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bioconda / packages

Package Name Access Summary Updated
pytantan public Cython bindings and Python interface to Tantan, a fast method for identifying repeats in DNA and protein sequences. 2025-07-16
anospp-analysis public ANOSPP data analysis 2025-07-16
plateo public Read/write microplate and picklist data for lab automation 2025-07-16
staden_io_lib public Staden io_lib is a library of file reading and writing code e.g. for SAM/BAM/CRAM. 2025-07-16
coverm public CoverM aims to be a configurable, easy to use and fast DNA read coverage and relative abundance calculator focused on metagenomics applications 2025-07-16
pcangsd public Framework for analyzing low-depth next-generation sequencing (NGS) data in heterogeneous/structured populations using principal component analysis (PCA). 2025-07-16
mapdamage2 public mapDamage: tracking and quantifying damage patterns in ancient DNA sequencing reads generated by Next-Generation Sequencing platforms. 2025-07-16
automappa public Automappa: An interactive interface for exploration of metagenomes. 2025-07-15
famsa public Algorithm for large-scale multiple sequence alignments. 2025-07-15
codoff public codoff: program to measure the irregularity of the codon usage for a single genomic region (e.g. a BGC, phage, etc.) relative to the full genome. 2025-07-15
kleborate public Kleborate: a tool for typing and screening pathogen genome assemblies. 2025-07-15
hgvs public HGVS Parser, Formatter, Mapper, and Validator. 2025-07-15
tower-cli public The Tower CLI an interface to Nextflow Tower via the CLI. 2025-07-15
r-pathfindr public Enrichment analysis enables researchers to uncover mechanisms underlying a phenotype. However, conventional methods for enrichment analysis do not take into account protein-protein interaction information, resulting in incomplete conclusions. pathfindR is a tool for enrichment analysis utilizing active subnetworks. The main function identifies active subnetworks in a protein-protein interaction network using a user-provided list of genes and associated p values. It then performs enrichment analyses on the identified subnetworks, identifying enriched terms (i.e. pathways or, more broadly, gene sets) that possibly underlie the phenotype of interest. pathfindR also offers functionalities to cluster the enriched terms and identify representative terms in each cluster, to score the enriched terms per sample and to visualize analysis results. The enrichment, clustering and other methods implemented in pathfindR are described in detail in Ulgen E, Ozisik O, Sezerman OU. 2019. pathfindR: An R Package for Comprehensive Identification of Enriched Pathways in Omics Data Through Active Subnetworks. Front. Genet. <doi:10.3389/fgene.2019.00858>. 2025-07-15
seqnado public Pipelines for genomics analysis 2025-07-15
amdirt public amdirt: AncientMetagenomeDir Toolkit 2025-07-15
hgtools public Classes for Mercurial and Git repositories. 2025-07-15
tb-profiler public Profiling tool for Mycobacterium tuberculosis to detect drug resistance and lineage from sequencing data 2025-07-15
hits public Utilities for processing high-throughput sequencing experiments. 2025-07-15
gffcompare public GffCompare by Geo Pertea. 2025-07-15
biocommons.seqrepo public Python package for writing and reading a local collection of biological sequences. 2025-07-15
ebolaseq public Tool for downloading and analyzing Ebola virus sequences. 2025-07-15
aci public Visualizes coverage for amplicons. 2025-07-15
geofetch public Downloads data and metadata from GEO and SRA and creates standard PEPs. 2025-07-15
perl-inline public Write Perl Subroutines in Other Programming Languages. 2025-07-15

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