A Nextflow workflow to generate lift over files for any pair of genomes
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Updated
Aug 26, 2026 - Nextflow
A Nextflow workflow to generate lift over files for any pair of genomes
A simple DSL2 workflow: tutorial
Nextflow workflow syntax highlighting and snippets for Sublime Text 4
A repository for hosting Nextflow DSL2 module files containing tool-specific process definitions and their associated documentation for MSKCC
Automatized Polygenic Score Prediction
Nextflow workflow syntax highlighting and snippets for Sublime Text 4
Nextflow DSL2 tRNA and ncRNA fragment identification pipeline for small RNA-seq data
A Nextflow pipeline for integrated small RNA-seq and mRNA-seq analysis to uncover exercise-associated miRNA–mRNA regulatory networks.
This is a personal project focused on creating uniformal pipeline for processing RNA-seq data with the end goal to create a .Rdata object which can be imported into R/Shiny app for downstream analysis and hypothesis testing.
Nextflow DSL2 long-read RNA-seq pipeline: MisER splice correction → IsoQuant → oarfish → swish/fishpond differential expression (DTE/DTU/DGE)
Containerized Nextflow DSL2 workflow for viral intra-host variant calling (iSNV), quasispecies haplotype reconstruction, and evolutionary selection analysis.
Working through NextFlow tutorials. See https://github.com/nextflow-io/training
nextflow pipeline for BGC-QUAST tool
A modular Nextflow DSL2 pipeline implementing the GATK Best Practices for germline variant discovery from FASTQ preprocessing to functional variant annotation using Ensembl VEP.
Reproducible Nextflow DSL2 FASTQ QC pipeline with a hard validation gate - 42 unit tests, CI that verifies the gate fires
A small pipeline to generate genome statistics
Nextflow resequencing pipeline with bwa-mem and freebayes
Identifying allele-specific isoform expression with allspice🧂
Production Nextflow DSL2 germline variant calling pipeline with biomarker reproducibility analysis and AWS execution
A modular Nextflow DSL2 pipeline for reproducible plant de novo genome and transcriptome assembly, quality control, validation, and functional analysis.
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