RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing
RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing
About this item
Full title
Author / Creator
Publisher
SAGE Publishing
Journal title
Language
English
Formats
Publication information
Publisher
SAGE Publishing
More information
Scope and Contents
Contents
With rapid advances in DNA sequencing technologies, whole exome sequencing (WES) has become a popular approach for detecting somatic mutations in oncology studies. The initial intent of WES was to characterize single nucleotide variants, but it was observed that the number of sequencing reads that mapped to a genomic region correlated with the DNA...
Alternative Titles
Full title
RefCNV: Identification of Gene-Based Copy Number Variants Using Whole Exome Sequencing
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_b9275063eada4994baf1a3c9055a31d2
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_b9275063eada4994baf1a3c9055a31d2
Other Identifiers
E-ISSN
1176-9351
DOI
10.4137/CIN.S36612
