Whole-exome sequencing of fibroblast and its iPS cell lines derived from a patient diagnosed with xeroderma pigmentosum

Cells from a patient with a DNA repair-deficiency disorder are anticipated to bear a large number of somatic mutations. Because such mutations occur independently in each cell, there is a high degree of mosaicism in patients' tissues. While major mutations that have been expanded in many cognat...

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Bibliographic Details
Published in:Genom Data
Main Authors: Okamura, Kohji, Toyoda, Masashi, Hata, Kenichiro, Nakabayashi, Kazuhiko, Umezawa, Akihiro
Format: Artigo
Language:Inglês
Published: Elsevier 2015
Subjects:
Data in Brief
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4664661/
https://ncbi.nlm.nih.gov/pubmed/26697316
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gdata.2015.07.008
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