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bioconda / packages

Package Name Access Summary Updated
gap2seq public Gap2Seq is a tool for filling gaps between contigs in genome assemblies. 2025-09-23
sga public SGA - String Graph Assembler. SGA is a de novo assembler for DNA sequence reads. It is based on Gene Myers string graph formulation of assembly and uses the FM-index/Burrows-Wheeler transform to efficiently find overlaps between sequence reads. 2025-09-23
snpeff public Genetic variant annotation and effect prediction toolbox 2025-09-23
snpsift public Toolbox that allows you to filter and manipulate annotated files 2025-09-23
discosnp public reference-free small variant caller for short read sequencing data 2025-09-23
assembly-stats public Get assembly statistics from FASTA and FASTQ files 2025-09-23
treebest public TreeBeST: Tree Building guided by Species Tree, used in the Ensembl Compara pipeline. 2025-09-23
samtools public Tools for dealing with SAM, BAM and CRAM files 2025-09-23
fastuniq public No Summary 2025-09-23
dsk public DSK is a k-mer counter for reads or genomes. 2025-09-22
r-stitch public STITCH - Sequencing To Imputation Through Constructing Haplotypes. 2025-09-22
fasta3 public The FASTA package - protein and DNA sequence similarity searching and alignment programs 2025-09-22
glimmerhmm public No Summary 2025-09-22
visceral-evaluatesegmentation public EvaluateSegmentation is a tool that compares two volumes (a test segmentation and a ground truth segmentation) using 22 different metrics that were selected as a result of a comprehensive research into the metrics used in the medical volume segmentations. 2025-09-22
survivor public Toolset for SV simulation, comparison and filtering 2025-09-21
expansionhunter public A tool for estimating repeat sizes 2025-09-21
vt public A tool set for short variant discovery in genetic sequence data 2025-09-21
concoct public Clustering cONtigs with COverage and ComposiTion 2025-09-20
samsift public Advanced filtering and tagging of SAM/BAM alignments using Python expressions. 2025-09-19
ngs-disambiguate public Disambiguation algorithm for reads aligned to human and mouse genomes using Tophat or BWA mem 2025-09-19
snp-dists public Convert a FASTA alignment to SNP distance matrix 2025-09-19
smalt public SMALT aligns DNA sequencing reads with a reference genome. 2025-09-18
edena public No Summary 2025-09-18
rust-bio-tools public A growing collection of fast and secure command line utilities for dealing with NGS data implemented on top of Rust-Bio. 2025-09-18
abyss public Assembly By Short Sequences - a de novo, parallel, paired-end short read sequence assembler. 2025-09-18

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