Astrometry.net Tycho-2 big endian index files (30'-44')
Astrometry.net Tycho-2 little endian index files (30'-44')
Astrometry.net Tycho-2 index files (44'-60')
Astrometry.net Tycho-2 big endian index files (44'-60')
Astrometry.net Tycho-2 little endian index files (44'-60')
Astrometry.net Tycho-2 index files (60'-2000')
Astrometry.net Tycho-2 big endian index files (60'-2000')
Astrometry.net Tycho-2 little endian index files (60'-2000')
Astrometry plate solver
astronomical almanac - calculate planet and star positions
Command line tools from astropy
Debian Astronomy Pure Blend (tasksel tasks)
genome assembly-to-assembly comparison
ATAC-seq QC and visualization
atomic-scale 3D modeling toolbox
atomic-scale 3D modeling toolbox (data)
NGS read trimming tool that is specific, sensitive, and speedy
pipeline components for real-time virus analysis
gene prediction in eukaryotic genomes
data files for AUGUSTUS
analysis of ligand binding to protein structure
instructions for getData to collect compounds
test files for AutoDock
docking of small molecules to proteins
pre-calculate binding of ligands to their receptor
test files for AutoGrid
Conversion of ESRI Arcinfo Vector Coverage in E00 format
Molecular Graphics and Modelling System
Molecular Graphics and Modelling System (library)
Trie-based DNA sequencing read demultiplexer
Computational Chemistry Package
software package for designing hybrid enrichment probes
Bayesian Inference of Alignment and Phylogeny
Remove gene-specific primer sequences from SAM/BAM alignments
tools for common BAM file manipulations
toolkit for manipulating BAM (genome alignment) files
Bioinformatics Application for Navigating De novo Assembly Graphs Easily
Bioinformatics Application for Navigating De novo Assembly Graphs Easily (data)
rapid ribosomal RNA prediction
tools for computational magnetic resonance imaging
viewer for multi-dimensional complex-valued data
BBTools genomic aligner and other tools for short sequences
short read aligner and other bioinformatic tools - JNI library
de Bruijn compaction in low memory
genomic variant calling and manipulation of VCF/BCF files
2-DE electrophoresis gel image spot detection
Genotype calling, genotype phasing and imputation of ungenotyped markers
Bayesian MCMC phylogenetic inference
high-performance genomic feature operations