Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles. Issue 19 (23rd May 2017)
- Record Type:
- Journal Article
- Title:
- Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles. Issue 19 (23rd May 2017)
- Main Title:
- Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles
- Authors:
- Bolli, Niccolo
Barcella, Matteo
Salvi, Erika
D'Avila, Francesca
Vendramin, Antonio
De Philippis, Chiara
Munshi, Nikhil C.
Avet‐Loiseau, Herve
Campbell, Peter J.
Mussetti, Alberto
Carniti, Cristiana
Maura, Francesco
Barlassina, Cristina
Corradini, Paolo
Montefusco, Vittorio - Abstract:
- Abstract : BACKGROUND: The authors describe a family with a high penetrance of plasma cell dyscrasias, suggesting inheritance of an autosomal dominant risk allele. METHODS: The authors performed whole‐exome sequencing and reported on a combined approach aimed at the identification of causative variants and risk loci, using the wealth of data provided by this approach. RESULTS: The authors identified gene mutations and single‐nucleotide polymorphisms of potential significance, and pinpointed a known risk locus for myeloma as a potential area of transmissible risk in the family. CONCLUSIONS: To the authors' knowledge, the current study is the first to provide a whole‐exome sequencing approach to such cases, and a framework analysis that could be applied to further understanding of the inherited risk of developing plasma cell dyscrasias. Cancer 2017;123:3701–3708. © 2017 American Cancer Society Abstract : The current study describes a framework analysis of germline next‐generation sequencing data that has the potential to identify the genetic basis of a hereditary predisposition toward cancer in a family. Furthermore, the analysis can provide a solid basis for counseling other members of the family.
- Is Part Of:
- Cancer. Volume 123:Issue 19(2017)
- Journal:
- Cancer
- Issue:
- Volume 123:Issue 19(2017)
- Issue Display:
- Volume 123, Issue 19 (2017)
- Year:
- 2017
- Volume:
- 123
- Issue:
- 19
- Issue Sort Value:
- 2017-0123-0019-0000
- Page Start:
- 3701
- Page End:
- 3708
- Publication Date:
- 2017-05-23
- Subjects:
- gene mutations -- hereditary cancer -- multiple myeloma -- next‐generation sequencing -- single‐nucleotide polymorphism
Cancer -- Periodicals
Cancer -- Cytopathology -- Periodicals
616.99405 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0142 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cncr.30777 ↗
- Languages:
- English
- ISSNs:
- 0008-543X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3046.450000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8794.xml