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Package Name Access Summary Updated
dimspy public Python package for data processing of direct-infusion mass spectrometry-based metabolomics and lipidomics data 2023-06-16
r-phylobase public Provides a base S4 class for comparative methods, incorporating one or more trees and trait data. 2023-06-16
r-oai public A general purpose client to work with any 'OAI-PMH' (Open Archives Initiative Protocol for 'Metadata' Harvesting) service. The 'OAI-PMH' protocol is described at <http://www.openarchives.org/OAI/openarchivesprotocol.html>. Functions are provided to work with the 'OAI-PMH' verbs: 'GetRecord', 'Identify', 'ListIdentifiers', 'ListMetadataFormats', 'ListRecords', and 'ListSets'. 2023-06-16
r-rbison public Interface to the 'USGS' 'BISON' (<https://bison.usgs.gov/>) 'API', a 'database' for species occurrence data. Data comes from species in the United States from participating data providers. You can get data via 'taxonomic' and location based queries. A simple function is provided to help visualize data. 2023-06-16
r-ecodist public Dissimilarity-based analysis functions including ordination and Mantel test functions, intended for use with spatial and community data. 2023-06-16
r-rvertnet public Retrieve, map and summarize data from the 'VertNet.org' archives (<http://vertnet.org/>). Functions allow searching by many parameters, including 'taxonomic' names, places, and dates. In addition, there is an interface for conducting spatially delimited searches, and another for requesting large 'datasets' via email. 2023-06-16
r-ridigbio public An interface to iDigBio's search API that allows downloading specimen records. Searches are returned as a data.frame. Other functions such as the metadata end points return lists of information. iDigBio is a US project focused on digitizing and serving museum specimen collections on the web. See <https://www.idigbio.org> for information on iDigBio. 2023-06-16
r-geoaxe public Split 'geospatial' objects into pieces. Includes support for some spatial object inputs, 'Well-Known Text', and 'GeoJSON'. 2023-06-16
illumiprocessor public illumiprocessor is a tool to batch process illumina sequencing reads using the excellent trimmomatic package. 2023-06-16
r-wicket public Utilities to generate bounding boxes from 'WKT' (Well-Known Text) objects and R data types, validate 'WKT' objects and convert object types from the 'sp' package into 'WKT' representations. 2023-06-16
r-adephylo public Multivariate tools to analyze comparative data, i.e. a phylogeny and some traits measured for each taxa. 2023-06-16
snpsplit public SNPsplit is an allele-specific alignment sorter which is designed to read in alignment files in SAM/BAM format and determine the allelic origin of reads that cover known SNP positions. 2023-06-16
womtool public Command line utilities for interacting with WDL 2023-06-16
real public REad ALigner for Next-Generation sequencing reads. 2023-06-16
r-propcis public Computes two-sample confidence intervals for single, paired and independent proportions. 2023-06-16
bsmap public BSMAP is a short reads mapping software for bisulfite sequencing reads. 2023-06-16
ngmerge public Merging paired-end reads and removing sequencing adapters. 2023-06-16
cortex_con public cortex_con (primary contact Mario Caccamo) is for consensus genome assembly 2023-06-16
esimsa public Simple deconvolution of electrospray ionization peak lists 2023-06-16
idr-py public Helper methods for accessing the Image Data Resource (IDR) 2023-06-16
spotyping public SpoTyping: fast and accurate in silico Mycobacterium spoligotyping from sequence reads 2023-06-16
blobtools public Modular command-line solution for visualisation, quality control and taxonomic partitioning of genome datasets 2023-06-16
cdna_cupcake public cDNA_Cupcake is a miscellaneous collection of Python and R scripts used for analyzing sequencing data. 2023-06-16
riboraptor public Python package to analyse ribosome profiling data 2023-06-16
erds public Inferring copy number variants in high-coverage human genomes with next-generation sequencing data. 2023-06-16
r-genometricorr public Genometric Correlation (GenometriCorr) is an R package for spatial correlation of genome-wide interval datasets. 2023-06-16
ctat-lncrna public ctat-lncrna uses slncky 2023-06-16
realphy public The Reference sequence Alignment based Phylogeny 2023-06-16
r-fmsb public Several utility functions for the book entitled "Practices of Medical and Health Data Analysis using R" (Pearson Education Japan, 2007) with Japanese demographic data and some demographic analysis related functions. 2023-06-16
jali public Alignment method for comparing a protein sequence to a protein family, represented by a multiple alignment. It can also be used for sensitive protein database searches. The algorithm is a generalization of the Smith-Waterman algorithm. 2023-06-16
biopet-vcfstats public Vcfstats is a tool that can generate metrics from a vcf file. 2023-06-16
bibliospec public The BiblioSpec Spetral Library tool suite 2023-06-16
perl-extutils-cbuilder public Compile and link C code for Perl modules 2023-06-16
mmvc public Call variants based on a Bayesian multinomial mixture model. 2023-06-16
ruby-dna-tools public Various libraries containing useful functions for working with DNA sequences, written in ruby. Some tools are not specific to DNA. 2023-06-16
pbhoover public Variant caller for legacy and low coverage Pacific Biosciences' long-read sequencing data 2023-06-16
perl-extutils-constant public generate XS code to import C header constants 2023-06-16
perl-perl4-corelibs public libraries historically supplied with Perl 4 2023-06-16
ac-diamond public AC-DIAMOND is a DNA-protein alignment tool 2023-06-16
r-stampp public Allows users to calculate pairwise Nei's Genetic Distances (Nei 1972), pairwise Fixation Indexes (Fst) (Weir & Cockerham 1984) and also Genomic Relationship matrixes following Yang et al. (2010) in mixed and single ploidy populations. Bootstrapping across loci is implemented during Fst calculation to generate confidence intervals and p-values around pairwise Fst values. StAMPP utilises SNP genotype data of any ploidy level (with the ability to handle missing data) and is coded to utilise multithreading where available to allow efficient analysis of large datasets. StAMPP is able to handle genotype data from genlight objects allowing integration with other packages such adegenet. Please refer to LW Pembleton, NOI Cogan & JW Forster, 2013, Molecular Ecology Resources, 13(5), 946-952. <doi 2023-06-16
rnaclust public A tool for clustering of RNAs based on their secondary structures using LocARNA 2023-06-16
vqsr_cnn public Variant quality score recalibration with Convolutional Neural Networks 2023-06-16
hanselx public A graph-inspired data structure for determining likely chains of sequences from breadcrumbs of evidence 2023-06-16
brockman-pipeline public Brockman Representation Of Chromatin by K-mers in Mark-Associated Nucleotides 2023-06-16
amused public Auditing Motifs Using Statistical Enrichment & Depletion 2023-06-16
gretel public An algorithm for recovering haplotypes from metagenomes 2023-06-16
comparative-annotation-toolkit public A straightforward end-to-end pipeline that takes as input a HAL-format multiple whole genome alignment as well as a GFF3 file representing annotations on one high quality assembly in the HAL alignment, and produces a output GFF3 annotation on all target genomes chosen 2023-06-16
segtools public a python package for analyzing genomic segmentations 2023-06-16
assemblerflow public A Nextflow pipeline assembler for genomics. Pick your modules. Assemble them. Run the pipeline. 2023-06-16
satsuma2 public FFT cross-correlation based synteny aligner, (re)designed to make full use of parallel computing 2023-06-16

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