SIQ: easy quantitative measurement of mutation profiles in sequencing data
Abstract
Establishing mutational outcomes after genome editing is of increasing importance with the advent of highly efficient genome-targeting tools. Next-generation sequencing (NGS) has become a vital method to investigate the extent of mutagenesis at specific target sites. Thus, robust and simple-to-use software that enables researchers to retrieve mutation profiles from NGS data is needed. Here, we present Sequence Interrogation and Quantification (SIQ), a tool that can analyse sequence data of any targeted experiment (e.g. CRISPR, I-SceI, TALENs) with a focus on event classification such as deletions, single-nucleotide variations, (templated) insertions and tandem duplications. SIQ results can be directly analysed and visualized via SIQPlotteR, an interactive web tool that we made freely available. Using novel and insightful tornado plot visualizations as outputs we illustrate that SIQ readily identifies differences in mutational signatures obtained from various DNA-repair deficient genetic backgrounds. SIQ greatly facilitates the interpretation of complex sequence data by establishing mutational profiles at specific loci and is, to our knowledge, the first tool that can analyse Sanger sequence data as well as short and long-read NGS data (e.g. Illumina and PacBio).
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 33
- FWCI
- 2.04
- Field percentile
- top 12%
- 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
- SomaticSiMu: a mutational signature simulator
David J. Chen, Gurjit S. Randhawa, … Kathleen Allen Hill·BioinformaticsPeer-reviewed·Mar 4, 2022
- Mutation Reporter: Protein-Level Identification of Single and Compound Mutations in NGS Data
Mikaela Teodoro, Rosana V. das Chagas, … João Meidânis·bioRxiv·May 30, 2024
- 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
- EdiTyper: a high-throughput tool for analysis of targeted sequencing data from genome editing experiments
Alexandre Yahi, Paul Hoffman, … Tuuli Lappalainen·bioRxiv·Jul 30, 2020
- Boquila: NGS read simulator to eliminate read nucleotide bias in sequence analysis
Ümit Akköse, Ogün Adebalı·TURKISH JOURNAL OF BIOLOGYPeer-reviewed·Jan 1, 2023
- Web-based design and analysis tools for CRISPR base editing
Gue‐Ho Hwang, Jeongbin Park, … Sangsu Bae·BMC BioinformaticsPeer-reviewed·Dec 1, 2018