Related Experiment Video
Updated: Jun 9, 2026

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
Published on: October 18, 2013
gyōza: a Snakemake workflow for modular analysis of deep-mutational scanning data.
Romain Durand1,2,3,4, Alicia Pageau1,2,3,4, Christian R Landry1,2,3,4
1Département de Biochimie, de Microbiologie et de Bio-Informatique, Faculté des Sciences et de Génie, Université Laval, Québec (QC), G1V 0A6, Canada.
We developed gyōza, a user-friendly workflow for analyzing deep-mutational scanning (DMS) data. This tool simplifies the process from raw sequencing to functional impact scores, aiding protein engineering and drug discovery research.
Area of Science:
- Molecular Biology
- Bioinformatics
- Protein Engineering
Background:
- Deep-mutational scanning (DMS) is a high-throughput method for analyzing protein variants.
- Existing DMS analysis methods can be complex and require significant programming expertise.
- There is a need for accessible tools to interpret large-scale DMS datasets.
Purpose of the Study:
- To introduce gyōza, a Snakemake-based workflow for analyzing DMS data.
- To provide a user-friendly pipeline requiring minimal programming knowledge.
- To facilitate the interpretation of DMS experiments, including time-series analyses.
Main Methods:
- Developed a Snakemake workflow named gyōza.
- Integrated quality control measures.
- Automated the generation of HTML reports for data visualization.
Main Results:
- gyōza processes raw sequencing data into functional impact scores.
- The workflow includes comprehensive documentation for ease of use.
- The pipeline is designed for efficient analysis of time-series DMS experiments.
Conclusions:
- gyōza simplifies and standardizes DMS data analysis.
- The tool lowers the barrier to entry for researchers using DMS.
- gyōza is expected to accelerate discoveries in protein science and related fields.
More Related Videos
06:59Using Next Generation Sequencing to Identify Mutations Associated with Repair of a CAS9-induced Double Strand Break Near the CD4 Promoter
Published on: March 31, 2022
10:47Author Spotlight: High-Throughput Image-Based Quantification of Mitochondrial DNA Synthesis and Distribution
Published on: May 5, 2023