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bioconda / packages

Package Name Access Summary Updated
quicksect public A cythonized, extended version of the interval search tree in bx 2024-08-02
filtlong public Filtlong is a tool for filtering long reads. It can take a set of long reads and produce a smaller, better subset. It uses both read length (longer is better) and read identity (higher is better) when choosing which reads pass the filter. 2024-08-01
r-ichorcna public Estimating tumor fraction in cell-free DNA from ultra-low-pass whole genome sequencing. 2024-08-01
nextflow public A DSL for data-driven computational pipelines http://nextflow.io 2024-08-01
sequencetools public Tools for population genetics on sequencing data 2024-08-01
sourmash public Compute and compare MinHash signatures for DNA data sets. 2024-08-01
rnashapes public RNAshape abstraction maps structures to a tree-like domain of shapes, retaining adjacency and nesting of structural features, but disregarding helix lengths. Shape abstraction integrates well with dynamic programming algorithms, and hence it can be applied during structure prediction rather than afterwards. This avoids exponential explosion and can still give us a non-heuristic and complete account of properties of the molecule's folding space. 2024-07-31
perl-datetime-locale public Localization support for DateTime.pm 2024-07-31
perl-json public JSON (JavaScript Object Notation) encoder/decoder 2024-07-31
perl-json-xs public JSON serialising/deserialising, done correctly and fast 2024-07-31
ntcard public Estimating k-mer coverage histogram of genomics data 2024-07-25
links public Long Interval Nucleotide K-mer Scaffolder 2024-07-25
morpheus public mass spectrometry–based proteomics database search algorithm 2024-07-25
seqtk public Seqtk is a fast and lightweight tool for processing sequences in the FASTA or FASTQ format 2024-07-24
entrez-direct public Entrez Direct (EDirect) is an advanced method for accessing the NCBI's set of interconnected databases (publication, sequence, structure, gene, variation, expression, etc.) from a UNIX terminal window. Functions take search terms from command-line arguments. Individual operations are combined to build multi-step queries. Record retrieval and formatting normally complete the process. 2024-07-23
kma public KMA is mapping a method designed to map raw reads directly against redundant databases, in an ultra-fast manner using seed and extend. 2024-07-23
bracken public Bracken (Bayesian Reestimation of Abundance with KrakEN) is a highly accurate statistical method that computes the abundance of species in DNA sequences from a metagenomics sample. 2024-07-22
pydna public Representing double stranded DNA and functions for simulating cloning and homologous recombination between DNA molecules. 2024-07-19
pybedtools public Wraps BEDTools for use in Python and adds many additional features. 2024-07-19
nonpareil public Estimate average coverage and create curves for metagenomic datasets 2024-07-19
r-ic10 public Implementation of the classifier described in the paper 'Genome-driven integrated classification of breast cancer validated in over 7,500 samples' (Ali HR et al., Genome Biology 2014). It uses copy number and/or expression form breast cancer data, trains a pamr classifier (Tibshirani et al.) with the features available and predicts the iC10 group. 2024-07-19
primer3-py public Python bindings for Primer3 2024-07-19
gffcompare public GffCompare by Geo Pertea 2024-07-18
viennarna public ViennaRNA package -- RNA secondary structure prediction and comparison 2024-07-18
fido public No Summary 2024-07-17
cancerit-allelecount public Support code for NGS copy number algorithms 2024-07-17
bowtie public An ultrafast memory-efficient short read aligner 2024-07-17
bwa public The BWA read mapper. 2024-07-17
fgbio public A set of tools for working with genomic and high throughput sequencing data, including UMIs 2024-07-16
fastp public A ultra-fast FASTQ preprocessor with full features (QC/adapters/trimming/filtering/splitting...) 2024-07-16
libbigwig public A C library for handling bigWig files 2024-07-16
graftm public GraftM is a pipeline used for identifying and classifying marker gene reads from metagenomic datasets 2024-07-16
mappy public Minimap2 Python binding 2024-07-15
bellmans-gapc public A language and compiler for algebraic dynamic programming. 2024-07-15
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). 2024-07-15
dropseq_tools public Package for the analysis of Drop-seq data developed by Jim Nemesh in the McCarroll Lab 2024-07-15
r-rrbgen public A lightweight limited functionality R bgen read/write library 2024-07-15
pairix public 2D indexing on bgzipped text files of paired genomic coordinates 2024-07-12
perl-digest-sha1 public Perl interface to the SHA-1 algorithm 2024-07-12
breseq public A computational pipeline for finding mutations relative to a reference sequence in short-read DNA re-sequencing data. 2024-07-12
skesa public Strategic Kmer Extension for Scrupulous Assemblies & Sequence Assembly Using Target Enrichment 2024-07-12
gap2seq public Gap2Seq is a tool for filling gaps between contigs in genome assemblies. 2024-07-12
vcftools public A set of tools written in Perl and C++ for working with VCF files. This package only contains the C++ libraries whereas the package perl-vcftools-vcf contains the perl libraries 2024-07-11
taxonkit public A Cross-platform and Efficient NCBI Taxonomy Toolkit 2024-07-11
raxml public Phylogenetics - Randomized Axelerated Maximum Likelihood. 2024-07-11
xtandem public No Summary 2024-07-11
csvtk public A cross-platform, efficient, practical CSV/TSV toolkit 2024-07-11
seqkit public a cross-platform and ultrafast toolkit for FASTA/Q file manipulation 2024-07-11
mmseqs2 public MMseqs2: ultra fast and sensitive sequence search and clustering suite 2024-07-11
kalign2 public Kalign is a fast and accurate multiple sequence alignment algorithm designed to align large numbers of protein sequences. 2024-07-11

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