Literature DB >> 25067876

Expansion of genetic testing in the division of functional genomics, research center for bioscience and technology, tottori university from 2000 to 2013.

Kaori Adachi1.   

Abstract

BACKGROUND: At the Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University, we have been making an effort to establish a genetic testing facility that can provide the same screening procedures conducted worldwide.
METHODS: Direct Sequencing of PCR products is the main method to detect point mutations, small deletions and insertions. Multiplex Ligation-dependent Probe Amplification (MLPA) was used to detect large deletions or insertions. Expansion of the repeat was analyzed for triplet repeat diseases. Original primers were constructed for 41 diseases when the reported primers failed to amplify the gene. Prediction of functional effects of human nsSNPs (PolyPhen) was used for evaluation of novel mutations.
RESULTS: From January 2000 to September 2013, a total of 1,006 DNA samples were subjected to genetic testing in the Division of Functional Genomics, Research Center for Bioscience and Technology, Tottori University. The hospitals that requested genetic testing were located in 43 prefectures in Japan and in 11 foreign countries. The genetic testing covered 62 diseases, and mutations were detected in 287 out of 1,006 with an average mutation detection rate of 24.7%. There were 77 samples for prenatal diagnosis. The number of samples has rapidly increased since 2010.
CONCLUSION: In 2013, the next-generation sequencers were introduced in our facility and are expected to provide more comprehensive genetic testing in the near future. Nowadays, genetic testing is a popular and powerful tool for diagnosis of many genetic diseases. Our genetic testing should be further expanded in the future.

Entities:  

Keywords:  genetic testing; germ-line mutation; prenatal diagnosis

Year:  2014        PMID: 25067876      PMCID: PMC4110691     

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


  25 in total

1.  Next-generation sequencing for clinical diagnostics.

Authors:  Howard J Jacob
Journal:  N Engl J Med       Date:  2013-10-02       Impact factor: 91.245

Review 2.  De novo mutations in human genetic disease.

Authors:  Joris A Veltman; Han G Brunner
Journal:  Nat Rev Genet       Date:  2012-07-18       Impact factor: 53.242

3.  Novel mutations in the gene encoding acid α-1,4-glucosidase in a patient with late-onset glycogen storage disease type II (Pompe disease) with impaired intelligence.

Authors:  Tomie Muraoka; Koji Murao; Hitomi Imachi; Fumi Kikuchi; Takuo Yoshimoto; Hisakazu Iwama; Hitoshi Hosokawa; Ichizo Nishino; Tokiko Fukuda; Hideo Sugie; Kaori Adachi; Eiji Nanba; Toshihiko Ishida
Journal:  Intern Med       Date:  2011-12-15       Impact factor: 1.271

4.  Non-radioactive DNA diagnosis for the fragile X syndrome in mentally retarded Japanese males.

Authors:  E Nanba; Y Kohno; A Matsuda; M Yano; C Sato; K Hashimoto; T Koeda; K Yoshino; M Kimura; Y Maeoka
Journal:  Brain Dev       Date:  1995 Sep-Oct       Impact factor: 1.961

5.  Clinical and serial MRI findings of a sialidosis type I patient with a novel missense mutation in the NEU1 gene.

Authors:  Yoshiki Sekijima; Katsuya Nakamura; Dai Kishida; Aya Narita; Kaori Adachi; Kosaku Ohno; Eiji Nanba; Shu-Ichi Ikeda
Journal:  Intern Med       Date:  2013-01-01       Impact factor: 1.271

6.  Allele frequency of human endothelial nitric oxide synthase gene polymorphism in abdominal aortic aneurysm.

Authors:  K Kotani; T Shimomura; F Murakami; S Ikawa; Y Kanaoka; S Ohgi; K Adachi; E Nanba
Journal:  Intern Med       Date:  2000-07       Impact factor: 1.271

7.  Two deletion mutations in the hydroxymethylbilane synthase gene in two unrelated Japanese patients with acute intermittent porphyria.

Authors:  N Maeda; Y Horie; K Adachi; E Nanba; H Kawasaki; M Daimon; Y Kudo; M Kondo
Journal:  J Hum Genet       Date:  2000       Impact factor: 3.172

8.  GM1-gangliosidosis (genetic beta-galactosidase deficiency): identification of four mutations in different clinical phenotypes among Japanese patients.

Authors:  J Nishimoto; E Nanba; K Inui; S Okada; K Suzuki
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025

Review 9.  Prediction of deleterious nonsynonymous single-nucleotide polymorphism for human diseases.

Authors:  Jiaxin Wu; Rui Jiang
Journal:  ScientificWorldJournal       Date:  2013-01-30

10.  A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy.

Authors:  Rumiko Kato; Jun Kawamura; Hirobumi Sugawara; Norio Niikawa; Naomichi Matsumoto
Journal:  Am J Med Genet A       Date:  2004-05-15       Impact factor: 2.802

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