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bioconda / packages

Package Name Access Summary Updated
genome_profiler public Prokaryotic genome and plasmid profiling pipeline. 2025-07-03
repeatmodeler public RepeatModeler is a de-novo repeat family identification and modeling package. 2025-07-03
repeatafterme public A package for the extension of repetitive DNA sequences. 2025-07-03
domclust public Effective tool for orthologous grouping in multiple genomes 2025-07-03
beast public BEAST is a cross-platform program for Bayesian analysis of molecular sequences using MCMC. 2025-07-03
primer3-py public Python bindings for Primer3 2025-07-02
bwa-mem2 public The next version of bwa-mem. 2025-07-02
phasius public A rust tool to create phase-block maps from phased cram/bam files. 2025-07-02
r-lme4qtl public Linear mixed models (lme4) with flexible covariance structure for qtl and association analysis. 2025-07-02
panman public PanMAN 2025-07-02
rabies public RABIES: Rodent Automated Bold Improvement of EPI Sequences. 2025-07-02
nordic public NORDic: a Network-Oriented package for the Repurposing of Drugs 2025-07-02
endorspy public endorS.py calculates endogenous DNA from samtools flagstat files and print to screen. 2025-07-02
crispresso2 public A software pipeline designed to enable rapid and intuitive interpretation of genome editing experiments. 2025-07-02
phabox public Virus identification and analysis tool set 2025-07-02
lorax public A long-read analysis toolbox for cancer genomics 2025-07-02
replidec public Replication Cycle Decipher for Phages. 2025-07-02
fragpipe public Pipeline for comprehensive analysis of shotgun proteomics data 2025-07-02
hybpiper public HybPiper is a suite of Python scripts/modules for targeted sequence capture. 2025-07-02
ucsc-overlapselect public Select records based on overlapping chromosome ranges. 2025-07-02
qcatch public QCatch: Quality Control downstream of alevin-fry / simpleaf. 2025-07-02
ezomero public A module with convenience functions for writing Python code that interacts with OMERO. 2025-07-01
faststructure public A variational framework for inferring population structure from SNP genotype data. 2025-07-01
r-exomedepth public Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders. 2025-06-30
ucsc-facount public Count base statistics and CpGs in FA files. 2025-06-30

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