There are 66 repositories under bioinformatics-pipeline topic.
Compute over Data framework for public, transparent, and optionally verifiable computation
Rapid large-scale prokaryote pan genome analysis
Whole Genome Sequencing analysis, WGS analysis
Artemis is a free genome viewer and annotation tool that allows visualization of sequence features and the results of analyses within the context of the sequence, and its six-frame translation
Finds SNP sites from a multi-FASTA alignment file
GCP for Bioinformatics Researchers
A tool to circularize genome assemblies
ATAC-seq and DNase-seq processing pipeline
Antimicrobial Resistance Identification By Assembly
Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins
Automated and customizable preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workflows. Works equally easy with public as local data.
NGLess: NGS with less work
RNA sequencing analysis software
A handy variant calling pipeline generator for whole-genome sequencing (WGS) and whole exom sequencing data (WES) analysis. 一个简易且全面的 WGS/WES 分析流程生成器.
A modular annotation tool for genomic variants
An open RNA-Seq data analysis pipeline tutorial with an example of reprocessing data from a recent Zika virus study
Cluster single cells and analyze cell clade relationships with colorful visualizations.
AltAnalyze is a multi-functional and easy-to-use software package for automated single-cell and bulk gene and splicing analyses. Easy-to-use precompiled graphical user-interface versions available from our website.
Infectious Disease Sequencing Platform
Plugin for PyCharm / IntelliJ IDEA Platform IDEs which adds support for Snakemake language.
Structural Bioinformatics is awesome. Throw your textbook in the garbage, light the garbage can on fire, and blend the ashes into your cold brew almond milk latte and read this.
Improve the quality of a denovo assembly by scaffolding and gap filling
de novo virus assembler of Illumina paired reads
A fully automated gene annotator from RNA-Seq expression data