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bioconda / packages

Package Name Access Summary Updated
switchtfi public Implementation of the SwitchTFI method as presented in: https://doi.org/10.1101/2025.01.20.633856 2025-09-23
cagecleaner public Genomic redundancy removal tool for cblaster hit sets. 2025-09-23
gap2seq public Gap2Seq is a tool for filling gaps between contigs in genome assemblies. 2025-09-23
ltr_finder public LTR_Finder is an efficient program for finding full-length LTR retrotranspsons in genome sequences. 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
altex-be public Automatically design sgRNA for exon skipping with many base editors. 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
funannotate public funannotate: eukaryotic genome annotation pipeline 2025-09-23
discosnp public reference-free small variant caller for short read sequencing data 2025-09-23
cactus public Cactus is a reference-free whole-genome multiple alignment program based upon notion of Cactus graphs 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
mindthegap public MindTheGap performs detection and assembly of DNA insertion variants in NGS read datasets with respect to a reference genome. MindTheGap can also be used as a genome assembly finishing tool, it can fill the gaps between a set of input contigs without any a priori on their relative order and orientation. 2025-09-23
short-read-connector public Short read connector enables the comparisons of two read sets 2025-09-23
upimapi public UniProt Id Mapping through API 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
generax public GeneRax: a parallel tool for species tree-aware maximum likelihood based gene tree inference under gene duplication, transfer, and loss. 2025-09-22
physher public A multi-algorithmic framework for phylogenetic inference 2025-09-22
r-stitch public STITCH - Sequencing To Imputation Through Constructing Haplotypes. 2025-09-22
b2btools public The bio2Byte software suite to predict protein biophysical properties 2025-09-22
fasta3 public The FASTA package - protein and DNA sequence similarity searching and alignment programs 2025-09-22
savana public SAVANA: a somatic structural variant caller for long-read data. 2025-09-22

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