There are 5 repositories under snakemake-pipeline topic.
A flexible, scalable, and reproducible pipeline to automate variant calling from sequence reads.
A Snakemake workflow to process single samples or cohorts of Illumina paired-end sequencing data (WGS or WES) using trim galore/bwa/GATK4/parabricks.
Snakemake workflow for scoring and comparing multiple bacterial genome assemblies (Illumina, Nanopore) to reference genome(s)
Snakemake workflow for bacterial genome assembly + polishing for Oxford Nanopore (ONT) sequencing using multiple tools
A comprehensive quality-control and quantification RNA-seq pipeline
Project for apaQTL MS. The workflowr project apaQTL by brimittleman
A Snakemake workflow to filter, annotate and prepare variant call format (VCF) data for scout using GATK4, SnpSift, VEP and genmod. Designed to be used after human_genomics_pipeline.
Simple template for running snakemake with R
Software for RNA-Seq analysis to create sample-specific proteoform databases from RNA-Seq data
A snakemake workflow to perform Alternative Splicing analysis from RNA-Seq with SUPPA2.
population structural variant calling with smoove
Snakemake pipeline for analysis and normalization of Hi-C data starting from fastq.gz files. It includes the possibility to perform grouped analyses, TAD, loops and stripes detections, as well as differential compartment and chromatin interaction analyses.
A small snakemake pipeline to perform quality analysis of RNA-Seq data with FastQC.
Template directory for creating a snakemake pipeline
Short read mapping and variant calling
🪆🦖 A snakemake wrapper around Nesvilab's FragPipe-CLI. In a perfect world, this pipeline was based on Sage.
bacterial strain identification
This repo contains scripts and workflows for performing bulk transcriptomics analyses
A repository for RNA-seq workflow
Final project submission for IS477 course at University of Illinois Urbana-Champaign. Utilized Snakemake for efficient creation of research objects, applying semester's knowledge on data curation, management, and reproducibility.
ChIPseq pipeline for Pasini's lab written in snakemake
CutNtag pipeline for Pasini's lab written in snakemake
RNAseq pipeline for Pasini's lab written in snakemake
Pipeline to map short reads from several samples to a reference genome
Pipeline for analyses of multiple pathogens, like SARS-CoV-2 with positivity rate analyses
Simple Snakemake RNA-Seq pipeline
pipeline to perform gbs and genetic fitness analysis
Hi-C processing pipeline in snakemake.
utility for writing the snakemake files with faster iterations.
Python & R multi-language data analysis pipeline
Work at NIST: snakemake workflow to get short tandem repeats from WGS GIAB samples. R script for downstream processing and concordance