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bioconda / packages

Package Name Access Summary Updated
perl-gd-svg public Seamlessly enable SVG output from scripts written using GD 2023-06-16
kcalign public Kalgin-based codon-aware aligner for multiple sequences 2023-06-16
readucks public Readucks: a simple demultiplexer for nanopore reads 2023-06-16
riboseqc public Read length specific QC of Ribo-seq data 2023-06-16
rkp public Relative K-mer Project 2023-06-16
r-transphylo public Reconstruction of transmission trees using genomic data 2023-06-16
rnabloom public Java tool for RNA-seq assembly 2023-06-16
yapc public Yapc is a (yet another) peak caller for genomic high-throughput sequencing data 2023-06-16
tadbit public TADbit is a complete Python library to deal with all steps to analyze, model and explore 3C-based data. 2023-06-16
callstate public A replacement for GATK3 CallableLoci 2023-06-16
coral public Coral is an efficient tool to bridge paire-end RNA-seq reads. 2023-06-16
sigmut public Wrapper of SigProfiler (Copyright(c) 2019, Erik Bergstrom [Alexandrov Lab]) 2023-06-16
sicer2 public Redesigned and improved ChIP-seq broad peak calling tool SICER. 2023-06-16
pyslim public Manipulate tree sequences produced by SLiM. 2023-06-16
pgx-pipe-helper public A helper module for wrapping functionality which is common to all pipeline stages. 2023-06-16
phylics public Single-cell CNV data analysis toolkit 2023-06-16
phastaf public Identify phage regions in bacterial genomes for masking purposes 2023-06-16
conterminator public Conterminator: software to detect contamination in large sequence sets 2023-06-16
pgx-variant-tools public This library contains various methods and utilities for the calling and manipulation of normalized variants. 2023-06-16
enrichm public EnrichM is a toolbox for comparing the functional composition of population genomes 2023-06-16
kofamscan public KofamKOALA assigns K numbers to the user's sequence data by HMMER/HMMSEARCH against KOfam 2023-06-16
galaxy-util public Galaxy Generic Utilities 2023-06-16
galaxy-tool-util public Galaxy Tool and Tool Dependency Utilities 2023-06-16
galaxy-containers public Galaxy Container Modeling and Interaction Abstractions 2023-06-16
r-qtl2 public R/qtl2 provides a set of tools to perform quantitative trait locus (QTL) analysis in experimental crosses. It is a reimplementation of the R/qtl package to better handle high-dimensional data and complex cross designs. This package is designed to make it easy to install and load multiple R/qtl2 packages in a single step. Broman et al. (2018) <doi:10.1534/genetics.118.301595>. 2023-06-16
crisprbact public Tools to design and analyse CRISPRi experiments 2023-06-16
perl-text-csv_xs public Text::CSV_XS - comma-separated values manipulation routines 2023-06-16
clan public CLAN - the CrossLinked reads ANalysis tool 2023-06-16
vsnp public Rapidly call, validate, and compare SNPs from FASTQ files in a timely manner utilizing large data sets. 2023-06-16
chira public An integrated framework for annotation and visualization of chimeric reads. 2023-06-16
locus_processing public Tools for working with locus definition files 2023-06-16
pp-sketchlib public Library of sketching functions used by PopPUNK 2023-06-16
quantwiz-iq public QuantWiz-IQ is a tool for reporter based MS/MS quantitation using iTRAQ or TMT tags from shotgun proteomics experiments. 2023-06-16
biotdg public Bioinformatics Test Data Generator 2023-06-16
imsindel public An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis 2023-06-16
chromosight public Detect loops (and other patterns) in Hi-C contact maps. 2023-06-16
interleafq public Interleave and deinterleave FASTQ files 2023-06-16
shannon_cpp public shannon_cpp is command line tool for denovo rna assembly 2023-06-16
hypo public Super Fast and Accurate Polisher for Long Read Genome Assemblies. 2023-06-16
libis public Low input Bisulfite sequencing alignment 2023-06-16
rsat-core public Detection of regulatory signals in non-coding sequences. 2023-06-16
haploconduct public HaploConduct is a package designed for reconstruction of individual haplotypes from next generation sequencing data, in particular Illumina. It provides two methods, SAVAGE and POLYTE, which can be run through the haploconduct wrapper. 2023-06-16
perl-math-matrixreal public Manipulate NxN matrices of real numbers 2023-06-16
perl-math-matrix public Multiply and invert Matrices 2023-06-16
cameo public cameo - computer aided metabolic engineering & optimization 2023-06-16
openms-tools public OpenMS is an open-source software C++ library for LC-MS data management and analyses 2023-06-16
luciphor2 public Luciphor2 performs PTM-site localization on MS/MS data 2023-06-16
libis_moabs public Low input Bisulfite sequencing alignment 2023-06-16
ncbimeta public Efficient and comprehensive metadata acquisition from the NCBI databases (includes SRA). 2023-06-16
hypercluster public A package for automatic clustering hyperparameter optmization 2023-06-16

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