Mutation Reporter: Protein-Level Identification of Single and Compound Mutations in NGS Data
Mikaela TeodoroiD, Rosana V. das Chagas, José Andrés YunesiD, Natacha Azussa MigitaiD, João MeidânisiD
Abstract
SummaryNext-generation sequencing (NGS) has accelerated precision medicine by enabling simultaneous analysis of multiple genes and detection of low-frequency mutations. However, few open-source tools allow non-specialized users to transparently adjust quality parameters during mutation analysis. Mutation Reporter was developed to identify both single and compound amino acid alterations directly from raw fastq files of sequencing originated from RNA or exon sequences. The software provides full parameter control--including alignment e-value, minimum read length, minimum read depth, and minimum variant allele frequency (VAF). Availability and implementationMutation Reporter is available to users through a free GNU software license and can be accessed on GitHub (https://github.com/meidanis-lab/mutation-reporter) and as a Code Ocean capsule (https://codeocean.com/capsule/0121109/tree).
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Needlestack: an ultra-sensitive variant caller for multi-sample next generation sequencing data
Tiffany Myriam Delhomme, Patrice Hodonou Avogbe, … Matthieu Foll·NAR Genomics and BioinformaticsPeer-reviewed·Apr 20, 2020
- SIQ: easy quantitative measurement of mutation profiles in sequencing data
Robin van Schendel, Joost Schimmel, Marcel Tijsterman·NAR Genomics and BioinformaticsPeer-reviewed·Jul 9, 2022
- SeqPanther: Sequence manipulation and mutation statistics toolset
James Emmanuel San, Stephanie van Wyk, … Anmol M Kiran·The Journal of Open Source SoftwarePeer-reviewed·Jul 20, 2023
- Target variant detection in leukemia using unaligned RNA-Seq reads
Eric Olivier Audemard, Patrick Gendron, … Sébastien Lemieux·bioRxiv·Apr 17, 2018
- SafeMut: UMI-aware variant simulator incorporating allele-fraction overdispersion in read editing
Xiaofei Zhao, Jingyu Guo, Sizhen Wang·Informatics in Medicine UnlockedPeer-reviewed·Jan 1, 2023
- False Negatives Are a Significant Feature of Next Generation Sequencing Callsets
Dean Bobo, Mikhail Lipatov, … Brenna M. Henn·bioRxiv·Oct 18, 2016