CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing. Issue 11 (18th November 2021)
- Record Type:
- Journal Article
- Title:
- CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing. Issue 11 (18th November 2021)
- Main Title:
- CNVpytor: a tool for copy number variation detection and analysis from read depth and allele imbalance in whole-genome sequencing
- Authors:
- Suvakov, Milovan
Panda, Arijit
Diesh, Colin
Holmes, Ian
Abyzov, Alexej - Abstract:
- Abstract: Background: Detecting copy number variations (CNVs) and copy number alterations (CNAs) based on whole-genome sequencing data is important for personalized genomics and treatment. CNVnator is one of the most popular tools for CNV/CNA discovery and analysis based on read depth. Findings: Herein, we present an extension of CNVnator developed in Python—CNVpytor. CNVpytor inherits the reimplemented core engine of its predecessor and extends visualization, modularization, performance, and functionality. Additionally, CNVpytor uses B-allele frequency likelihood information from single-nucleotide polymorphisms and small indels data as additional evidence for CNVs/CNAs and as primary information for copy number–neutral losses of heterozygosity. Conclusions: CNVpytor is significantly faster than CNVnator—particularly for parsing alignment files (2–20 times faster)—and has (20–50 times) smaller intermediate files. CNV calls can be filtered using several criteria, annotated, and merged over multiple samples. Modular architecture allows it to be used in shared and cloud environments such as Google Colab and Jupyter notebook. Data can be exported into JBrowse, while a lightweight plugin version of CNVpytor for JBrowse enables nearly instant and GUI-assisted analysis of CNVs by any user. CNVpytor release and the source code are available on GitHub at https://github.com/abyzovlab/CNVpytor under the MIT license.
- Is Part Of:
- GigaScience. Volume 10:Issue 11(2021)
- Journal:
- GigaScience
- Issue:
- Volume 10:Issue 11(2021)
- Issue Display:
- Volume 10, Issue 11 (2021)
- Year:
- 2021
- Volume:
- 10
- Issue:
- 11
- Issue Sort Value:
- 2021-0010-0011-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-11-18
- Subjects:
- copy number variations -- copy number alternations -- whole-genome sequencing -- Python
Information storage and retrieval systems -- Research -- Periodicals
Biology -- Research -- Periodicals
Medical sciences -- Research -- Periodicals
Database management -- Periodicals
570.285 - Journal URLs:
- http://www.gigasciencejournal.com/ ↗
http://www.oxfordjournals.org/ ↗ - DOI:
- 10.1093/gigascience/giab074 ↗
- Languages:
- English
- ISSNs:
- 2047-217X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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