Literature DB >> 22415865

Genome-wide arrays: quality criteria and platforms to be used in routine diagnostics.

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.
© 2012 Wiley Periodicals, Inc.

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Year:  2012        PMID: 22415865     DOI: 10.1002/humu.22076

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  25 in total

1.  Whole-genome sequencing in health care. Recommendations of the European Society of Human Genetics.

Authors:  Carla G van El; Martina C Cornel; Pascal Borry; Ros J Hastings; Florence Fellmann; Shirley V Hodgson; Heidi C Howard; Anne Cambon-Thomsen; Bartha M Knoppers; Hanne Meijers-Heijboer; Hans Scheffer; Lisbeth Tranebjaerg; Wybo Dondorp; Guido M W R de Wert
Journal:  Eur J Hum Genet       Date:  2013-06       Impact factor: 4.246

2.  Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.

Authors:  Carla G van El; Martina C Cornel; Pascal Borry; Ros J Hastings; Florence Fellmann; Shirley V Hodgson; Heidi C Howard; Anne Cambon-Thomsen; Bartha M Knoppers; Hanne Meijers-Heijboer; Hans Scheffer; Lisbeth Tranebjaerg; Wybo Dondorp; Guido M W R de Wert
Journal:  Eur J Hum Genet       Date:  2013-06       Impact factor: 4.246

3.  High-resolution copy number variation analysis of schizophrenia in Japan.

Authors:  I Kushima; B Aleksic; M Nakatochi; T Shimamura; T Shiino; A Yoshimi; H Kimura; Y Takasaki; C Wang; J Xing; K Ishizuka; T Oya-Ito; Y Nakamura; Y Arioka; T Maeda; M Yamamoto; M Yoshida; H Noma; S Hamada; M Morikawa; Y Uno; T Okada; T Iidaka; S Iritani; T Yamamoto; M Miyashita; A Kobori; M Arai; M Itokawa; M-C Cheng; Y-A Chuang; C-H Chen; M Suzuki; T Takahashi; R Hashimoto; H Yamamori; Y Yasuda; Y Watanabe; A Nunokawa; T Someya; M Ikeda; T Toyota; T Yoshikawa; S Numata; T Ohmori; S Kunimoto; D Mori; N Iwata; N Ozaki
Journal:  Mol Psychiatry       Date:  2016-05-31       Impact factor: 15.992

Review 4.  Prenatal and pre-implantation genetic diagnosis.

Authors:  Joris Robert Vermeesch; Thierry Voet; Koenraad Devriendt
Journal:  Nat Rev Genet       Date:  2016-09-15       Impact factor: 53.242

5.  Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system.

Authors:  Lucía Daniela Espeche; Andrea Paula Solari; María Ángeles Mori; Rubén Martín Arenas; María Palomares; Myriam Pérez; Cinthia Martínez; Vanesa Lotersztein; Mabel Segovia; Romina Armando; Liliana Beatriz Dain; Julián Nevado; Pablo Lapunzina; Sandra Rozental
Journal:  Mol Biol Rep       Date:  2020-09-13       Impact factor: 2.316

6.  PIAS4 is associated with macro/microcephaly in the novel interstitial 19p13.3 microdeletion/microduplication syndrome.

Authors:  Julián Nevado; Jill A Rosenfeld; Rocío Mena; María Palomares-Bralo; Elena Vallespín; María Ángeles Mori; Jair A Tenorio; Karen W Gripp; Elizabeth Denenberg; Miguel Del Campo; Alberto Plaja; Rubén Martín-Arenas; Fernando Santos-Simarro; Lluis Armengol; Gordon Gowans; María Orera; M Carmen Sanchez-Hombre; Esther Corbacho-Fernández; Alberto Fernández-Jaén; Chad Haldeman-Englert; Sulagna Saitta; Holly Dubbs; Duban B Bénédicte; Xia Li; Lani Devaney; Mary Beth Dinulos; Stephanie Vallee; M Carmen Crespo; Blanca Fernández; Victoria E Fernández-Montaño; Inmaculada Rueda-Arenas; María Luisa de Torres; Jay W Ellison; Salmo Raskin; Carlos A Venegas-Vega; Fernando Fernández-Ramírez; Alicia Delicado; Sixto García-Miñaúr; Pablo Lapunzina
Journal:  Eur J Hum Genet       Date:  2015-04-08       Impact factor: 4.246

Review 7.  Genomic medicine for kidney disease.

Authors:  Emily E Groopman; Hila Milo Rasouly; Ali G Gharavi
Journal:  Nat Rev Nephrol       Date:  2018-01-08       Impact factor: 28.314

Review 8.  Genetic testing for kidney disease of unknown etiology.

Authors:  Thomas Hays; Emily E Groopman; Ali G Gharavi
Journal:  Kidney Int       Date:  2020-04-24       Impact factor: 10.612

9.  Diagnostic interpretation of array data using public databases and internet sources.

Authors:  Nicole de Leeuw; Trijnie Dijkhuizen; Jayne Y Hehir-Kwa; Nigel P Carter; Lars Feuk; Helen V Firth; Robert M Kuhn; David H Ledbetter; Christa Lese Martin; Conny M A van Ravenswaaij-Arts; Steven W Scherer; Soheil Shams; Steven Van Vooren; Rolf Sijmons; Morris Swertz; Ros Hastings
Journal:  Hum Mutat       Date:  2012-06       Impact factor: 4.878

10.  Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations.

Authors:  Sarah Vergult; Ellen Van Binsbergen; Tom Sante; Silke Nowak; Olivier Vanakker; Kathleen Claes; Bruce Poppe; Nathalie Van der Aa; Markus J van Roosmalen; Karen Duran; Masoumeh Tavakoli-Yaraki; Marielle Swinkels; Marie-José van den Boogaard; Mieke van Haelst; Filip Roelens; Frank Speleman; Edwin Cuppen; Geert Mortier; Wigard P Kloosterman; Björn Menten
Journal:  Eur J Hum Genet       Date:  2013-10-09       Impact factor: 4.246

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