| Literature DB >> 22415865 |
Joris R Vermeesch1, Paul D Brady, Damien Sanlaville, Klaas Kok, Rosalind J Hastings.
Abstract
Whole-genome analysis using genome-wide arrays, also called "genomic arrays," "microarrays," or "arrays," has become the first-tier diagnostic test for patients with developmental abnormalities and/or intellectual disabilities. In addition to constitutional anomalies, genomic arrays are also used to diagnose acquired disorders. Despite the rapid implementation of these technologies in diagnostic laboratories, external quality control schemes (such as CEQA, EMQN, UK NEQAS, and the USA QA scheme CAP) and interlaboratory comparisons show that there are huge differences in quality, interpretation, and reporting among laboratories. We offer guidance to laboratories to help assure the quality of array experiments and to standardize minimum detection resolution, and we also provide guidelines to standardize interpretation and reporting.Entities:
Mesh:
Year: 2012 PMID: 22415865 DOI: 10.1002/humu.22076
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878