lightdockProtein-protein, protein-peptide and protein-DNA docking framework based on the GSO algorithm
Stars: ✭ 110 (+633.33%)
gblastnG-BLASTN is a GPU-accelerated nucleotide alignment tool based on the widely used NCBI-BLAST.
Stars: ✭ 52 (+246.67%)
Repo-BioBinomica Public Repository for Biological Parts
Stars: ✭ 21 (+40%)
adaptA package for designing activity-informed nucleic acid diagnostics for viruses.
Stars: ✭ 16 (+6.67%)
snpstools for reading, writing, merging, and remapping SNPs
Stars: ✭ 57 (+280%)
variantkeyNumerical Encoding for Human Genetic Variants
Stars: ✭ 32 (+113.33%)
pydnaClone with Python! Data structures for double stranded DNA & simulation of homologous recombination, Gibson assembly, cut & paste cloning.
Stars: ✭ 109 (+626.67%)
polyply 1.0Generate input parameters and coordinates for atomistic and coarse-grained simulations of polymers, ssDNA, and carbohydrates
Stars: ✭ 59 (+293.33%)
STingUltrafast sequence typing and gene detection from NGS raw reads
Stars: ✭ 15 (+0%)
arvA fast 23andMe DNA parser and inferrer for Python
Stars: ✭ 98 (+553.33%)
bamgineerBamgineer: Introduction of simulated allele-specific copy number variants into exome and targeted sequence data sets
Stars: ✭ 35 (+133.33%)
sequenceworkprograms and scripts, mainly python, for analyses related to nucleic or protein sequences
Stars: ✭ 22 (+46.67%)
coalaA Framework for Coalescent Simulation in R
Stars: ✭ 21 (+40%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+19473.33%)
HtsjdkA Java API for high-throughput sequencing data (HTS) formats.
Stars: ✭ 220 (+1366.67%)
DeepvariantDeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Stars: ✭ 2,404 (+15926.67%)
ShastaDe novo assembly from Oxford Nanopore reads.
Stars: ✭ 188 (+1153.33%)
Pyrosetta.notebooksJupyter Notebooks for learning the PyRosetta platform for biomolecular structure prediction and design
Stars: ✭ 116 (+673.33%)
UgeneUGENE is free open-source cross-platform bioinformatics software
Stars: ✭ 112 (+646.67%)
GenomicsA collection of scripts and notes related to genomics and bioinformatics
Stars: ✭ 101 (+573.33%)
Abra2ABRA2
Stars: ✭ 65 (+333.33%)
SnsAnalysis pipelines for sequencing data
Stars: ✭ 43 (+186.67%)
GatkOfficial code repository for GATK versions 4 and up
Stars: ✭ 1,002 (+6580%)
Flu PredictionPredicting Future Influenza Virus Sequences with Machine Learning
Stars: ✭ 20 (+33.33%)
Restez😴 📂 Create and Query a Local Copy of GenBank in R
Stars: ✭ 22 (+46.67%)
GalaxyData intensive science for everyone.
Stars: ✭ 812 (+5313.33%)
Vgtools for working with genome variation graphs
Stars: ✭ 710 (+4633.33%)
NucleusPython and C++ code for reading and writing genomics data.
Stars: ✭ 657 (+4280%)
KhmerIn-memory nucleotide sequence k-mer counting, filtering, graph traversal and more
Stars: ✭ 640 (+4166.67%)
Dna 3d Engine3d engine implementation in DNA code!
Stars: ✭ 493 (+3186.67%)
Icewater16,432 Free Yara rules created by
Stars: ✭ 324 (+2060%)
PyfaidxEfficient pythonic random access to fasta subsequences
Stars: ✭ 307 (+1946.67%)
Bio.jl[DEPRECATED] Bioinformatics and Computational Biology Infrastructure for Julia
Stars: ✭ 257 (+1613.33%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (+326.67%)
TKViewerNexusTK DAT Object Viewer
Stars: ✭ 18 (+20%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (+300%)
seqvizDNA sequence viewer supporting custom, GenBank, FASTA, NCBI accession, and iGEM input.
Stars: ✭ 99 (+560%)
orfipyFast and flexible ORF finder
Stars: ✭ 27 (+80%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (+266.67%)
benchling-apiA python wrapper for the benchling api
Stars: ✭ 39 (+160%)
nafNucleotide Archival Format - Compressed file format for DNA/RNA/protein sequences
Stars: ✭ 35 (+133.33%)
cobsCOBS - Compact Bit-Sliced Signature Index (for Genomic k-Mer Data or q-Grams)
Stars: ✭ 64 (+326.67%)
hlatypingPrecision HLA typing from next-generation sequencing data
Stars: ✭ 28 (+86.67%)
PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
Stars: ✭ 17 (+13.33%)
seqfoldminimalistic nucleic acid folding
Stars: ✭ 39 (+160%)
polyA Go package for engineering organisms.
Stars: ✭ 270 (+1700%)
BuddySuiteBioinformatics toolkits for manipulating sequence, alignment, and phylogenetic tree files
Stars: ✭ 106 (+606.67%)
FluentDNAFluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
Stars: ✭ 52 (+246.67%)