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bioconda / packages

Package Name Access Summary Updated
metaphlan public Metagenomic Phylogenetic Analysis. 2025-06-04
pretextsnapshot public Commandline image generator for Pretext Hi-C genome contact maps. 2025-06-04
bowtie2 public A fast and sensitive gapped read aligner. 2025-06-03
r-tmae public Tests and visualizations for mono-allelicly expressed variants. 2025-06-03
bcftools-liftover-plugin public Tools to work with GWAS-VCF summary statistics files (liftover plugin only) 2025-06-03
k8 public Lightweight JavaScript shell based on Google's V8 JavaScript engine 2025-06-03
quota_anchor public Strand and WGD aware syntenic gene identification 2025-06-03
iced public The python module iced implements the ICE normalization of hic data. 2025-06-03
rustybam public Mitchell Vollger's bioinformatics rust utilities. 2025-06-03
vqbg public De Novo Reconstruction of Viral Quasispecies from Bubble Graph 2025-06-03
rucs public RUCS is a bioinformatics tool developed to ease the task of designing new primers. 2025-06-03
riboloco public Riboseq analysis. 2025-06-03
transit public TRANSIT 2025-06-02
uniprot-id-mapper public A Python wrapper for the UniProt Mapping RESTful API. 2025-06-02
r-tinc public TINC is a package that implements algorithms to determine the contamination of a bulk sequencing sample in the context of cancer studies (matched tumour/ normal). The contamination estimated by TINC can be either due to normal cells sampled in the tumour biopsy or to tumour cells in the normal biopsy. The former case is traditionally called purity, or cellularity, and a number of tools exist to estimate it. The latter case is less common, and that is the main reason TINC has been developed. For this reason, the package takes name TINC, Tumour-in-Normal contamination. TINC is part of the evoverse, a package that gathers multiple R packages to implement Cancer Evolution analyses. 2025-06-02
longtrack public Track FMT strains using long-read metagenomic assemblies. 2025-06-02
freebayes public Bayesian haplotype-based polymorphism discovery and genotyping. 2025-06-02
diatracer public A diaPASEF spectrum-centric analysis tool 2025-06-02
fgsmk public Supporting functions for running Snakemake workflows. 2025-06-02
pytwobit public A fast reader for local or remote UCSC twobit sequence files. 2025-06-02
pdbx public A parser module in python for structures of the protein data bank in the mmcif format 2025-06-02
vafator public VAFator annotates the variants in a VCF file with technical annotations extracted from one or more BAM alignment files. We implement a set of basic coverage annotations and also more sophisticated published annotations used to assess the quality of every variant call. 2025-06-02
mmcif public mmCIF Core Access Library 2025-06-02
bioconductor-dirichletmultinomial public Dirichlet-Multinomial Mixture Model Machine Learning for Microbiome Data 2025-06-02
vcfx public VCFX: A Comprehensive VCF Manipulation Toolkit 2025-06-02

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