bioconda / bioconda-utilsLinks
Utilities for building and managing bioconda recipes
☆103Updated last month
Alternatives and similar repositories for bioconda-utils
Users that are interested in bioconda-utils are comparing it to the libraries listed below
Sorting:
- Sequana: a set of Snakemake NGS pipelines☆145Updated last month
- Extension for Jupyter which integrates igv.js☆154Updated 2 years ago
- Simple FASTQ quality assessment using Python☆108Updated 4 years ago
- Testing building mulled containers for multi-requirement tools.☆78Updated this week
- Tools for manipulating biological data, particularly multiple sequence alignments☆158Updated last month
- Documentation and description of AWS iGenomes S3 resource.☆116Updated 9 months ago
- Plugins for the Ensembl Variant Effect Predictor (VEP)☆158Updated 3 weeks ago
- Example Nextflow pipelines and programming techniques☆106Updated 4 months ago
- Demonstrating best practices for bioinformatics command line tools☆116Updated 4 years ago
- ☆63Updated 8 years ago
- A collection of reusable WDL tasks. Category:Other☆88Updated last month
- python access to UCSC genomes database☆136Updated 5 years ago
- Assembly and intrahost/low-frequency variant calling for viral samples☆142Updated last week
- Long read production pipelines☆148Updated this week
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆125Updated 5 years ago
- small RNA analysis from NGS data☆37Updated last year
- An NGS read trimming tool that is specific, sensitive, and speedy. (production)☆122Updated 4 months ago
- Scripts, utilities and programs for genomic bioinformatics.☆83Updated 2 weeks ago
- Galaxy RNA workbench☆40Updated 4 years ago
- Config files used to define parameters specific to compute environments at different Institutions☆103Updated last week
- Nextflow pipeline for analysis of direct RNA Nanopore reads☆106Updated 2 months ago
- Platypus Variant Caller☆108Updated last year
- AdapterRemoval v2 - rapid adapter trimming, identification, and read merging☆113Updated this week
- Very simple, pure python, BAM file reader☆79Updated 6 years ago
- Biopieces is a bioinformatic framework of tools easily used and easily created.☆142Updated 7 years ago
- Fast HLA type inference from whole-genome data☆137Updated 5 months ago
- Test data to be used for automated testing with the nf-core pipelines☆138Updated last week
- PAired-eND Assembler for DNA sequences☆136Updated 4 years ago
- Galaxy Admin Training☆60Updated 9 months ago
- CLI for interacting with Cromwell servers☆55Updated last year