Literature DB >> 23095910

Use of whole exome and genome sequencing in the identification of genetic causes of primary immunodeficiencies.

Janet Chou1, Toshiro K Ohsumi, Raif S Geha.   

Abstract

PURPOSE OF REVIEW: This review discusses the strengths and challenges of using whole genome sequencing (WGS)/whole exome sequencing (WES) for identifying novel genetic causes of primary immunodeficiencies. RECENT
FINDINGS: WGS permits comprehensive sequencing of introns and exons, whereas WES allows deeper sequencing of exonic regions at a lower cost. Due to the large number of genetic variants found in each genome, it is necessary to use filtering approaches to distinguish deleterious from benign variants. WES has been used successfully to identify novel genetic causes of primary immunodeficiency. Complex structural variations and non-Mendelian disorders remain challenges for WGS/WES.
SUMMARY: WGS/WES is a powerful screening tool with great potential to identify genetic causes of primary immunodeficiencies for research and clinical applications. To use WGS/WES effectively, it is necessary to understand how to filter the sequencing data and to realize its limitations as well as its strengths.

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Year:  2012        PMID: 23095910     DOI: 10.1097/ACI.0b013e3283588ca6

Source DB:  PubMed          Journal:  Curr Opin Allergy Clin Immunol        ISSN: 1473-6322


  24 in total

1.  A Novel Mutation in CD40LG Gene Causing X-Linked Hyper IgM Syndrome.

Authors:  Hyung Young Kim; Tae Min Um; Hee Ju Park
Journal:  Indian J Pediatr       Date:  2017-12-15       Impact factor: 1.967

Review 2.  Use of Genetic Testing for Primary Immunodeficiency Patients.

Authors:  Jennifer R Heimall; David Hagin; Joud Hajjar; Sarah E Henrickson; Hillary S Hernandez-Trujillo; Yuval Tan; Lisa Kobrynski; Kenneth Paris; Troy R Torgerson; James W Verbsky; Richard L Wasserman; Elena W Y Hsieh; Jack J Blessing; Janet S Chou; Monica G Lawrence; Rebecca A Marsh; Sergio D Rosenzweig; Jordan S Orange; Roshini S Abraham
Journal:  J Clin Immunol       Date:  2018-04-19       Impact factor: 8.317

Review 3.  Overview of high throughput sequencing technologies to elucidate molecular pathways in cardiovascular diseases.

Authors:  Jared M Churko; Gary L Mantalas; Michael P Snyder; Joseph C Wu
Journal:  Circ Res       Date:  2013-06-07       Impact factor: 17.367

4.  Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis.

Authors:  Sandra Ammann; Kai Lehmberg; Udo Zur Stadt; Christian Klemann; Sebastian F N Bode; Carsten Speckmann; Gritta Janka; Katharina Wustrau; Mirzokhid Rakhmanov; Ilka Fuchs; Hans C Hennies; Stephan Ehl
Journal:  J Clin Immunol       Date:  2017-09-21       Impact factor: 8.317

Review 5.  Gene hunting in the genomic era: approaches to diagnostic dilemmas in patients with primary immunodeficiencies.

Authors:  Craig Platt; Raif S Geha; Janet Chou
Journal:  J Allergy Clin Immunol       Date:  2013-10-05       Impact factor: 10.793

Review 6.  Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection.

Authors:  Nassima Fodil; David Langlais; Philippe Gros
Journal:  Trends Immunol       Date:  2016-01-12       Impact factor: 16.687

7.  Rapid Flow cytometric prenatal diagnosis of primary immunodeficiency (PID) disorders.

Authors:  Anju Mishra; Maya Gupta; Aparna Dalvi; Kanjaksha Ghosh; Manisha Madkaikar
Journal:  J Clin Immunol       Date:  2014-02-18       Impact factor: 8.317

8.  Utility of next generation sequencing in clinical primary immunodeficiencies.

Authors:  Nikita Raje; Sarah Soden; Douglas Swanson; Christina E Ciaccio; Stephen F Kingsmore; Darrell L Dinwiddie
Journal:  Curr Allergy Asthma Rep       Date:  2014-10       Impact factor: 4.919

9.  Primary Immunodeficiencies in India: Molecular Diagnosis and the Role of Next-Generation Sequencing.

Authors:  Arun Kumar Arunachalam; Madhavi Maddali; Fouzia N Aboobacker; Anu Korula; Biju George; Vikram Mathews; Eunice Sindhuvi Edison
Journal:  J Clin Immunol       Date:  2020-11-23       Impact factor: 8.317

Review 10.  Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency.

Authors:  Emily S J Edwards; Julian J Bosco; Samar Ojaimi; Robyn E O'Hehir; Menno C van Zelm
Journal:  Cell Mol Immunol       Date:  2020-08-17       Impact factor: 11.530

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