Next‐generation sequencing errors due to genetic variation in <i>WRAP53</i> encoding TCAB1 on chromosome 17-Reference-Cited by-同舟云学术

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Next‐generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17

Published:2022-09-24 Issue:12 Volume:43 Page:1856-1859
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Savage Sharon A.¹^ORCID,Jones Kristine²³,Teshome Kedest²³,Lori Adriana⁴,McReynolds Lisa J.¹,Niewisch Marena R.¹

Affiliation:

1. Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda Maryland USA

2. Cancer Genomics Research Laboratory, Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda Maryland USA

3. Leidos Biomedical Research, Inc. Frederick National Laboratory for Cancer Research Frederick Maryland USA

4. American Cancer Society Atlanta Georgia USA

Funder

Division of Cancer Epidemiology and Genetics, National Cancer Institute

Publisher

Hindawi Limited

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.24469

Reference13 articles.

1. Biallelic mutations in WRAP53 result in dysfunctional telomeres, Cajal bodies and DNA repair, thereby causing Hoyeraal–Hreidarsson syndrome

2. The American Cancer Society Cancer Prevention Study II Nutrition Cohort

3. Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

4. Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes

5. Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation

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