gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
Stars: ✭ 27 (+0%)
plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
Stars: ✭ 27 (+0%)
saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
Stars: ✭ 17 (-37.04%)
mlst checkMultilocus sequence typing by blast using the schemes from PubMLST
Stars: ✭ 22 (-18.52%)
assembly improvementImprove the quality of a denovo assembly by scaffolding and gap filling
Stars: ✭ 46 (+70.37%)
snp-sitesFinds SNP sites from a multi-FASTA alignment file
Stars: ✭ 182 (+574.07%)
gubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 103 (+281.48%)
haslrA fast tool for hybrid genome assembly of long and short reads
Stars: ✭ 68 (+151.85%)
AribaAntimicrobial Resistance Identification By Assembly
Stars: ✭ 96 (+255.56%)
GubbinsRapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Stars: ✭ 67 (+148.15%)
pepperPEPPER-Margin-DeepVariant
Stars: ✭ 179 (+562.96%)
Clair3Clair3 - Symphonizing pileup and full-alignment for high-performance long-read variant calling
Stars: ✭ 119 (+340.74%)
rkmhClassify sequencing reads using MinHash.
Stars: ✭ 42 (+55.56%)
streamformaticsReal-time species-typing visualisation for nanopore data.
Stars: ✭ 13 (-51.85%)
CirclatorA tool to circularize genome assemblies
Stars: ✭ 121 (+348.15%)
RoaryRapid large-scale prokaryote pan genome analysis
Stars: ✭ 176 (+551.85%)
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 (+400%)
bystroBystro genetic analysis (annotation, filtering, statistics)
Stars: ✭ 31 (+14.81%)
BiopythonOfficial git repository for Biopython (originally converted from CVS)
Stars: ✭ 2,936 (+10774.07%)
CanvasxpressJavaScript VisualizationTools
Stars: ✭ 247 (+814.81%)
netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
Stars: ✭ 23 (-14.81%)
LRSDAYLRSDAY: Long-read Sequencing Data Analysis for Yeasts
Stars: ✭ 26 (-3.7%)
Bedops🔬 BEDOPS: high-performance genomic feature operations
Stars: ✭ 215 (+696.3%)
MGSEMapping-based Genome Size Estimation (MGSE) performs an estimation of a genome size based on a read mapping to an existing genome sequence assembly.
Stars: ✭ 22 (-18.52%)
chromapFast alignment and preprocessing of chromatin profiles
Stars: ✭ 93 (+244.44%)
reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
Stars: ✭ 64 (+137.04%)
Cyvcf2cython + htslib == fast VCF and BCF processing
Stars: ✭ 243 (+800%)
BowtieAn ultrafast memory-efficient short read aligner
Stars: ✭ 221 (+718.52%)
Hap.pyHaplotype VCF comparison tools
Stars: ✭ 249 (+822.22%)
MiniasmUltrafast de novo assembly for long noisy reads (though having no consensus step)
Stars: ✭ 216 (+700%)
STingUltrafast sequence typing and gene detection from NGS raw reads
Stars: ✭ 15 (-44.44%)
wenganAn accurate and ultra-fast hybrid genome assembler
Stars: ✭ 81 (+200%)
TALONTechnology agnostic long read analysis pipeline for transcriptomes
Stars: ✭ 96 (+255.56%)
WinnowmapLong read / genome alignment software
Stars: ✭ 151 (+459.26%)
swan visA Python library to visualize and analyze long-read transcriptomes
Stars: ✭ 35 (+29.63%)
dentistClose assembly gaps using long-reads at high accuracy.
Stars: ✭ 39 (+44.44%)
interARTICInterARTIC - An interactive local web application for viral whole genome sequencing utilising the artic network pipelines..
Stars: ✭ 22 (-18.52%)
TOGATOGA (Tool to infer Orthologs from Genome Alignments): implements a novel paradigm to infer orthologous genes. TOGA integrates gene annotation, inferring orthologs and classifying genes as intact or lost.
Stars: ✭ 35 (+29.63%)
RATTLEReference-free reconstruction and error correction of transcriptomes from Nanopore long-read sequencing
Stars: ✭ 35 (+29.63%)
IsoQuantReference-based transcript discovery from long RNA read
Stars: ✭ 26 (-3.7%)
MinigraphProof-of-concept seq-to-graph mapper and graph generator
Stars: ✭ 206 (+662.96%)
Scaff10XPipeline for scaffolding and breaking a genome assembly using 10x genomics linked-reads
Stars: ✭ 21 (-22.22%)
PHATPathogen-Host Analysis Tool - A modern Next-Generation Sequencing (NGS) analysis platform
Stars: ✭ 17 (-37.04%)
ccsCCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
Stars: ✭ 79 (+192.59%)
faster lmm dA faster lmm for GWAS. Supports GPU backend.
Stars: ✭ 12 (-55.56%)
wgs2ncbiToolkit for preparing genomes for submission to NCBI
Stars: ✭ 25 (-7.41%)
GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
Stars: ✭ 64 (+137.04%)
dysgudysgu-SV is a collection of tools for calling structural variants using short or long reads
Stars: ✭ 47 (+74.07%)
fast-sgFast-SG: An alignment-free algorithm for ultrafast scaffolding graph construction from short or long reads.
Stars: ✭ 22 (-18.52%)
wdlRunRElastic, reproducible, and reusable genomic data science tools from R backed by cloud resources
Stars: ✭ 34 (+25.93%)
jgi-queryA simple command-line tool to download data from Joint Genome Institute databases
Stars: ✭ 38 (+40.74%)
unimapA EXPERIMENTAL fork of minimap2 optimized for assembly-to-reference alignment
Stars: ✭ 76 (+181.48%)
pyrpipeReproducible bioinformatics pipelines in python. Import any Unix tool/command in python.
Stars: ✭ 53 (+96.3%)
simplesamSimple pure Python SAM parser and objects for working with SAM records
Stars: ✭ 50 (+85.19%)
catchA package for designing compact and comprehensive capture probe sets.
Stars: ✭ 55 (+103.7%)
nPhasePloidy agnostic phasing pipeline and algorithm
Stars: ✭ 18 (-33.33%)
calN50Compute N50/NG50 and auN/auNG
Stars: ✭ 20 (-25.93%)
companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
Stars: ✭ 21 (-22.22%)