An integrative framework for the identification of double minute chromosomes using next generation sequencing data. Issue 2 (December 2015)
- Record Type:
- Journal Article
- Title:
- An integrative framework for the identification of double minute chromosomes using next generation sequencing data. Issue 2 (December 2015)
- Main Title:
- An integrative framework for the identification of double minute chromosomes using next generation sequencing data
- Authors:
- Hayes, Matthew
Li, Jing - Abstract:
- Abstract Background Double minute chromosomes are circular fragments of DNA whose presence is associated with the onset of certain cancers. Double minutes are lethal, as they are highly amplified and typically contain oncogenes. Locating double minutes can supplement the process of cancer diagnosis, and it can help to identify therapeutic targets. However, there is currently a dearth of computational methods available to identify double minutes. We propose a computational framework for the idenfication of double minute chromosomes using next-generation sequencing data. Our framework integrates predictions from algorithms that detect DNA copy number variants, and it also integrates predictions from algorithms that locate genomic structural variants. This information is used by a graph-based algorithm to predict the presence of double minute chromosomes. Results Using a previously published copy number variant algorithm and two structural variation prediction algorithms, we implemented our framework and tested it on a dataset consisting of simulated double minute chromosomes. Our approach uncovered double minutes with high accuracy, demonstrating its plausibility. Conclusions Although we only tested the framework with three programs (RDXplorer, BreakDancer, Delly), it can be extended to incorporate results from programs that 1) detect amplified copy number and from programs that 2) detect genomic structural variants like deletions, translocations, inversions, and tandemAbstract Background Double minute chromosomes are circular fragments of DNA whose presence is associated with the onset of certain cancers. Double minutes are lethal, as they are highly amplified and typically contain oncogenes. Locating double minutes can supplement the process of cancer diagnosis, and it can help to identify therapeutic targets. However, there is currently a dearth of computational methods available to identify double minutes. We propose a computational framework for the idenfication of double minute chromosomes using next-generation sequencing data. Our framework integrates predictions from algorithms that detect DNA copy number variants, and it also integrates predictions from algorithms that locate genomic structural variants. This information is used by a graph-based algorithm to predict the presence of double minute chromosomes. Results Using a previously published copy number variant algorithm and two structural variation prediction algorithms, we implemented our framework and tested it on a dataset consisting of simulated double minute chromosomes. Our approach uncovered double minutes with high accuracy, demonstrating its plausibility. Conclusions Although we only tested the framework with three programs (RDXplorer, BreakDancer, Delly), it can be extended to incorporate results from programs that 1) detect amplified copy number and from programs that 2) detect genomic structural variants like deletions, translocations, inversions, and tandem repeats. The software that implements the framework can be accessed here:https://github.com/mhayes20/DMFinder … (more)
- Is Part Of:
- BMC genetics. Volume 16:Issue 2(2015)
- Journal:
- BMC genetics
- Issue:
- Volume 16:Issue 2(2015)
- Issue Display:
- Volume 16, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 16
- Issue:
- 2
- Issue Sort Value:
- 2015-0016-0002-0000
- Page Start:
- 1
- Page End:
- 7
- Publication Date:
- 2015-12
- Subjects:
- amplicon -- double minute -- next generation sequencing
Genetics -- Periodicals
576.505 - Journal URLs:
- http://www.biomedcentral.com/bmcgenet/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=31 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/1471-2156-16-S2-S1 ↗
- Languages:
- English
- ISSNs:
- 1471-2156
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9996.xml