Aggregate results from bioinformatics analyses across many samples into a single report.
-
Updated
Oct 9, 2024 - JavaScript
Aggregate results from bioinformatics analyses across many samples into a single report.
Structural variation caller using third generation sequencing
A flexible pipeline for complete analysis of bacterial genomes
Toolset for SV simulation, comparison and filtering
🔬 Bioinformatics Notebook. Scripts for bioinformatics pipelines, with quick start guides for programs and video demonstrations.
NGMLR is a long-read mapper designed to align PacBio or Oxford Nanopore (standard and ultra-long) to a reference genome with a focus on reads that span structural variations
Reproducible bioinformatics pipelines in python. Import any Unix tool/command in python.
BioContainers Documentation.
Recommendations to contenarized your bioinformatics software
🚀 seqfu - Sequece Fastx Utilities
Cython bindings and Python interface to Prodigal, an ORF finder for genomes and metagenomes. Now with SIMD!
A quick overview of how to use Bioconda, and create recipes
Data analysis related to the bioconda paper
Analysis of mutations at codon 625 of SF3B1 gene in uveal melanoma
Build a Reproducible Jupyter Workflow From Scratch (2017 NIH Hour of Code)
Add a description, image, and links to the bioconda topic page so that developers can more easily learn about it.
To associate your repository with the bioconda topic, visit your repo's landing page and select "manage topics."