摘要
Whole-genome sequencing of matched germline and tumour pairs in a well-characterized cohort of melanoma
patients allowed investigation of associations between melanoma body site, age at melanoma onset and MC1R
variant status with overall mutation burden and specific base pair changes observed in the corresponding
melanoma. We observed statistically significant associations between mutation burden in melanoma and body
site, age at onset and MC1R genotype, for both ultraviolet radiation (UVR) signature
patients allowed investigation of associations between melanoma body site, age at melanoma onset and MC1R
variant status with overall mutation burden and specific base pair changes observed in the corresponding
melanoma. We observed statistically significant associations between mutation burden in melanoma and body
site, age at onset and MC1R genotype, for both ultraviolet radiation (UVR) signature
| 源语言 | English |
|---|---|
| 页(从-至) | 255-258 |
| 页数 | 4 |
| 期刊 | Pigment Cell and Melanoma Research |
| 卷 | 30 |
| 期 | 2 |
| DOI | |
| 出版状态 | Published - 7 3月 2017 |
联合国可持续发展目标
此成果有助于实现下列可持续发展目标:
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Good health and well being
学术指纹
探究 'Mutation load in melanoma is affected by MC1R genotype' 的科研主题。它们共同构成独一无二的学术指纹。引用此
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