Literature DB >> 34930662

Genome sequencing as a first-line diagnostic test for hospitalized infants.

Kevin M Bowling1, Michelle L Thompson1, Candice R Finnila1, Susan M Hiatt1, Donald R Latner1, Michelle D Amaral1, James M J Lawlor1, Kelly M East1, Meagan E Cochran1, Veronica Greve1, Whitley V Kelley1, David E Gray1, Stephanie A Felker2, Hannah Meddaugh3, Ashley Cannon4, Amanda Luedecke4, Kelly E Jackson5, Laura G Hendon6, Hillary M Janani7, Marla Johnston7, Lee Ann Merin8, Sarah L Deans5, Carly Tuura6, Heather Williams6, Kelly Laborde9, Matthew B Neu10, Jessica Patrick-Esteve7, Anna C E Hurst4, Jegen Kandasamy8, Wally Carlo8, Kyle B Brothers5, Brian M Kirmse6, Renate Savich6, Duane Superneau11, Steven B Spedale12, Sara J Knight13, Gregory S Barsh1, Bruce R Korf4, Gregory M Cooper14.   

Abstract

PURPOSE: SouthSeq is a translational research study that undertook genome sequencing (GS) for infants with symptoms suggestive of a genetic disorder. Recruitment targeted racial/ethnic minorities and rural, medically underserved areas in the Southeastern United States, which are historically underrepresented in genomic medicine research.
METHODS: GS and analysis were performed for 367 infants to detect disease-causal variation concurrent with standard of care evaluation and testing.
RESULTS: Definitive diagnostic (DD) or likely diagnostic (LD) genetic findings were identified in 30% of infants, and 14% of infants harbored an uncertain result. Only 43% of DD/LD findings were identified via concurrent clinical genetic testing, suggesting that GS testing is better for obtaining early genetic diagnosis. We also identified phenotypes that correlate with the likelihood of receiving a DD/LD finding, such as craniofacial, ophthalmologic, auditory, skin, and hair abnormalities. We did not observe any differences in diagnostic rates between racial/ethnic groups.
CONCLUSION: We describe one of the largest-to-date GS cohorts of ill infants, enriched for African American and rural patients. Our results show the utility of GS because it provides early-in-life detection of clinically relevant genetic variations not detected by current clinical genetic testing, particularly for infants exhibiting certain phenotypic features.
Copyright © 2021 American College of Medical Genetics and Genomics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Diagnostic yield; Genetic diagnosis; Genome sequencing; Infants; Utility

Mesh:

Year:  2021        PMID: 34930662      PMCID: PMC8995345          DOI: 10.1016/j.gim.2021.11.020

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.864


  35 in total

1.  CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing.

Authors:  Alexej Abyzov; Alexander E Urban; Michael Snyder; Mark Gerstein
Journal:  Genome Res       Date:  2011-02-07       Impact factor: 9.043

Review 2.  The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.

Authors:  Jessica X Chong; Kati J Buckingham; Shalini N Jhangiani; Corinne Boehm; Nara Sobreira; Joshua D Smith; Tanya M Harrell; Margaret J McMillin; Wojciech Wiszniewski; Tomasz Gambin; Zeynep H Coban Akdemir; Kimberly Doheny; Alan F Scott; Dimitri Avramopoulos; Aravinda Chakravarti; Julie Hoover-Fong; Debra Mathews; P Dane Witmer; Hua Ling; Kurt Hetrick; Lee Watkins; Karynne E Patterson; Frederic Reinier; Elizabeth Blue; Donna Muzny; Martin Kircher; Kaya Bilguvar; Francesc López-Giráldez; V Reid Sutton; Holly K Tabor; Suzanne M Leal; Murat Gunel; Shrikant Mane; Richard A Gibbs; Eric Boerwinkle; Ada Hamosh; Jay Shendure; James R Lupski; Richard P Lifton; David Valle; Deborah A Nickerson; Michael J Bamshad
Journal:  Am J Hum Genet       Date:  2015-07-09       Impact factor: 11.025

3.  A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis.

Authors:  Tiong Yang Tan; Sebastian Lunke; Belinda Chong; Dean Phelan; Miriam Fanjul-Fernandez; Justine E Marum; Vanessa Siva Kumar; Zornitza Stark; Alison Yeung; Natasha J Brown; Chloe Stutterd; Martin B Delatycki; Simon Sadedin; Melissa Martyn; Ilias Goranitis; Natalie Thorne; Clara L Gaff; Susan M White
Journal:  Eur J Hum Genet       Date:  2019-07-18       Impact factor: 4.246

4.  Using ERDS to infer copy-number variants in high-coverage genomes.

Authors:  Mingfu Zhu; Anna C Need; Yujun Han; Dongliang Ge; Jessica M Maia; Qianqian Zhu; Erin L Heinzen; Elizabeth T Cirulli; Kimberly Pelak; Min He; Elizabeth K Ruzzo; Curtis Gumbs; Abanish Singh; Sheng Feng; Kevin V Shianna; David B Goldstein
Journal:  Am J Hum Genet       Date:  2012-08-30       Impact factor: 11.025

Review 5.  Paediatric genomics: diagnosing rare disease in children.

Authors:  Caroline F Wright; David R FitzPatrick; Helen V Firth
Journal:  Nat Rev Genet       Date:  2018-02-05       Impact factor: 53.242

6.  Genetic Misdiagnoses and the Potential for Health Disparities.

Authors:  Arjun K Manrai; Birgit H Funke; Heidi L Rehm; Morten S Olesen; Bradley A Maron; Peter Szolovits; David M Margulies; Joseph Loscalzo; Isaac S Kohane
Journal:  N Engl J Med       Date:  2016-08-18       Impact factor: 91.245

7.  Phenotype-driven variant filtration strategy in exome sequencing toward a high diagnostic yield and identification of 85 novel variants in 400 patients with rare Mendelian disorders.

Authors:  Nikolaos M Marinakis; Maria Svingou; Danai Veltra; Kyriaki Kekou; Christalena Sofocleous; Faidon-Nikolaos Tilemis; Konstantina Kosma; Eirini Tsoutsou; Helen Fryssira; Joanne Traeger-Synodinos
Journal:  Am J Med Genet A       Date:  2021-05-19       Impact factor: 2.802

8.  Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy.

Authors:  Katherine I Kendig; Saurabh Baheti; Matthew A Bockol; Travis M Drucker; Steven N Hart; Jacob R Heldenbrand; Mikel Hernaez; Matthew E Hudson; Michael T Kalmbach; Eric W Klee; Nathan R Mattson; Christian A Ross; Morgan Taschuk; Eric D Wieben; Mathieu Wiepert; Derek E Wildman; Liudmila S Mainzer
Journal:  Front Genet       Date:  2019-08-20       Impact factor: 4.599

9.  Genome-wide sequencing in acutely ill infants: genomic medicine's critical application?

Authors:  Jan M Friedman; Yvonne Bombard; Martina C Cornel; Conrad V Fernandez; Anne K Junker; Sharon E Plon; Zornitza Stark; Bartha Maria Knoppers
Journal:  Genet Med       Date:  2018-06-12       Impact factor: 8.822

10.  A structural variation reference for medical and population genetics.

Authors:  Ryan L Collins; Harrison Brand; Konrad J Karczewski; Xuefang Zhao; Jessica Alföldi; Laurent C Francioli; Amit V Khera; Chelsea Lowther; Laura D Gauthier; Harold Wang; Nicholas A Watts; Matthew Solomonson; Anne O'Donnell-Luria; Alexander Baumann; Ruchi Munshi; Mark Walker; Christopher W Whelan; Yongqing Huang; Ted Brookings; Ted Sharpe; Matthew R Stone; Elise Valkanas; Jack Fu; Grace Tiao; Kristen M Laricchia; Valentin Ruano-Rubio; Christine Stevens; Namrata Gupta; Caroline Cusick; Lauren Margolin; Kent D Taylor; Henry J Lin; Stephen S Rich; Wendy S Post; Yii-Der Ida Chen; Jerome I Rotter; Chad Nusbaum; Anthony Philippakis; Eric Lander; Stacey Gabriel; Benjamin M Neale; Sekar Kathiresan; Mark J Daly; Eric Banks; Daniel G MacArthur; Michael E Talkowski
Journal:  Nature       Date:  2020-05-27       Impact factor: 69.504

View more
  2 in total

1.  Measures of Utility Among Studies of Genomic Medicine for Critically Ill Infants: A Systematic Review.

Authors:  Katharine Press Callahan; Rebecca Mueller; John Flibotte; Emily A Largent; Chris Feudtner
Journal:  JAMA Netw Open       Date:  2022-08-01

2.  Education and Training of Non-Genetics Providers on the Return of Genome Sequencing Results in a NICU Setting.

Authors:  Kelly M East; Meagan E Cochran; Whitley V Kelley; Veronica Greve; Candice R Finnila; Tanner Coleman; Mikayla Jennings; Latonya Alexander; Elizabeth J Rahn; Maria I Danila; Greg Barsh; Bruce Korf; Greg Cooper
Journal:  J Pers Med       Date:  2022-03-05
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.