py-mappy (V) | | Minimap2 python binding |
py-mdanalysis (V) | | Library to analyze and manipulate molecular dynamics trajectories |
py-mdtraj (V) | | The analysis of molecular dynamics trajectories |
py-mmLib (V) | | Python Macromolecular Library |
py-multiqc | | Aggregate bioinformatics analysis reports across samples and tools |
py-neo (V) | | Python package for representing electrophysiology data |
py-nibabel (V) | | Access a multitude of neuroimaging data formats |
py-nilearn (V) | | Statistical learning for neuroimaging in Python |
py-prody (V) | | Python Package for Protein Dynamics Analysis |
py-psychopy (V) | | Psychology and neuroscience software in python |
py-pydicom | | Pure python package for working with DICOM files |
py-pygr (V) | | Pygr graph database for bioinformatics |
py-pyquante (V) | | Quantum chemistry in Python |
py-pysam (V) | | Python module for reading, manipulating and writing genomic data sets |
py-pysb (V) | | Python Systems Biology modeling framework |
py-spglib (V) | | Python bindings for finding and handling crystal symmetries |
py-sumatra (V) | | Tracking projects based on numerical simulation or analysis |
py-thermo (V) | | Chemical properties component of ChEDL |
py-thermopy (V) | | Some utilities for Thermodynamics and Thermochemistry |
py-varify (V) | | Clinical DNA Sequencing Analysis and Data Discovery |
R-popbio | | Construction and Analysis of Matrix Population Models |
R-rgbif (V) | | Interface to the Global Biodiversity Information Facility API |
racon | | Genomic consensus builder |
rasmol | | Molecular Graphics Visualisation Tool |
readseq (V) | | Read and reformat biosequences, Java command-line version |
rna-seq | | Core tools needed for RNA-Seq analysis |
rna-star | | Spliced Transcripts Alignment to a Reference |
samtools | | Tools for manipulating sequence alignment maps |
seqtk | | Tool for processing sequences in FASTA/FASTQ format |
sewer | | SEquence Analysis using WEb Resources |
sra-tools | | NCBI's toolkit for handling data in INSDC Sequence Read Archives |
stacks | | Software pipeline for building loci from short-read sequences |
stride | | Protein secondary structure assignment from atomic coordinates |
stringtie | | Transcript assembly and quantification for RNA-seq |
trimmomatic | | Flexible read trimming tool for Illumina NGS data |
vcf-split | | Split a multi-sample VCF into single-sample VCFs |
vcf2hap | | Generate .hap file from VCF for haplohseq |
vsearch | | Versatile open-source tool for metagenomics |
xmakemol | | Program for visualizing atomic and molecular systems |
xylem | | Tools for manipulation of genetic databases |