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Package Name Access Summary Updated
aliview public AliView is an intuitive and fast alignment viewer and editor for DNA and amino acid sequences. 2025-03-10
cleanifier public A fast lightweight tool to remove contamination using k-mers. 2025-03-10
severus public A tool for somatic structural variant calling using long reads 2025-03-10
hmftools-esvee public Structural variant caller specialised for breakend-breakpoint calling. 2025-03-10
hmftools-linx public LINX is an annotation, interpretation and visualisation tool for structural variants. 2025-03-10
hmftools-pave public PAVE annotates SNV/MNV/INDEL calls with consequence on corresponding genes, transcripts, and proteins. 2025-03-10
r-pathosurveilr public Utilities for interacting with the pathogensurveillance pipeline. 2025-03-10
grepq public Quickly filter FASTQ files. 2025-03-09
olivar public Olivar PCR tiling design 2025-03-09
captus public Captus: Assembly of Phylogenomic Datasets from High-Throughput Sequencing data 2025-03-09
artic public ARTIC pipeline - a bioinformatics pipeline for working with virus sequencing data sequenced with nanopore. 2025-03-09
pybwa public Pybwa is a python module that makes it easy to align sequence data. It is a lightweight wrapper of bwa. 2025-03-08
galaxy-data public The Galaxy models, datatype framework, and datatype implementations. 2025-03-08
galaxy-files public The Galaxy file sources framework and default plugins. 2025-03-08
galaxy-objectstore public The Galaxy object store framework and default implementations 2025-03-08
galaxy-schema public The Galaxy API schema objects. 2025-03-08
postmaster public Postmaster is a tool for annotating transcriptome alignments with posterior alignment probabilities derived from salmon quantifications. 2025-03-08
danbing-tk public Toolkit for VNTR genotyping and repeat-pan genome graph construction 2025-03-08
longbow public A Python program for nanopore sequencing basecalling configuration prediction 2025-03-08
miniprot public Miniprot aligns a protein sequence against a genome with affine gap penalty, splicing and frameshift. It is primarily intended for annotating protein-coding genes in a new species using known genes from other species. 2025-03-08
last public LAST finds & aligns related regions of sequences. 2025-03-07
gmap public Genomic mapping and alignment program for mRNA and EST sequences. 2025-03-07
callingcardstools public An API and collection of cmd line tools to work with calling cards sequencing data 2025-03-07
taxtastic public Tools for taxonomic naming and annotation 2025-03-07
r-signac public A framework for the analysis and exploration of single-cell chromatin data. The 'Signac' package contains functions for quantifying single-cell chromatin data, computing per-cell quality control metrics, dimension reduction and normalization, visualization, and DNA sequence motif analysis. Reference: Stuart and Butler et al. (2019) <doi:10.1016/j.cell.2019.05.031>. 2025-03-07
cctk public Tools to identify and compare CRISPR arrays. 2025-03-07
r-psminer public Utilities for interacting with the pathogensurveillance pipeline. 2025-03-07
busco public Assessment of assembly completeness using Universal Single Copy Orthologs. 2025-03-07
omark public OMArk - Proteome quality assesment based on OMAmer placements 2025-03-07
perl-bio-phylo-forest-dbtree public DBIx::Class-backed, Bio::Phylo-like API for large phylogenies. 2025-03-07
wfmash public a pangenome-scale aligner 2025-03-07
te-aid public Annotation helper tool for the manual curation of transposable element consensus sequences 2025-03-07
bioblend public A Python library for interacting with the Galaxy API. 2025-03-07
hmftools-cuppa public Predict tissue of origin for tumor samples from WGTS data. 2025-03-07
pegas public PeGAS is a Snakemake pipeline for genome analysis 2025-03-07
snakemake-executor-plugin-kubernetes public A snakemake executor plugin for submission of jobs to Kubernetes 2025-03-07
ebolaseq public Tool for downloading and analyzing Ebola virus sequences 2025-03-07
bioconductor-dada2 public Accurate, high-resolution sample inference from amplicon sequencing data 2025-03-07
centrifuger public Lossless compression of microbial genomes for efficient and accurate metagenomic sequence classification. 2025-03-07
resistify public A resistance gene annotation tool. 2025-03-07
plannotate public Webserver and command line tool for annotating engineered plasmids 2025-03-07
viroconstrictor public ViroConstrictor is a flexible pipeline for analysis of targeted viral sequencing data 2025-03-07
snp2cell public A package for finding enriched regulatory networks from GWAS and single cell data. 2025-03-07
savana public SAVANA: a somatic structural variant caller for long-read data 2025-03-07
bioconductor-glmgampoi public Fit a Gamma-Poisson Generalized Linear Model 2025-03-06
gmap-fusion public GMAP-fusion is a utility for identifying candidate fusion transcripts based on transcript sequences reconstructed via RNA-Seq de novo transcriptome assembly. 2025-03-06
transdecoder public TransDecoder identifies candidate coding regions within transcript sequences, such as those generated by de novo RNA-Seq transcript assembly using Trinity, or constructed based on RNA-Seq alignments to the genome using Tophat and Cufflinks. 2025-03-06
fusion-filter public FusionFilter provides a common fusion-finding, filtering, and annotation framework for the Trinity Cancer Transcriptome Analysis Toolkit (CTAT). 2025-03-06
fusion-inspector public FusionInspector is a component of the Trinity Cancer Transcriptome Analysis Toolkit (CTAT). FusionInspector assists in fusion transcript discovery by performing a supervised analysis of fusion predictions, attempting to recover and re-score evidence for such predictions. - https://github.com/FusionInspector/FusionInspector/wiki 2025-03-06
flexynesis public A deep-learning-based multi-omics bulk sequencing data integration suite with a focus on (pre-)clinical endpoint prediction. 2025-03-06

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