequences
dockstoreOur VM/Docker sharing infrastructure and management component
homerkitRead HOMER motif analysis output in R.
ngs-preprocessA pipeline for preprocessing NGS data from Illumina, Nanopore and PacBio technologies
haslrA fast tool for hybrid genome assembly of long and short reads
biocommons.seqreponon-redundant, compressed, journalled, file-based storage for biological sequences
atacrAnalysing Capture Seq Count Data
BioBlender21Blender plugin to process biological data and molecular work.
muscleMultiple sequence alignment with top benchmark scores scalable to thousands of sequences. Generates replicate alignments, enabling assessment of downstream analyses such as trees and predicted structures.
psammCuration and analysis of metabolic models
mokapotFast and flexible semi-supervised learning for peptide detection in Python
IMGTHLAGithub for files currently published in the IPD-IMGT/HLA FTP Directory hosted at the European Bioinformatics Institute
ontobiopython library for working with ontologies and ontology associations
orchidA novel management, annotation, and machine learning framework for analyzing cancer mutations
cromshellCLI for interacting with Cromwell servers
sintoTools for single-cell data processing
bionode-ncbiNode.js module for working with the NCBI API (aka e-utils).
SigProfilerSimulatorSigProfilerSimulator allows realistic simulations of mutational patterns and mutational signatures in cancer genomes. The tool can be used to simulate signatures of single point mutations, double point mutations, and insertion/deletions. Further, the tool makes use of SigProfilerMatrixGenerator and SigProfilerPlotting.
GenAMapVisual Machine Learning of Genome-Phenome Associations
DISCOVERDISCOVER co-occurrence and mutual exclusivity analysis for cancer genomics data
nthashntHash implementation in Rust
spacepharerSpacePHARER CRISPR Spacer Phage-Host pAiRs findER
dolphinnextA graphical user interface for distributed data processing of high throughput genomics
rust-lapperRust implementation of a fast, easy, interval tree library nim-lapper
arvA fast 23andMe DNA parser and inferrer for Python
nightingaleData visualisation web components for the life sciences.
HIBAGR package – HLA Genotype Imputation with Attribute Bagging (development version only)
CuteVCFsimple viewer for variant call format using htslib
vrs-pythonGA4GH Variation Representation Python Implementation
charcoalRemove contaminated contigs from genomes using k-mers and taxonomies.
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