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bioconda / packages

Package Name Access Summary Updated
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
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
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
ucsc-genepredtoprot public create protein sequences by translating gene annotations 2024-12-14
wgsim public No Summary 2024-12-14
atac public No Summary 2024-12-14
ucsc-bedpileups public Find (exact) overlaps if any in bed input 2024-12-14
py2bit public A package for accessing 2bit files using lib2bit 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
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
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
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
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
ucsc-chaintopslbasic public Basic conversion chain file to psl format 2024-12-14
structure public The program structure is a free software package for using multi-locus genotype data to investigate population structure. Its uses include inferring the presence of distinct populations, assigning individuals to populations, studying hybrid zones, identifying migrants and admixed individuals, and estimating population allele frequencies in situations where many individuals are migrants or admixed. It can be applied to most of the commonly-used genetic markers, including SNPS, microsatellites, RFLPs and AFLPs. 2024-12-14
sfs_code public This article introduces a new forward population genetic simulation program that can efficiently generate samples from populations with complex demographic histories under various models of natural selection. The program (SFS_CODE) is highly flexible, allowing the user to simulate realistic genomic regions with several loci evolving according to a variety of mutation models (from simple to context-dependent), and allows for insertions and deletions. Each locus can be annotated as either coding or non-coding, sex-linked or autosomal, selected or neutral, and have an arbitrary linkage structure (from completely linked to independent). © The Author 2008. Published by Oxford University Press. All rights reserved. 2024-12-13
r-chbutils public Useful utility functions used at the Harvard Chan School Bioinformatics core 2024-12-13
deploid public A software that deconvolutes mixed genomes with unknown proportions. 2024-12-13
ucsc-bigwigcorrelate public Correlate bigWig files, optionally only on target regions. 2024-12-13
ucsc-ticktodate public Convert seconds since 1970 to time and date 2024-12-13
kaiju public Fast and sensitive taxonomic classification for metagenomics 2024-12-13
r-rubic public No Summary 2024-12-13
smhasher public No Summary 2024-12-13
ucsc-chromgraphtobin public Make binary version of chromGraph. 2024-12-13
ucsc-chainprenet public Remove chains that don't have a chance of being netted 2024-12-13
zerone public Zerone discretizes several ChIP-seq replicates simultaneously and resolves conflicts between them. 2024-12-13
perl-math-cdf public Generate probabilities and quantiles from several statistical probability functions 2024-12-13
ngmlr public ngmlr is a long-read mapper designed to align PacBio or Oxford Nanopore reads to a reference genome and optimized for structural variation detection 2024-12-13
takeabreak public tool that can detect inversion breakpoints directly from raw NGS reads, without the need of any reference genome and without de novo assembling the genomes 2024-12-13

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