Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions

Author:

Lavelle Tara A.ORCID,Feng Xue,Keisler Marlena,Cohen Joshua T.,Neumann Peter J.,Prichard Daryl,Schroeder Brock E.,Salyakina Daria,Espinal Paula S.,Weidner Samuel B.,Maron Jill L.

Funder

Merck

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference44 articles.

1. Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG);Manickam;Genet Med,2021

2. GeneDx, Inc. January 17, 2021. https://www.genedx.com/. Accessed December 29, 2020.

3. Baylor Genetics Laboratories. Medical Genetics Test Details. https://www.bcm.edu/research/medical-genetics-labs/. Accessed August 16, 2016.

4. Private payer coverage policies for exome sequencing (ES) in pediatric patients: trends over time and analysis of evidence cited;Douglas;Genet Med,2019

5. Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature;Schwarze;Genet Med,2018

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