bacnetBACNET is a Java based platform to develop website for multi-omics analysis
Stars: ✭ 12 (-92.77%)
GenevalidatorGeneValidator: Identify problems with predicted genes
Stars: ✭ 34 (-79.52%)
RNAseq titration resultsCross-platform normalization enables machine learning model training on microarray and RNA-seq data simultaneously
Stars: ✭ 22 (-86.75%)
Krakenuniq🐙 KrakenUniq: Metagenomics classifier with unique k-mer counting for more specific results
Stars: ✭ 123 (-25.9%)
FastqtFastQC port to Qt5: A quality control tool for high throughput sequence data.
Stars: ✭ 92 (-44.58%)
BwaBurrow-Wheeler Aligner for short-read alignment (see minimap2 for long-read alignment)
Stars: ✭ 970 (+484.34%)
DNAscanDNAscan is a fast and efficient bioinformatics pipeline that allows for the analysis of DNA Next Generation sequencing data, requiring very little computational effort and memory usage.
Stars: ✭ 36 (-78.31%)
genomediscoSoftware for comparing contact maps from HiC, CaptureC and other 3D genome data.
Stars: ✭ 23 (-86.14%)
tiptoftPredict plasmids from uncorrected long read data
Stars: ✭ 27 (-83.73%)
virnetVirNet: A deep attention model for viral reads identification
Stars: ✭ 26 (-84.34%)
ScgenSingle cell perturbation prediction
Stars: ✭ 122 (-26.51%)
picardmetrics🚦 Run Picard on BAM files and collate 90 metrics into one file.
Stars: ✭ 38 (-77.11%)
VdjvizA lightweight immune repertoire browser
Stars: ✭ 21 (-87.35%)
SigProfilerExtractorSigProfilerExtractor allows de novo extraction of mutational signatures from data generated in a matrix format. The tool identifies the number of operative mutational signatures, their activities in each sample, and the probability for each signature to cause a specific mutation type in a cancer sample. The tool makes use of SigProfilerMatrixGen…
Stars: ✭ 86 (-48.19%)
MolgenisMOLGENIS - for scientific data: management, exploration, integration and analysis.
Stars: ✭ 88 (-46.99%)
AMIDDIntroduction to Applied Mathematics and Informatics in Drug Discovery (AMIDD)
Stars: ✭ 13 (-92.17%)
polyRADGenotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
Stars: ✭ 16 (-90.36%)
ArtemisArtemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation
Stars: ✭ 135 (-18.67%)
bistroA library to build and execute typed scientific workflows
Stars: ✭ 43 (-74.1%)
NgsfEstimation of per-individual inbreeding coefficients under a probabilistic framework
Stars: ✭ 10 (-93.98%)
motifmatchrFast motif matching in R
Stars: ✭ 25 (-84.94%)
Awesome BioinformaticsA curated list of awesome Bioinformatics libraries and software.
Stars: ✭ 1,266 (+662.65%)
pathway-mapperPathwayMapper: An interactive and collaborative graphical curation tool for cancer pathways
Stars: ✭ 47 (-71.69%)
ScispacyA full spaCy pipeline and models for scientific/biomedical documents.
Stars: ✭ 855 (+415.06%)
awesome-geneticsA curated list of awesome bioinformatics software.
Stars: ✭ 60 (-63.86%)
BlacklistApplication for making ENCODE Blacklists
Stars: ✭ 119 (-28.31%)
block-alignerSIMD-accelerated library for computing global and X-drop affine gap penalty sequence-to-sequence or sequence-to-profile alignments using an adaptive block-based algorithm.
Stars: ✭ 58 (-65.06%)
NonpareilEstimate metagenomic coverage and sequence diversity
Stars: ✭ 26 (-84.34%)
crazydocRead DNA sequences from colourful Microsoft Word documents
Stars: ✭ 18 (-89.16%)
VdjtoolsPost-analysis of immune repertoire sequencing data
Stars: ✭ 85 (-48.8%)
chromapFast alignment and preprocessing of chromatin profiles
Stars: ✭ 93 (-43.98%)
PretzelJavascript full-stack framework for Big Data visualisation and analysis
Stars: ✭ 26 (-84.34%)
Metasra PipelineMetaSRA: normalized sample-specific metadata for the Sequence Read Archive
Stars: ✭ 33 (-80.12%)
Soapdenovo2Next generation sequencing reads de novo assembler.
Stars: ✭ 150 (-9.64%)
BioKEENA computational library for learning and evaluating biological knowledge graph embeddings
Stars: ✭ 41 (-75.3%)
Metacachememory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Stars: ✭ 26 (-84.34%)
ccsCCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
Stars: ✭ 79 (-52.41%)
GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
Stars: ✭ 64 (-61.45%)
PyensemblrestA wrapper for the EnsEMBL REST API
Stars: ✭ 25 (-84.94%)
bio toolsUseful bioinformatic scripts
Stars: ✭ 35 (-78.92%)
Dna2vecdna2vec: Consistent vector representations of variable-length k-mers
Stars: ✭ 117 (-29.52%)
ngstoolsMy own tools code for NGS data analysis (Next Generation Sequencing)
Stars: ✭ 28 (-83.13%)
RiddleRace and ethnicity Imputation from Disease history with Deep LEarning
Stars: ✭ 91 (-45.18%)
conda-env-builderBuild and maintain multiple custom conda environments all in once place.
Stars: ✭ 18 (-89.16%)
PCG𝙋𝙝𝙮𝙡𝙤𝙜𝙚𝙣𝙚𝙩𝙞𝙘 𝘾𝙤𝙢𝙥𝙤𝙣𝙚𝙣𝙩 𝙂𝙧𝙖𝙥𝙝 ⸺ Haskell program and libraries for general phylogenetic graph search
Stars: ✭ 20 (-87.95%)
EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
Stars: ✭ 25 (-84.94%)
ProtrComprehensive toolkit for generating various numerical features of protein sequences
Stars: ✭ 30 (-81.93%)
SemiBinNo description or website provided.
Stars: ✭ 25 (-84.94%)
dna-traitsA fast 23andMe genome text file parser, now superseded by arv
Stars: ✭ 64 (-61.45%)
Awesome Single CellCommunity-curated list of software packages and data resources for single-cell, including RNA-seq, ATAC-seq, etc.
Stars: ✭ 1,937 (+1066.87%)
BiosyntaxSyntax highlighting for computational biology
Stars: ✭ 164 (-1.2%)
RagooFast Reference-Guided Scaffolding of Genome Assembly Contigs. RagTag, the successor to RaGOO, is now available here: https://github.com/malonge/RagTag
Stars: ✭ 158 (-4.82%)