Literature DB >> 25326637

Clinical exome sequencing for genetic identification of rare Mendelian disorders.

Hane Lee1, Joshua L Deignan1, Naghmeh Dorrani2, Samuel P Strom1, Sibel Kantarci1, Fabiola Quintero-Rivera1, Kingshuk Das1, Traci Toy1, Bret Harry3, Michael Yourshaw4, Michelle Fox4, Brent L Fogel5, Julian A Martinez-Agosto6, Derek A Wong4, Vivian Y Chang4, Perry B Shieh5, Christina G S Palmer7, Katrina M Dipple6, Wayne W Grody8, Eric Vilain9, Stanley F Nelson10.   

Abstract

IMPORTANCE: Clinical exome sequencing (CES) is rapidly becoming a common molecular diagnostic test for individuals with rare genetic disorders.
OBJECTIVE: To report on initial clinical indications for CES referrals and molecular diagnostic rates for different indications and for different test types. DESIGN, SETTING, AND PARTICIPANTS: Clinical exome sequencing was performed on 814 consecutive patients with undiagnosed, suspected genetic conditions at the University of California, Los Angeles, Clinical Genomics Center between January 2012 and August 2014. Clinical exome sequencing was conducted as trio-CES (both parents and their affected child sequenced simultaneously) to effectively detect de novo and compound heterozygous variants or as proband-CES (only the affected individual sequenced) when parental samples were not available. MAIN OUTCOMES AND MEASURES: Clinical indications for CES requests, molecular diagnostic rates of CES overall and for phenotypic subgroups, and differences in molecular diagnostic rates between trio-CES and proband-CES.
RESULTS: Of the 814 cases, the overall molecular diagnosis rate was 26% (213 of 814; 95% CI, 23%-29%). The molecular diagnosis rate for trio-CES was 31% (127 of 410 cases; 95% CI, 27%-36%) and 22% (74 of 338 cases; 95% CI, 18%-27%) for proband-CES. In cases of developmental delay in children (<5 years, n = 138), the molecular diagnosis rate was 41% (45 of 109; 95% CI, 32%-51%) for trio-CES cases and 9% (2 of 23, 95% CI, 1%-28%) for proband-CES cases. The significantly higher diagnostic yield (P value = .002; odds ratio, 7.4 [95% CI, 1.6-33.1]) of trio-CES was due to the identification of de novo and compound heterozygous variants. CONCLUSIONS AND RELEVANCE: In this sample of patients with undiagnosed, suspected genetic conditions, trio-CES was associated with higher molecular diagnostic yield than proband-CES or traditional molecular diagnostic methods. Additional studies designed to validate these findings and to explore the effect of this approach on clinical and economic outcomes are warranted.

Entities:  

Mesh:

Year:  2014        PMID: 25326637      PMCID: PMC4278636          DOI: 10.1001/jama.2014.14604

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  21 in total

1.  UPD detection using homozygosity profiling with a SNP genotyping microarray.

Authors:  Peter Papenhausen; Stuart Schwartz; Hiba Risheg; Elisabeth Keitges; Inder Gadi; Rachel D Burnside; Vikram Jaswaney; John Pappas; Romela Pasion; Kenneth Friedman; James Tepperberg
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

2.  Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy.

Authors:  Sarah E Heron; Katherine R Smith; Melanie Bahlo; Lino Nobili; Esther Kahana; Laura Licchetta; Karen L Oliver; Aziz Mazarib; Zaid Afawi; Amos Korczyn; Giuseppe Plazzi; Steven Petrou; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Nat Genet       Date:  2012-10-21       Impact factor: 38.330

3.  Rich annotation of DNA sequencing variants by leveraging the Ensembl Variant Effect Predictor with plugins.

Authors:  Michael Yourshaw; S Paige Taylor; Aliz R Rao; Martín G Martín; Stanley F Nelson
Journal:  Brief Bioinform       Date:  2014-03-12       Impact factor: 11.622

4.  Not-so-incidental findings: the ACMG recommendations on the reporting of incidental findings in clinical whole genome and whole exome sequencing.

Authors:  Megan Allyse; Marsha Michie
Journal:  Trends Biotechnol       Date:  2013-05-09       Impact factor: 19.536

5.  A systematic approach to assessing the clinical significance of genetic variants.

Authors:  H Duzkale; J Shen; H McLaughlin; A Alfares; M A Kelly; T J Pugh; B H Funke; H L Rehm; M S Lebo
Journal:  Clin Genet       Date:  2013-11       Impact factor: 4.438

6.  ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Authors:  C Sue Richards; Sherri Bale; Daniel B Bellissimo; Soma Das; Wayne W Grody; Madhuri R Hegde; Elaine Lyon; Brian E Ward
Journal:  Genet Med       Date:  2008-04       Impact factor: 8.822

7.  American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.

Authors:  Catherine W Rehder; Karen L David; Betsy Hirsch; Helga V Toriello; Carolyn M Wilson; Hutton M Kearney
Journal:  Genet Med       Date:  2013-01-17       Impact factor: 8.822

8.  ACMG recommendations on incidental findings are flawed scientifically and ethically.

Authors:  Neil A Holtzman
Journal:  Genet Med       Date:  2013-09       Impact factor: 8.822

9.  Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.

Authors:  Brian J O'Roak; Laura Vives; Santhosh Girirajan; Emre Karakoc; Niklas Krumm; Bradley P Coe; Roie Levy; Arthur Ko; Choli Lee; Joshua D Smith; Emily H Turner; Ian B Stanaway; Benjamin Vernot; Maika Malig; Carl Baker; Beau Reilly; Joshua M Akey; Elhanan Borenstein; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Jay Shendure; Evan E Eichler
Journal:  Nature       Date:  2012-04-04       Impact factor: 49.962

10.  ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Authors:  Robert C Green; Jonathan S Berg; Wayne W Grody; Sarah S Kalia; Bruce R Korf; Christa L Martin; Amy L McGuire; Robert L Nussbaum; Julianne M O'Daniel; Kelly E Ormond; Heidi L Rehm; Michael S Watson; Marc S Williams; Leslie G Biesecker
Journal:  Genet Med       Date:  2013-06-20       Impact factor: 8.822

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  389 in total

Review 1.  The frontiers of sequencing in undiagnosed neurodevelopmental diseases.

Authors:  Hane Lee; Stanley F Nelson
Journal:  Curr Opin Genet Dev       Date:  2020-06-27       Impact factor: 5.578

2.  Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development.

Authors:  Asaf Vivante; Marc-Jens Kleppa; Julian Schulz; Stefan Kohl; Amita Sharma; Jing Chen; Shirlee Shril; Daw-Yang Hwang; Anna-Carina Weiss; Michael M Kaminski; Rachel Shukrun; Markus J Kemper; Anja Lehnhardt; Rolf Beetz; Simone Sanna-Cherchi; Miguel Verbitsky; Ali G Gharavi; Helen M Stuart; Sally A Feather; Judith A Goodship; Timothy H J Goodship; Adrian S Woolf; Sjirk J Westra; Daniel P Doody; Stuart B Bauer; Richard S Lee; Rosalyn M Adam; Weining Lu; Heiko M Reutter; Elijah O Kehinde; Erika J Mancini; Richard P Lifton; Velibor Tasic; Soeren S Lienkamp; Harald Jüppner; Andreas Kispert; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2015-07-30       Impact factor: 11.025

Review 3.  Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing.

Authors:  Jodi Warman Chardon; Chandree Beaulieu; Taila Hartley; Kym M Boycott; David A Dyment
Journal:  Curr Neurol Neurosci Rep       Date:  2015-09       Impact factor: 5.081

4.  A novel CRX mutation by whole-exome sequencing in an autosomal dominant cone-rod dystrophy pedigree.

Authors:  Qin-Kang Lu; Na Zhao; Ya-Su Lv; Wei-Kun Gong; Hui-Yun Wang; Qi-Hu Tong; Xiao-Ming Lai; Rong-Rong Liu; Ming-Yan Fang; Jian-Guo Zhang; Zhen-Fang Du; Xian-Ning Zhang
Journal:  Int J Ophthalmol       Date:  2015-12-18       Impact factor: 1.779

Review 5.  Exploring the genetic basis of early-onset chronic kidney disease.

Authors:  Asaf Vivante; Friedhelm Hildebrandt
Journal:  Nat Rev Nephrol       Date:  2016-01-11       Impact factor: 28.314

6.  Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield.

Authors:  S Anazi; S Maddirevula; E Faqeih; H Alsedairy; F Alzahrani; H E Shamseldin; N Patel; M Hashem; N Ibrahim; F Abdulwahab; N Ewida; H S Alsaif; H Al Sharif; W Alamoudi; A Kentab; F A Bashiri; M Alnaser; A H AlWadei; M Alfadhel; W Eyaid; A Hashem; A Al Asmari; M M Saleh; A AlSaman; K A Alhasan; M Alsughayir; M Al Shammari; A Mahmoud; Z N Al-Hassnan; M Al-Husain; R Osama Khalil; N Abd El Meguid; A Masri; R Ali; T Ben-Omran; P El Fishway; A Hashish; A Ercan Sencicek; M State; A M Alazami; M A Salih; N Altassan; S T Arold; M Abouelhoda; S M Wakil; D Monies; R Shaheen; F S Alkuraya
Journal:  Mol Psychiatry       Date:  2016-07-19       Impact factor: 15.992

7.  De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay.

Authors:  Valerie A Arboleda; Hane Lee; Naghmeh Dorrani; Neda Zadeh; Mary Willis; Colleen Forsyth Macmurdo; Melanie A Manning; Andrea Kwan; Louanne Hudgins; Florian Barthelemy; M Carrie Miceli; Fabiola Quintero-Rivera; Sibel Kantarci; Samuel P Strom; Joshua L Deignan; Wayne W Grody; Eric Vilain; Stanley F Nelson
Journal:  Am J Hum Genet       Date:  2015-02-26       Impact factor: 11.025

8.  The Genetic Landscape of Diamond-Blackfan Anemia.

Authors:  Jacob C Ulirsch; Jeffrey M Verboon; Shideh Kazerounian; Michael H Guo; Daniel Yuan; Leif S Ludwig; Robert E Handsaker; Nour J Abdulhay; Claudia Fiorini; Giulio Genovese; Elaine T Lim; Aaron Cheng; Beryl B Cummings; Katherine R Chao; Alan H Beggs; Casie A Genetti; Colin A Sieff; Peter E Newburger; Edyta Niewiadomska; Michal Matysiak; Adrianna Vlachos; Jeffrey M Lipton; Eva Atsidaftos; Bertil Glader; Anupama Narla; Pierre-Emmanuel Gleizes; Marie-Françoise O'Donohue; Nathalie Montel-Lehry; David J Amor; Steven A McCarroll; Anne H O'Donnell-Luria; Namrata Gupta; Stacey B Gabriel; Daniel G MacArthur; Eric S Lander; Monkol Lek; Lydie Da Costa; David G Nathan; Andrei A Korostelev; Ron Do; Vijay G Sankaran; Hanna T Gazda
Journal:  Am J Hum Genet       Date:  2018-11-29       Impact factor: 11.025

9.  Exome Sequencing in Children.

Authors:  Elisa A Mahler; Jessika Johannsen; Konstantinos Tsiakas; Katja Kloth; Sabine Lüttgen; Chris Mühlhausen; Bader Alhaddad; Tobias B Haack; Tim M Strom; Fanny Kortüm; Thomas Meitinger; Ania C Muntau; René Santer; Christian Kubisch; Davor Lessel; Jonas Denecke; Maja Hempel
Journal:  Dtsch Arztebl Int       Date:  2019-03-22       Impact factor: 5.594

10.  A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease.

Authors:  Damian Smedley; Max Schubach; Julius O B Jacobsen; Sebastian Köhler; Tomasz Zemojtel; Malte Spielmann; Marten Jäger; Harry Hochheiser; Nicole L Washington; Julie A McMurry; Melissa A Haendel; Christopher J Mungall; Suzanna E Lewis; Tudor Groza; Giorgio Valentini; Peter N Robinson
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

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