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Assessing the utility of confirmatory studies following identification of large-scale genomic imbalances by microarray
Author(s) -
Jennifer N. Sanmann,
Diane L. Pickering,
Denae M. Golden,
Jadd M. Stevens,
Thomas Hempel,
Pamela A. Althof,
Michele L. Wiggins,
Lois J. Starr,
Bhavana J. Davé,
Warren G. Sanger
Publication year - 2015
Publication title -
genetics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1038/gim.2014.204
Subject(s) - microarray , microarray analysis techniques , gene chip analysis , computational biology , identification (biology) , medicine , bioinformatics , biology , genetics , gene , gene expression , botany
The identification of clinically relevant genomic dosage anomalies assists in accurate diagnosis, prognosis, and medical management of affected individuals. Technological advancements within the field, such as the advent of microarray, have markedly increased the resolution of detection; however, clinical laboratories have maintained conventional techniques for confirmation of genomic imbalances identified by microarray to ensure diagnostic accuracy. In recent years the utility of this confirmatory testing of large-scale aberrations has been questioned but has not been scientifically addressed.

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