VarScan2 analysis of de novo variants in monozygotic twins discordant for schizophrenia. (April 2017)
- Record Type:
- Journal Article
- Title:
- VarScan2 analysis of de novo variants in monozygotic twins discordant for schizophrenia. (April 2017)
- Main Title:
- VarScan2 analysis of de novo variants in monozygotic twins discordant for schizophrenia
- Authors:
- Reble, Emma
Castellani, Christina A.
Melka, Melkaye G.
O'Reilly, Richard
Singh, Shiva M. - Abstract:
- Abstract : Objectives: Monozygotic twins with near-identical genotypes and discordance for complex diseases represent an exceptional resource to ascertain disease etiology. This strategy has been particularly effective with the availability of high-resolution complete individual genome sequencing. The challenge is using effective approaches to identify relevant differences that may cause or contribute toward disease discordance. Participants and methods: This study carried out a VarScan2 bioinformatic analysis and a pathway analysis on whole-genome sequences from two sets of monozygotic twins. Results: Variants were identified that were present in the affected twin, but not found in the unaffected twin. Such variations are expected to be de novo and originate during the independent development of the twins and may make them discordant for the disease. The genes and de novo variants identified in this experiment are compatible with their involvement in schizophrenia. Further analysis of the variants identified pathways including glutamate receptor signaling that have been implicated in this neurodevelopmental disease. Conclusion: The results support the polygenic nature of schizophrenia and the threshold model for its development. The results also show the effectiveness of VarScan2 to identify 'the needle in the hay stack' that may cause schizophrenia, specifically in the two patients. It offers a proof of principle for assessment of the genetic etiology of complex disordersAbstract : Objectives: Monozygotic twins with near-identical genotypes and discordance for complex diseases represent an exceptional resource to ascertain disease etiology. This strategy has been particularly effective with the availability of high-resolution complete individual genome sequencing. The challenge is using effective approaches to identify relevant differences that may cause or contribute toward disease discordance. Participants and methods: This study carried out a VarScan2 bioinformatic analysis and a pathway analysis on whole-genome sequences from two sets of monozygotic twins. Results: Variants were identified that were present in the affected twin, but not found in the unaffected twin. Such variations are expected to be de novo and originate during the independent development of the twins and may make them discordant for the disease. The genes and de novo variants identified in this experiment are compatible with their involvement in schizophrenia. Further analysis of the variants identified pathways including glutamate receptor signaling that have been implicated in this neurodevelopmental disease. Conclusion: The results support the polygenic nature of schizophrenia and the threshold model for its development. The results also show the effectiveness of VarScan2 to identify 'the needle in the hay stack' that may cause schizophrenia, specifically in the two patients. It offers a proof of principle for assessment of the genetic etiology of complex disorders where discordance of monozygotic twins is an established phenomenon. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Psychiatric genetics. Volume 27:Number 2(2017:Apr.)
- Journal:
- Psychiatric genetics
- Issue:
- Volume 27:Number 2(2017:Apr.)
- Issue Display:
- Volume 27, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 27
- Issue:
- 2
- Issue Sort Value:
- 2017-0027-0002-0000
- Page Start:
- Page End:
- Publication Date:
- 2017-04
- Subjects:
- bioinformatics -- schizophrenia -- twin study -- whole-genome sequencing
Mental illness -- Genetic aspects -- Periodicals
Periodicals
616.89042 - Journal URLs:
- http://journals.lww.com/psychgenetics/pages/default.aspx ↗
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=toc&D=yrovft&AN=00041444-000000000-00000 ↗
http://journals.lww.com/pages/default.aspx ↗
http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=0955-8829;screen=info;ECOIP ↗ - DOI:
- 10.1097/YPG.0000000000000162 ↗
- Languages:
- English
- ISSNs:
- 0955-8829
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6946.214050
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8052.xml