Literature DB >> 27493482

Clinical Diagnosis of Mendelian Disorders Using a Comprehensive Gene-Targeted Panel Test for Next-Generation Sequencing.

Tetsuya Okazaki1, Megumi Murata2, Masachika Kai3, Kaori Adachi2, Naoko Nakagawa4, Noriko Kasagi5, Wataru Matsumura1, Yoshihiro Maegaki6, Eiji Nanba7.   

Abstract

BACKGROUND: Genetic diagnoses provide beneficial information to patients and families. However, traditional genetic diagnoses are often difficult even for experienced clinicians and require recognition of characteristic patterns of signs or symptoms to guide targeted genetic testing for the confirmation of diagnoses. Next-generation sequencing (NGS) is a powerful genetic diagnostic tool. However, whole-genome and whole-exome sequencing (WES) are expensive, and the interpretation of results is difficult. Hence, target gene capture sequencing of gene panels has recently been applied to genetic diagnoses. Herein, we demonstrate that targeted sequencing approaches using gene panel testing are highly efficient for the diagnosis of Mendelian disorders.
METHODS: NGS using TruSight one gene panel was performed in 17 families and 20 patients, and we developed a bioinformatic pipeline at our institution for detecting mutations.
RESULTS: We detected causative mutations in 6 of 17 (35%) families. In particular, 11 (65%) families had syndromic diagnosis and 6 (35%) had no syndromic diagnosis before NGS testing. The number of positive diagnoses was 5 of 11 (45%) in the syndromic group and were 1 of 6 (17%) among patients of the no syndromic diagnosis group.
CONCLUSION: Diagnostic yields in the present study were higher than in previous reports of genetic and chromosomal tests and WES. The present comprehensive gene-targeted panel test is a powerful diagnostic tool for Mendelian disorders.

Entities:  

Keywords:  candidate gene analyses; diagnosis high-throughput DNA sequencing

Year:  2016        PMID: 27493482      PMCID: PMC4973017     

Source DB:  PubMed          Journal:  Yonago Acta Med        ISSN: 0513-5710            Impact factor:   1.641


  17 in total

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Authors:  Xi Lin; Wenxue Tang; Shoeb Ahmad; Jingqiao Lu; Candice C Colby; Jason Zhu; Qing Yu
Journal:  Hear Res       Date:  2012-01-14       Impact factor: 3.208

2.  A clinical and genetic overview of 18 years neurofibromatosis type 1 molecular diagnostics in the Netherlands.

Authors:  R van Minkelen; Y van Bever; J N R Kromosoeto; C J Withagen-Hermans; A Nieuwlaat; D J J Halley; A M W van den Ouweland
Journal:  Clin Genet       Date:  2013-06-25       Impact factor: 4.438

3.  Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies.

Authors:  Xiaohui Bai; Huaiqing Lv; Fengguo Zhang; Jinzhi Liu; Zhaomin Fan; Lei Xu; Yuhang Han; Renjie Chai; Jianfeng Li; Haibo Wang
Journal:  Am J Med Genet A       Date:  2014-09-23       Impact factor: 2.802

4.  Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.

Authors:  Takeshi Kato; Naoya Morisada; Hiroaki Nagase; Masahiro Nishiyama; Daisaku Toyoshima; Taku Nakagawa; Azusa Maruyama; Xue Jun Fu; Kandai Nozu; Hiroko Wada; Satoshi Takada; Kazumoto Iijima
Journal:  Brain Dev       Date:  2015-03-27       Impact factor: 1.961

5.  Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome.

Authors:  Tomasz Zemojtel; Sebastian Köhler; Luisa Mackenroth; Marten Jäger; Jochen Hecht; Peter Krawitz; Luitgard Graul-Neumann; Sandra Doelken; Nadja Ehmke; Malte Spielmann; Nancy Christine Oien; Michal R Schweiger; Ulrike Krüger; Götz Frommer; Björn Fischer; Uwe Kornak; Ricarda Flöttmann; Amin Ardeshirdavani; Yves Moreau; Suzanna E Lewis; Melissa Haendel; Damian Smedley; Denise Horn; Stefan Mundlos; Peter N Robinson
Journal:  Sci Transl Med       Date:  2014-09-03       Impact factor: 17.956

6.  Molecular findings among patients referred for clinical whole-exome sequencing.

Authors:  Yaping Yang; Donna M Muzny; Fan Xia; Zhiyv Niu; Richard Person; Yan Ding; Patricia Ward; Alicia Braxton; Min Wang; Christian Buhay; Narayanan Veeraraghavan; Alicia Hawes; Theodore Chiang; Magalie Leduc; Joke Beuten; Jing Zhang; Weimin He; Jennifer Scull; Alecia Willis; Megan Landsverk; William J Craigen; Mir Reza Bekheirnia; Asbjorg Stray-Pedersen; Pengfei Liu; Shu Wen; Wendy Alcaraz; Hong Cui; Magdalena Walkiewicz; Jeffrey Reid; Matthew Bainbridge; Ankita Patel; Eric Boerwinkle; Arthur L Beaudet; James R Lupski; Sharon E Plon; Richard A Gibbs; Christine M Eng
Journal:  JAMA       Date:  2014-11-12       Impact factor: 56.272

7.  Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome.

Authors:  Tony M F Tong; Edgar W L Hau; Ivan F M Lo; Daniel H C Chan; Stephen T S Lam
Journal:  Chin Med J (Engl)       Date:  2005-09-20       Impact factor: 2.628

8.  Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patients.

Authors:  M Duno; F Skovby; M Schwartz
Journal:  Ann Hum Genet       Date:  2007-06-11       Impact factor: 1.670

9.  A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.

Authors:  G A Bellus; I McIntosh; E A Smith; A S Aylsworth; I Kaitila; W A Horton; G A Greenhaw; J T Hecht; C A Francomano
Journal:  Nat Genet       Date:  1995-07       Impact factor: 38.330

10.  Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.

Authors:  Claire Redin; Bénédicte Gérard; Julia Lauer; Yvan Herenger; Jean Muller; Angélique Quartier; Alice Masurel-Paulet; Marjolaine Willems; Gaétan Lesca; Salima El-Chehadeh; Stéphanie Le Gras; Serge Vicaire; Muriel Philipps; Michaël Dumas; Véronique Geoffroy; Claire Feger; Nicolas Haumesser; Yves Alembik; Magalie Barth; Dominique Bonneau; Estelle Colin; Hélène Dollfus; Bérénice Doray; Marie-Ange Delrue; Valérie Drouin-Garraud; Elisabeth Flori; Mélanie Fradin; Christine Francannet; Alice Goldenberg; Serge Lumbroso; Michèle Mathieu-Dramard; Dominique Martin-Coignard; Didier Lacombe; Gilles Morin; Anne Polge; Sylvie Sukno; Christel Thauvin-Robinet; Julien Thevenon; Martine Doco-Fenzy; David Genevieve; Pierre Sarda; Patrick Edery; Bertrand Isidor; Bernard Jost; Laurence Olivier-Faivre; Jean-Louis Mandel; Amélie Piton
Journal:  J Med Genet       Date:  2014-08-28       Impact factor: 6.318

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  9 in total

1.  Duchenne muscular dystrophy-like phenotype in an LGMD2I patient with novel FKRP gene variants.

Authors:  Tetsuya Okazaki; Kaori Matsuura; Noriko Kasagi; Kaori Adachi; Masachika Kai; Mariko Okubo; Ichizo Nishino; Eiji Nanba; Yoshihiro Maegaki
Journal:  Hum Genome Var       Date:  2020-04-20

2.  Determination of disease phenotypes and pathogenic variants from exome sequence data in the CAGI 4 gene panel challenge.

Authors:  Kunal Kundu; Lipika R Pal; Yizhou Yin; John Moult
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3.  Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders.

Authors:  Marie Beaumont; Linda Akloul; Wilfrid Carré; Chloé Quélin; Hubert Journel; Laurent Pasquier; Mélanie Fradin; Sylvie Odent; Houda Hamdi-Rozé; Erwan Watrin; Valérie Dupé; Christèle Dubourg; Véronique David
Journal:  Hum Genet       Date:  2019-03-05       Impact factor: 4.132

4.  Targeted sequencing approach to identify genetic mutations in Nasu-Hakola disease.

Authors:  Jun-Ichi Satoh; Motoaki Yanaizu; Youhei Tosaki; Kenji Sakai; Yoshihiro Kino
Journal:  Intractable Rare Dis Res       Date:  2016-11

Review 5.  Next Generation Sequencing and Bioinformatics Analysis of Family Genetic Inheritance.

Authors:  Aquillah M Kanzi; James Emmanuel San; Benjamin Chimukangara; Eduan Wilkinson; Maryam Fish; Veron Ramsuran; Tulio de Oliveira
Journal:  Front Genet       Date:  2020-10-23       Impact factor: 4.599

6.  Clinical utility in infants with suspected monogenic conditions through next-generation sequencing.

Authors:  Sha Hong; Li Wang; Dongying Zhao; Yonghong Zhang; Yan Chen; Jintong Tan; Lili Liang; Tianwen Zhu
Journal:  Mol Genet Genomic Med       Date:  2019-04-09       Impact factor: 2.183

7.  Duchenne muscular dystrophy-like phenotype in an LGMD2I patient with novel FKRP gene variants.

Authors:  Tetsuya Okazaki; Kaori Matsuura; Noriko Kasagi; Kaori Adachi; Masachika Kai; Mariko Okubo; Ichizo Nishino; Eiji Nanba; Yoshihiro Maegaki
Journal:  Hum Genome Var       Date:  2020-04-20

8.  Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations.

Authors:  Yuki Kawashima-Sonoyama; Tomoyuki Hotsubo; Takashi Hamajima; Naoki Hamajima; Masanobu Fujimoto; Noriyuki Namba; Susumu Kanzaki
Journal:  Clin Pediatr Endocrinol       Date:  2022-02-07

9.  Comparison of Causative Variant Prioritization Tools Using Next-generation Sequencing Data in Japanese Patients with Mendelian Disorders.

Authors:  Mitsutaka Ebiki; Tetsuya Okazaki; Masachika Kai; Kaori Adachi; Eiji Nanba
Journal:  Yonago Acta Med       Date:  2019-09-13       Impact factor: 1.641

  9 in total

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