Literature DB >> 34131312

Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).

Lina Shao1, Yassmine Akkari2, Linda D Cooley3,4, David T Miller5, Bryce A Seifert6, Daynna J Wolff7, Fady M Mikhail8.   

Abstract

Chromosomal microarray technologies, including array comparative genomic hybridization and single-nucleotide polymorphism array, are widely applied in the diagnostic evaluation for both constitutional and neoplastic disorders. In a constitutional setting, this technology is accepted as the first-tier test for the evaluation of chromosomal imbalances associated with intellectual disability, autism, and/or multiple congenital anomalies. Furthermore, chromosomal microarray analysis is recommended for patients undergoing invasive prenatal diagnosis with one or more major fetal structural abnormalities identified by ultrasonographic examination, and in the evaluation of intrauterine fetal demise or stillbirth when further cytogenetic analysis is desired. This technology also provides important genomic data in the diagnosis, prognosis, and therapy of neoplastic disorders, including both hematologic malignancies and solid tumors. To assist clinical laboratories in the validation of chromosomal microarray methodologies for constitutional and neoplastic applications, the American College of Medical Genetics and Genomics (ACMG) Laboratory Quality Assurance Committee has developed these updated technical laboratory standards, which replace the ACMG technical standards and guidelines for microarray analysis in constitutional and neoplastic disorders previously published in 2013.
© 2021. The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics.

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Mesh:

Year:  2021        PMID: 34131312     DOI: 10.1038/s41436-021-01214-w

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  4 in total

1.  Genomic testing for copy number and single nucleotide variants in spermatogenic failure.

Authors:  J Hardy; N Pollock; T Gingrich; P Sweet; A Ramesh; J Kuong; A Basar; H Jiang; K Hwang; J Vukina; T Jaffe; M Olszewska; M Kurpisz; A N Yatsenko
Journal:  J Assist Reprod Genet       Date:  2022-07-18       Impact factor: 3.357

2.  Prenatal Diagnosis Using Chromosomal Microarray Analysis in High-Risk Pregnancies.

Authors:  Ching-Hua Hsiao; Jia-Shing Chen; Yu-Ming Shiao; Yann-Jang Chen; Ching-Hsuan Chen; Woei-Chyn Chu; Yi-Cheng Wu
Journal:  J Clin Med       Date:  2022-06-23       Impact factor: 4.964

3.  Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.

Authors:  Bo Yuan; Katharina V Schulze; Nurit Assia Batzir; Jefferson Sinson; Hongzheng Dai; Wenmiao Zhu; Francia Bocanegra; Chin-To Fong; Jimmy Holder; Joanne Nguyen; Christian P Schaaf; Yaping Yang; Weimin Bi; Christine Eng; Chad Shaw; James R Lupski; Pengfei Liu
Journal:  Genome Med       Date:  2022-09-30       Impact factor: 15.266

Review 4.  Clinical exome sequencing-Mistakes and caveats.

Authors:  Jordi Corominas; Sanne P Smeekens; Marcel R Nelen; Helger G Yntema; Erik-Jan Kamsteeg; Rolph Pfundt; Christian Gilissen
Journal:  Hum Mutat       Date:  2022-03-15       Impact factor: 4.700

  4 in total

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