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bioconda / packages

Package Name Access Summary Updated
tracy public Basecalling, alignment, assembly and deconvolution of Sanger chromatogram trace files 2025-08-04
rscape public R-scape (RNA Structural Covariation Above Phylogenetic Expectation) looks for evidence of a conserved RNA secondary structure by measuring pairwise covariations observed in an input multiple sequence alignment. 2025-08-04
sickle-trim public Windowed Adaptive Trimming for fastq files using quality 2025-08-04
bifrost public Highly parallel construction and indexing of colored and compacted de Bruijn graphs 2025-08-04
libgff public A simple "libraryfication" of the GFF/GTF parsing code that is used in GFFRead codebase. 2025-08-04
slow5tools public Toolkit for S/bLOW5 format 2025-08-04
cooltools public Analysis tools for genomic interaction data stored in .cool format 2025-08-04
unicycler public Hybrid assembly pipeline for bacterial genomes 2025-08-04
yacrd public Yet Another Chimeric Read Detector, with long-read mapper result as input. 2025-08-04
perl-text-balanced public Extract delimited text sequences from strings. 2025-08-04
prophyle public ProPhyle is an accurate, resource-frugal and deterministic phylogeny-based metagenomic classifier. 2025-08-04
amira public A tool to detect acquired AMR genes directly from long read sequencing data. 2025-08-04
krakentools public KrakenTools scripts for analysis of Kraken/KrakenUniq/Kraken2/Bracken results 2025-08-02
perl-bio-samtools public Read SAM/BAM files 2025-08-01
enabrowsertools public enaBrowserTools is a set of scripts that interface with the ENA web services to download data from ENA easily. 2025-08-01
perl-html-tidy public (X)HTML validation in a Perl object 2025-08-01
rtk public rtk - rarefaction toolkit for OTU tables 2025-08-01
ontime public Extract subsets of ONT (Nanopore) reads based on time 2025-08-01
impg public impg: implicit pangenome graphs. 2025-08-01
emblmygff3 public An efficient way to convert gff3 annotation files into EMBL format ready to submit. 2025-08-01
clair3-illumina public Clair3 with libraries to support variant calling using Illumina short-reads. Version in sync with Clair3. 2025-08-01
clair3 public Clair3 is a small variant caller for long-reads. Compare to PEPPER (r0.4), Clair3 (v0.1) shows a better SNP F1-score with ≤30-fold of ONT data (precisionFDA Truth Challenge V2), and a better Indel F1-score, while runs generally four times faster. Clair3 makes the best of both worlds of using pileup or full-alignment as input for deep-learning based long-read small variant calling. Clair3 is simple and modular for easy deployment and integration. 2025-08-01
seqfu public DNA sequence utilities 2025-08-01
oligomap public Oligomap is a program for fast identification of nearly-perfect matches of small RNAs in sequence databases. 2025-08-01
stereogene public StereoGene: Rapid Estimation of Genomewide Correlation of Continuous or Interval Feature Data 2025-08-01

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