PyensemblrestA wrapper for the EnsEMBL REST API
Stars: ✭ 25 (-69.51%)
Mmseqs2MMseqs2: ultra fast and sensitive search and clustering suite
Stars: ✭ 441 (+437.8%)
cloud-genomicsIntroduction to Cloud Computing for Genomics
Stars: ✭ 13 (-84.15%)
PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
Stars: ✭ 17 (-79.27%)
streamformaticsReal-time species-typing visualisation for nanopore data.
Stars: ✭ 13 (-84.15%)
TypeTEGenotyping of segregating mobile elements insertions
Stars: ✭ 15 (-81.71%)
Mygene.infoMyGene.info: A BioThings API for gene annotations
Stars: ✭ 79 (-3.66%)
StartappThe START App: R Shiny Transcriptome Analysis Resource Tool
Stars: ✭ 73 (-10.98%)
Qiime16stutorialA tutorial on methods of 16S analysis with QIIME 1
Stars: ✭ 59 (-28.05%)
Metasra PipelineMetaSRA: normalized sample-specific metadata for the Sequence Read Archive
Stars: ✭ 33 (-59.76%)
WdlWorkflow Description Language - Specification and Implementations
Stars: ✭ 438 (+434.15%)
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 (-29.27%)
GoenrichGO enrichment with python -- pandas meets networkx
Stars: ✭ 80 (-2.44%)
open-cravatA modular annotation tool for genomic variants
Stars: ✭ 74 (-9.76%)
viralrecallDetection of NCLDV signatures in 'omic data
Stars: ✭ 15 (-81.71%)
hts-pythonpythonic wrapper for htslib
Stars: ✭ 18 (-78.05%)
Elvers(formerly eelpond) an automated RNA-Seq workflow system
Stars: ✭ 22 (-73.17%)
souporcellClustering scRNAseq by genotypes
Stars: ✭ 88 (+7.32%)
jbrowse-componentsMonorepo with JBrowse 2 web, JBrowse 2 desktop, the JB core package, and core plugins. To customize behaviors, write an in-house plugin.
Stars: ✭ 89 (+8.54%)
get phylomarkersA pipeline to select optimal markers for microbial phylogenomics and species tree estimation using coalescent and concatenation approaches
Stars: ✭ 34 (-58.54%)
snakefmtThe uncompromising Snakemake code formatter
Stars: ✭ 78 (-4.88%)
koverLearn interpretable computational phenotyping models from k-merized genomic data
Stars: ✭ 47 (-42.68%)
JampJAMP - Just Another Metabarcoding Pipeline
Stars: ✭ 19 (-76.83%)
AssemblyticsAssemblytics is a bioinformatics tool to detect and analyze structural variants from a genome assembly by comparing it to a reference genome.
Stars: ✭ 105 (+28.05%)
BioDA D library for computational biology and bioinformatics
Stars: ✭ 45 (-45.12%)
gosling.jsGrammar of Scalable Linked Interactive Nucleotide Graphics
Stars: ✭ 89 (+8.54%)
Arcs🌈Scaffold genome sequence assemblies using linked read sequencing data
Stars: ✭ 67 (-18.29%)
bxtoolsTools for analyzing 10X Genomics data
Stars: ✭ 39 (-52.44%)
immunedbImmuneDB - A system for the analysis and exploration of high-throughput adaptive immune receptor sequencing data
Stars: ✭ 13 (-84.15%)
MindTheGapMindTheGap is a SV caller for short read sequencing data dedicated to insertion variants (all sizes and types). It can also be used as a local assembly tool.
Stars: ✭ 30 (-63.41%)
Nsga Iian implementation of NSGA-II in java
Stars: ✭ 18 (-78.05%)
docker-builds📦 🐳 Dockerfiles and documentation on tools for public health bioinformatics
Stars: ✭ 84 (+2.44%)
gnomixA fast, scalable, and accurate local ancestry method.
Stars: ✭ 36 (-56.1%)
VerifybamidVerifyBamID2: A robust tool for DNA contamination estimation from sequence reads using ancestry-agnostic method.
Stars: ✭ 44 (-46.34%)
tidygenomicsTidy Verbs for Dealing with Genomic Data Frames https://const-ae.github.io/tidygenomics/
Stars: ✭ 97 (+18.29%)
lexicon-mono-seqDOM Text Based Multiple Sequence Alignment Library
Stars: ✭ 15 (-81.71%)
TADLibA Library to Explore Chromatin Interaction Patterns for Topologically Associating Domains
Stars: ✭ 23 (-71.95%)
Splatter PaperData and analysis for the Splatter paper
Stars: ✭ 17 (-79.27%)
fqCommand line utility for manipulating Illumina-generated FastQ files.
Stars: ✭ 31 (-62.2%)
MMseqs2-AppMMseqs2 app to run on your workstation or servers
Stars: ✭ 16 (-80.49%)
OswitchProvides access to complex Bioinformatics software (even BioLinux!) in just one command.
Stars: ✭ 75 (-8.54%)
Circosjsd3 library to build circular graphs
Stars: ✭ 436 (+431.71%)
crazydocRead DNA sequences from colourful Microsoft Word documents
Stars: ✭ 18 (-78.05%)
mustacheMulti-scale Detection of Chromatin Loops from Hi-C and Micro-C Maps using Scale-Space Representation
Stars: ✭ 38 (-53.66%)
GCModellerGCModeller: genomics CAD(Computer Assistant Design) Modeller system in .NET language
Stars: ✭ 25 (-69.51%)
ManormA robust model for quantitative comparison of ChIP-Seq data sets.
Stars: ✭ 16 (-80.49%)
phastafIdentify phage regions in bacterial genomes for masking purposes
Stars: ✭ 22 (-73.17%)
FastpAn ultra-fast all-in-one FASTQ preprocessor (QC/adapters/trimming/filtering/splitting/merging...)
Stars: ✭ 966 (+1078.05%)
epivizEpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding of correlations between various genome features.
Stars: ✭ 65 (-20.73%)
spark-vcfSpark VCF data source implementation for Dataframes
Stars: ✭ 15 (-81.71%)
Jigvigv.js server and automatic configuration to view bam/cram/vcf/bed. "working in under 1 minute"
Stars: ✭ 43 (-47.56%)
ContainersBioinformatics containers
Stars: ✭ 435 (+430.49%)
perbasePer-base per-nucleotide depth analysis
Stars: ✭ 46 (-43.9%)
geneviewGenomics data visualization in Python by using matplotlib.
Stars: ✭ 38 (-53.66%)
ProtrComprehensive toolkit for generating various numerical features of protein sequences
Stars: ✭ 30 (-63.41%)
RushA cross-platform command-line tool for executing jobs in parallel
Stars: ✭ 421 (+413.41%)
BioKEENA computational library for learning and evaluating biological knowledge graph embeddings
Stars: ✭ 41 (-50%)
flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
Stars: ✭ 73 (-10.98%)