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bioconda / packages

Package Name Access Summary Updated
r-spp public Analysis of ChIP-seq and other functional sequencing data [Kharchenko PV (2008) <DOI:10.1038/nbt.1508>]. 2025-09-16
fraggenescan public FragGeneScan is an application for finding (fragmented) genes in short reads. 2025-09-16
elprep public elPrep is a high-performance tool for preparing .sam/.bam files for variant calling in sequencing pipelines. It can be used as a drop-in replacement for SAMtools/Picard/GATK4. 2025-09-16
bamm public Metagenomics-focused BAM file manipulation 2025-09-16
perl-math-base-convert public Very fast base to base conversion. 2025-09-16
gmap public Genomic mapping and alignment program for mRNA and EST sequences. 2025-09-15
sonicparanoid public SonicParanoid: fast, accurate, and comprehensive orthology inference with machine learning and language models 2025-09-15
perl-mime-types public Definition of MIME types 2025-09-15
perl-libwww-perl public The World-Wide Web library for Perl. 2025-09-14
vcf2maf public Convert a VCF into a MAF where each variant is annotated to only one of all possible gene isoforms. 2025-09-13
eggnog-mapper public Fast genome-wide functional annotation through orthology assignment. 2025-09-13
gseapy public Gene Set Enrichment Analysis in Python. 2025-09-13
perl-excel-writer-xlsx public Create a new file in the Excel 2007+ XLSX format. 2025-09-13
gtdbtk public A toolkit for assigning objective taxonomic classifications to bacterial and archaeal genomes. 2025-09-12
perl-mce public Many-Core Engine for Perl providing parallel processing capabilities 2025-09-10
perl-image-exiftool public ExifTool is a platform-independent Perl library plus a command-line application for reading, writing and editing meta information in a wide variety of files. 2025-09-10
addrg public No Summary 2025-09-10
rascaf public Scaffolding with RNA-seq read alignment. 2025-09-10
pathoscope public Species identification and strain attribution with unassembled sequencing data 2025-09-10
splicemap public Detects splice junctions from RNA-seq data. This method does not depend on any existing annotation of gene structures and is capable of finding novel splice junctions with high sensitivity and specificity. It can handle long reads (50–100 nt) and can exploit paired-read information to improve mapping accuracy. 2025-09-10
hardklor public Analyze mass spectra 2025-09-10
gxformat2 public Galaxy Workflow Format 2 Descriptions. 2025-09-10
antismash public antiSMASH - the antibiotics and Secondary Metabolite Analysis SHell. 2025-09-09
trimadap public Fast but inaccurate adapter trimmer for Illumina reads. 2025-09-09
fermikit public No Summary 2025-09-09

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