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bioconda / packages

Package Name Access Summary Updated
thapbi-pict public THAPBI Phytophthora ITS1 Classifier Tool (PICT). 2024-09-09
snakemake-executor-plugin-drmaa public A snakemake executor plugin for submission of jobs via DRMAA. 2024-09-09
snakemake-executor-plugin-kubernetes public A snakemake executor plugin for submission of jobs to Kubernetes 2024-09-09
binchicken public Targeted recovery of low abundance metagenome assembled genomes through intelligent coassembly 2024-09-09
biobox_add_taxid public CAMI amber utility script for adding the taxid output from GTDB and BAT 2024-09-08
clinvar-this public ClinVar Submission API Made Easy 2024-09-07
cogent3 public COmparative GENomics Toolkit 3: genomic sequence analysis within notebooks or on compute systems with 1000s of CPUs. 2024-09-06
scnic public SCNIC: Sparse Cooccurence Network Investigation for Compositional data 2024-09-06
piawka public The powerful AWK script to calculate population statistics in VCF files with support for varying ploidy and missing data 2024-09-06
ipyrad public Interactive assembly and analysis of RAD-seq data sets. 2024-09-06
egglib public Evolutionary Genetics and Genomics Library. EggLib is a C++/Python library and program package for evolutionary genetics and genomics. Main features are sequence data management, sequence polymorphism analysis, and coalescent simulations. EggLib is a flexible Python module with a performant underlying C++ library and allows fast and intuitive development of Python programs and scripts. 2024-09-06
treesimulator public Simulation of rooted phylogenetic trees under a given Multitype Birth–Death (MTBD) model. 2024-09-06
annonars public Genome annotation based on Rust and RocksDB. 2024-09-06
oakvar public OakVar - Genomic Variant Analysis Platform 2024-09-06
cami-amber public AMBER: Assessment of Metagenome BinnERs 2024-09-06
varvamp public Variable VirusAMPlicons (varVAMP) is a tool to design primers for highly diverse viruses 2024-09-06
shorttracks public ShortTracks : Useful length- and strand-based coverage files (bigwig) from small RNA-seq alignments (BAM) 2024-09-05
r-anndata public A 'reticulate' wrapper for the Python package 'anndata'. Provides a scalable way of keeping track of data and learned annotations. Used to read from and write to the h5ad file format. 2024-09-05
strucvis public strucVis : Display small RNA depth of coverage on a predicted RNA secondary structure 2024-09-05
starcatpy public Implements *CellAnnotator (aka *CAT/starCAT), annotating scRNA-Seq with predefined gene expression programs. 2024-09-05
handyreadgenotyper public Tool for training model and classifying reads from environmental ONT amplicon sequencing. 2024-09-05
annotsv public Annotation and Ranking of Structural Variation 2024-09-05
cagee public Analyzes changes in gene expression in a way that accounts for phylogenetic history and provides a statistical foundation for evolutionary inferences 2024-09-05
binette public A fast and accurate binning refinement tool to constructs high quality MAGs from the output of multiple binning tools. 2024-09-05
anchorwave public Sensitive alignment of genomes with high sequence diversity, extensive structural polymorphism, and whole-genome duplication variation 2024-09-05
python-edlib public Lightweight, super fast C/C++ (& Python) library for sequence alignment using edit (Levenshtein) distance. 2024-09-05
piranha-polio public Poliovirus Investigation Resource Automating Nanopore Haplotype Analysis 2024-09-05
allo public Multi-mapped read rescue strategy for gene regulatory analyses 2024-09-05
clipandmerge public Clip&Merge is a tool to clip off adapters from sequencing reads and merge overlapping paired end reads together. 2024-09-05
dedup public DeDup is a tool for read deduplication in paired-end read merging (e.g. for ancient DNA experiments). 2024-09-05
bcbio-gff public A Python library to read and write Generic Feature Format (GFF). 2024-09-05
flexi-formatter public Moving flexiplex barcode and UMI to bam tags 2024-09-05
medicc2 public Whole-genome doubling-aware copy number phylogenies for cancer evolution 2024-09-04
poplddecay public PopLDdecay: a fast and effective tool for linkage disequilibrium decay analysis based on variant call format (VCF) files. 2024-09-04
pyrodigal public Python bindings to Prodigal, an ORF finder for microbial sequences. 2024-09-04
beacon2-import public Seamlessly import and query genomic variant data from a beacon 2024-09-04
pydeseq2 public A python implementation of DESeq2. 2024-09-04
pytrimal public Cython bindings and Python interface to trimAl, a tool for automated alignment trimming. 2024-09-04
last public LAST finds & aligns related regions of sequences. 2024-09-03
spaln public Map and align a set of cDNA/EST or protein sequences onto a genome 2024-09-03
nextstrain-cli public The Nextstrain command-line interface (CLI) 2024-09-03
jvarkit public Java utilities for Bioinformatics. 2024-09-03
mehari public VEP-like tool for sequence ontology and HGVS annotation of VCF files written in Rust. 2024-09-03
distle public Fast distance matrix calculations on fasta and cgmlst files 2024-09-03
galah public Galah aims to be a more scalable metagenome assembled genome (MAG) dereplication method. 2024-09-03
argo public Argo: species-resolved profiling of antibiotic resistant genes with long-read metagenomics 2024-09-03
perl-graph public a Perl extension for keeping data partially sorted 2024-09-02
mgnify-pipelines-toolkit public Collection of scripts and tools for MGnify pipelines 2024-09-02
beav public beav: Bacterial genome and mobile element annotation pipeline 2024-09-02
aviary public End-to-end metagenomics hybrid assembly and binning pipeline. 2024-09-02

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