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Package Name Access Summary Updated
r-seurat-data public Single cell RNA sequencing datasets can be large, consisting of matrices that contain expression data for several thousand features across several thousand cells. This package is designed to easily install, manage, and learn about various single-cell datasets, provided Seurat objects and distributed as independent packages. 2024-12-14
quicktree public Fast implementation of the neighbour-joining phylogenetic inference method 2024-12-14
ucsc-qactoqa public convert from compressed to uncompressed 2024-12-14
ropebwt2 public Incremental construction of FM-index for DNA sequences 2024-12-14
enano public ENANO is a FASTQ compression tool especially designed for nanopore sequencing FASTQ files. 2024-12-14
seqfu public DNA sequence utilities 2024-12-14
newick_utils public The Newick Utilities are a suite of Unix shell tools for processing phylogenetic trees. We distribute the package under the BSD License. Functions include re-rooting, extracting subtrees, trimming, pruning, condensing, drawing (ASCII graphics or SVG). 2024-12-14
sgdemux public Tool for demultiplexing sequencing data generated on Singular Genomics' sequencing instruments. 2024-12-14
mapad public An aDNA aware short-read mapper 2024-12-14
skani public skani is a fast and robust tool for calculating ANI between metagenome assembled genomes and contigs. 2024-12-14
mapping-iterative-assembler public Consensus calling or `reference assisted assembly`, chiefly of ancient mitochondria. 2024-12-14
r-intego public An unsupervised gene clustering algorithm based on the integration of external biological knowledge, such as Gene Ontology annotations, into expression data. 2024-12-14
htslib public C library for high-throughput sequencing data formats. 2024-12-14
bbknn public Batch balanced KNN 2024-12-14
ucsc-genepredtoprot public create protein sequences by translating gene annotations 2024-12-14
wgsim public No Summary 2024-12-14
deepchopper-cli public A CLI for Genomic Language Model for Chimera Artifact Detection in Nanopore Direct RNA Sequencing. 2024-12-14
atac public No Summary 2024-12-14
table2asn public table2asn is a command-line program that creates sequence records for submission to GenBank - replaces tbl2asn. 2024-12-14
slow5tools public Toolkit for S/bLOW5 format 2024-12-14
ucsc-bedpileups public Find (exact) overlaps if any in bed input 2024-12-14
cansam public C++ binding for SAM/BAM files 2024-12-14
perl-time-hires public High resolution alarm, sleep, gettimeofday, interval timers 2024-12-14
bowtie public An ultrafast memory-efficient short read aligner 2024-12-14
perl-digest-sha1 public Perl interface to the SHA-1 algorithm 2024-12-14
ucsc-fatrans public Translate DNA .fa file to peptide 2024-12-14
contrafold public CONditional TRAining for RNA Secondary Structure Prediction 2024-12-14
ucsc-checkagpandfa public takes a .agp file and .fa file and ensures that they are in synch 2024-12-14
perl-unicode-normalize public Unicode Normalization Forms 2024-12-14
ucsc-mafmefirst public Move component to top if it is one of the named ones. 2024-12-14
meta-neuro public Medial Tractography Analysis (MeTA) 2024-12-14
fasttree public FastTree infers approximately-maximum-likelihood phylogenetic trees from alignments of nucleotide or protein sequences 2024-12-14
ucsc-chainantirepeat public Get rid of chains that are primarily the results of repeats and degenerate DNA 2024-12-14
crass public Crass (The CRISPR Assembler) is a program that searches through raw metagenomic reads for Clustered Regularly Interspersed Short Palindromic Repeats 2024-12-14
ucsc-hgsqldump public Execute mysqldump using passwords from .hg.conf 2024-12-14
perl-unicode-map public Map charsets from and to UTF-16 unicode 2024-12-14
ucsc-mafspecieslist public Scan maf and output all species used in it. 2024-12-14
ucsc-pslrc public reverse-complement psl 2024-12-14
meraculous public Meraculous is a whole genome assembler for Next Generation Sequencing data, geared for large genomes. It's hybrid k-mer/read-based approach capitalizes on the high accuracy of Illumina sequence by eschewing an explicit error correction step which we argue to be redundant with the assembly process. Meraculous achieves high performance with large datasets by utilizing lightweight data structures and multi-threaded parallelization, allowing to assemble human-sized genomes on a high-cpu cluster in under a day. The process pipeline implements a highly transparent and portable model of job control and monitoring where different assembly stages can be executed and re-executed separately or in unison on a wide variety of architectures. 2024-12-14
hisat2 public Graph-based alignment of next generation sequencing reads to a population of genomes. 2024-12-14
ucsc-bedgraphpack public Pack together adjacent records representing same value. 2024-12-14
perl-convert-binary-c public Binary Data Conversion using C Types 2024-12-14
sketchy public Real-time lineage hashing and genotyping of bacterial pathogens 2024-12-14
parafly public Given a file containing a list of unix commands, multithreading is used to process the commands in parallel on a single server. Success/failure is captured, and failed commands are retained and reported. 2024-12-14
phyml public Phylogenetic estimation using (Maximum) Likelihood 2024-12-14
ucsc-maftoaxt public Convert from maf to axt format 2024-12-14
irfinder public Intron Retention Finder 2024-12-14
ucsc-genepredtobed public Convert from genePred to bed format. Does not yet handle genePredExt 2024-12-14
tntblast public Searching DNA/RNA sequence databases with PCR and/or probe queries 2024-12-14
ucsc-chaincleaner public Remove chain-breaking alignments from chains that break nested chains. 2024-12-14

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