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Package Name Access Summary Updated
flextaxd public Script that allows the creation of custom kraken databases from various sources (NCBI, QIIME, CanSNPer) 2023-06-16
whatsgnu public WhatsGNU A Tool For Identifying Proteomic Novelty 2023-06-16
biowdl-input-converter public Converting various input formats into WDL structs for BioWDL pipelines. 2023-06-16
cigar public manipulate SAM cigar strings 2023-06-16
seacr public SEACR is intended to call peaks and enriched regions from sparse CUT&RUN or chromatin profiling data in which background is dominated by "zeroes" (i.e. regions with no read coverage). It requires R (https://www.r-project.org) and Bedtools (https://bedtools.readthedocs.io/en/latest/) to be available in your path, and it requires bedgraphs from paired-end sequencing as input, which can be generated from read pair BED files (i.e. BED coordinates reflecting the 5' and 3' termini of each read pair) using bedtools genomecov with the "-bg" flag, or alternatively from name-sorted paired-end BAM files as described in "Preparing input bedgraph files" below. 2023-06-16
mavis public A Structural Variant Post-Processing Package 2023-06-16
perl-data-lock public makes variables (im)?mutable 2023-06-16
primerclip public Swift Accel-Amplicon primer trimming tool for fast alignment-based primer trimming 2023-06-16
samstats public SAM file alignment statistics at the read level 2023-06-16
encyclopedia public EncyclopeDIA is library search engine comprised of several algorithms for DIA data analysis 2023-06-16
perl-http-tiny public A small, simple, correct HTTP/1.1 client 2023-06-16
vpolo public Support package for Alevin tools 2023-06-16
patholive public A real-time pathogen diagnostics tool for metagenomic Illumina sequencing data. 2023-06-16
tagore public A simple way to visualize features on human chromosome ideograms 2023-06-16
umap public Umap and Bismap: tools for genome and methylome mappability 2023-06-16
salmid public Rapid tool to check taxonomic ID of single isolate samples. Currently only IDs Salmonella species and subspecies, and some common contaminants (Listeria, Escherichia). 2023-06-16
python-eel public Tool for finding evolutionarily conserved mammalian enhancer elements. 2023-06-16
xpressplot public A toolkit for navigating and analyzing gene expression datasets. 2023-06-16
panpasco public Pipeline for pangenome mapping and pairwise SNP distance 2023-06-16
fings public Filters for Next Generation Sequencing 2023-06-16
blksheep public A package for differential extreme values analysis 2023-06-16
traitar public traitar - The microbial trait analyzer 2023-06-16
kggseq public KGGSeq is a software platform constituted of Bioinformatics and statistical genetics functions making use of valuable biologic resources and knowledge for sequencing-based genetic mapping of variants/genes responsible for human diseases/traits. 2023-06-16
atlas-metadata-validator public A MAGE-TAB validator for Expression Atlas and Single Cell Expression Atlas 2023-06-16
sepp-refgg138 public SATe-enabled phylogenetic placement 2023-06-16
rop public The Read Origin Protocol (ROP) is a computational protocol that aims to discover the source of all reads, including those originating from repeat sequences, recombinant B and T cell receptors, and microbial communities. 2023-06-16
sepp-refsilva128 public SATe-enabled phylogenetic placement 2023-06-16
svanalyzer public SVanalyzer: tools for the analysis of structural variation in genomes 2023-06-16
ena-dl public A tool to download FASTQs associated with Study, Experiment, or Run accessions. 2023-06-16
calib public Clustering without alignment using (locality sensitive hashing) LSH and MinHashing of barcoded reads 2023-06-16
jmztab-m public This project is the reference reader, writer and validator implementation for mzTab for metabolomics 2.0+. 2023-06-16
emmtyper public Streptococcus pyogenes in silico EMM typer 2023-06-16
monocle3-cli public A set of wrappers for individual components of the monocle3 package. Functions R packages are hard to call when building workflows outside of R, so this package adds a set of simple wrappers with robust argument parsing. Intermediate steps are currently monocle3 R objects, but the ultimate objective is to have language-agnostic intermediate formats allowing composite workflows using a variety of software packages. 2023-06-16
aquila public Diploid personal genome assembly and comprehensive variant detection based on linked-reads 2023-06-16
jupyterngsplugin public Jupyter notebook plugin Bioinformatics NGS data analysis 2023-06-16
extract_fasta_seq public To extract specific fasta sequences from a fasta file. 2023-06-16
msaconverter public To convert multiple alignment alignments (MSA) into different formats 2023-06-16
python-goenrichment public GO enrichment analysis from a list of gene names using a precomputed database 2023-06-16
taxonomy_ranks public To get taxonomy ranks information for taxid, species name, or higher ranks (e.g., genus, family) with ETE3 from NCBI Taxonomy database. 2023-06-16
bold-identification public A tool for taxonomic assignment for given sequences using the BOLD database (http://www.boldsystems.org/index.php) 2023-06-16
extract-codon-alignment public To extract some codon positions (1st, 2nd, 3rd) from a CDS alignment. 2023-06-16
ega2 public EGA download client v2 2023-06-16
logomaker public Package for making Sequence Logos 2023-06-16
aquila_umap public This is a program to generate Umap for Aquila diploid assembly. 2023-06-16
motifraptor public Motif-centric analysis on GWAS data 2023-06-16
pynnotator public A Python Annotation Framework for VCFs using multiple tools. 2023-06-16
uvp public A Unified Variant Pipeline to identify variants and assign lineage from MTBC sequence data. 2023-06-16
kounta public Generate multi-sample k-mer count matrix 2023-06-16
aquila_stlfr public Diploid assembly and variants calling for stLFR and hybrid assembler for both linked-reads. 2023-06-16
vmatch public The Vmatch large scale sequence analysis software 2023-06-16

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