About Anaconda Help Download Anaconda

bioconda / packages

Package Name Access Summary Updated
gapless public gapless assembly improvement tool 2025-04-22
asgal public A graph aligner 2025-04-22
pangu public CYP2D6 PGx caller for PacBio HiFi Data 2025-04-22
querynator public Python package to query cancer variant databases 2025-04-22
spec2vec public Word2Vec based similarity measure of mass spectrometry data. 2025-04-22
pynteny public Multiple HMM - search via synteny structures in Python 2025-04-22
perl-bio-rna-barriers public Parse, query and manipulate output of Barriers 2025-04-22
perl-bio-rna-barmap public Parse and query BarMap mappings. 2025-04-22
perl-bio-rna-treekin public Classes for working with Treekin output. 2025-04-22
genomics-data-index public Indexes genomics data (nucleotide variants, kmers, MLST) for fast querying of features. 2025-04-22
sga_ice public Iterative error correction of long 250 or 300 bp Illumina reads minimizes the total amount of erroneous reads, which improves contig assembly 2025-04-22
cesar public CESAR 2.0 is a method to realign coding exons or genes to DNA sequences using a Hidden Markov Model 2025-04-22
forwardgenomics public Forward Genomics is a framework to associate phenotypic differences between species to differences in their genomes 2025-04-22
rerconverge public RERconverge is a set of software written in R that estimates the correlation between relative evolutionary rates of gene. 2025-04-22
rock public ROCK - Reducing Over-Covering K-mers 2025-04-22
strucvis public strucVis : Display small RNA depth of coverage on a predicted RNA secondary structure 2025-04-22
kingfisher public Download/extract biological FASTA/Q read data and metadata 2025-04-22
clinvar-this public ClinVar Submission API Made Easy. 2025-04-22
smncopynumbercaller public Call copy number of SMN1, SMN2, and SMN2Δ7–8 from a BAM file. 2025-04-22
gsea public Gene Set Enrichment Analysis (GSEA) 2025-04-22
tiny-count public \ A precision counting tool for hierarchical classification and quantification of small RNA-seq reads. tiny-count is part of the tinyRNA analysis pipeline. 2025-04-22
blend-bio public BLEND is a Fast, Memory-Efficient, and Accurate Mechanism to Find Fuzzy Seed Matches in Genome Analysis 2025-04-22
stare-abc public Calculate Gene-TF affinities via enhancer-gene interactions 2025-04-22
coverageanomalyscanner public Application to find local anomalies in read coverage and to predict putative SV events. 2025-04-22
pseudo-it public Reference-based genome assembly with iterative mapping 2025-04-22

© 2025 Anaconda, Inc. All Rights Reserved. (v4.2.2) Legal | Privacy Policy