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bioconda / packages

Package Name Access Summary Updated
phylodm public Efficient calculation of phylogenetic distance matrices. 2024-12-14
python-hppy public An intuitive HyPhy interface for Python 2024-12-14
gargammel-slim public Tool for simulating ancient DNA datasets 2024-12-14
safesim public SafeSeqS variant simulator 2024-12-14
vphaser2 public V-Phaser 2 is a tool to call variants in genetically heterogeneous populations from ultra-deep sequence data 2024-12-14
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. 2024-12-14
telseq public A software for calculating telomere length 2024-12-14
tatajuba public Identification and classification of homopolymeric tracts from reads 2024-12-14
perl-namespace-autoclean public Keep imports out of your namespace 2024-12-14
perl-string-approx public No Summary 2024-12-14
libgab public Several C++ subroutines useful for bioinformatics 2024-12-14
encode-blacklist public The ENCODE Blacklist: Identification of Problematic Regions of the Genome 2024-12-14
fann public No Summary 2024-12-14
fsa public FSA is a probabilistic multiple sequence alignment algorithm which uses a "distance-based" approach to aligning homologous protein, RNA or DNA sequences. 2024-12-14
sracat public a command-line tool for extracting unordered read data from SRA files 2024-12-14
merfin public Improved variant filtering and polishing via k-mer validation. 2024-12-14
r-acidcli public Interative R command line interface toolkit for Acid Genomics packages. 2024-12-14
mammal public Accelerated Estimation of Frequency Classes in Site-heterogeneous Profile Mixture Models 2024-12-14
winnowmap public Winnowmap is a long-read mapping algorithm optimized for mapping ONT and PacBio reads to repetitive reference sequences. 2024-12-14
fastqpuri public fastq quality assessment and filtering tool 2024-12-14
bioawk public BWK awk modified for biological data 2024-12-14
symbiontscreener public Symbiont-Screener is a reference-free approach to identifying high-confidence host's long reads from symbionts and contaminants and overcoming the low sequencing accuracy according to a trio-based screening model. 2024-12-14
ucsc-genepredhisto public get data for generating histograms from a genePred file. 2024-12-14
rna-seqc public Fast, efficient RNA-Seq metrics for quality control and process optimization. 2024-12-14
moni public A Pangenomics Index for Finding MEMs 2024-12-14
modeltest-ng public ModelTest-NG is a tool for selecting the best-fit model of evolution for DNA and protein alignments. 2024-12-14
genform public Generation of molecular formulas by high-resolution MS and MS/MS data 2024-12-14
bicseq2-seg public BICseq2-seg is for detecting CNVs based on the normalized data given by BICseq2-norm. 2024-12-14
ucsc-splitfilebycolumn public Split text input into files named by column value 2024-12-14
phylocsfpp public A fast and user-friendly implementation of PhyloCSF with annotation tools. 2024-12-14
pretextmap public Paired REad TEXTure Mapper. Converts SAM formatted read pairs into genome contact maps. 2024-12-14
r-saige public SAIGE is an R package with Scalable and Accurate Implementation of Generalized mixed model (Chen, H. et al. 2016) 2024-12-14
stringdecomposer public A tool for decomposing of strings into a set of given monomers 2024-12-14
ucsc-axttomaf public Convert from axt to maf format 2024-12-14
ucsc-coltransform public Add and/or multiply column by constant. 2024-12-14
boms public Cell Segmentation for Spatial Transcriptomics Data using BOMS 2024-12-14
illumina-interop public The Illumina InterOp libraries are a set of common routines used for reading and writing InterOp metric files. These metric files are binary files produced during a run providing detailed statistics about a run. In a few cases, the metric files are produced after a run during secondary analysis (index metrics) or for faster display of a subset of the original data (collapsed quality scores). 2024-12-14
shark public Mapping-free filtering of useless RNA-Seq reads 2024-12-14
akt public Ancestry and Kinship Tools (AKT) 2024-12-14
reads2graph public reads2graph is an efficient tool for constructing edit-distance-based read graph from short-read sequencing data. 2024-12-14
dashing public Fast and accurate genomic distances using HyperLogLog 2024-12-14
reseq public ReSeq Illumina/BGI simulator 2024-12-14
ucsc-mafaddirows public add 'i' rows to a maf 2024-12-14
zorro public ZORRO is a probabilistic masking program that assigns confidence scores to each column in a multiple sequence alignment. 2024-12-14
libgtextutils public No Summary 2024-12-14
coatran public Coalescent tree simulation along a transmission network 2024-12-14
ucsc-maforder public order components within a maf file 2024-12-14
maast public Microbial agile accurate SNP Typer 2024-12-14
sciphi public Single-cell mutation identification via phylogenetic inference 2024-12-14
r-cleangeostreamr public Automatic curation of spatially annotated data. 2024-12-14

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