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Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples
Due to lack of normal samples in clinical diagnosis and to reduce costs, detection of small-scale mutations from tumor-only samples is required but remains relatively unexplored. We developed an algorithm (GATKcan) augmenting GATK with two statistics and machine learning to detect mutations in cance...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698426/ https://www.ncbi.nlm.nih.gov/pubmed/29162841 http://dx.doi.org/10.1038/s41598-017-14896-7 |
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author | Hsu, Yu-Chin Hsiao, Yu-Ting Kao, Tzu-Yuan Chang, Jan-Gowth Shieh, Grace S. |
author_facet | Hsu, Yu-Chin Hsiao, Yu-Ting Kao, Tzu-Yuan Chang, Jan-Gowth Shieh, Grace S. |
author_sort | Hsu, Yu-Chin |
collection | PubMed |
description | Due to lack of normal samples in clinical diagnosis and to reduce costs, detection of small-scale mutations from tumor-only samples is required but remains relatively unexplored. We developed an algorithm (GATKcan) augmenting GATK with two statistics and machine learning to detect mutations in cancer. The averaged performance of GATKcan in ten experiments outperformed GATK in detecting mutations of randomly sampled 231 from 241 TCGA endometrial tumors (EC). In external validations, GATKcan outperformed GATK in TCGA breast cancer (BC), ovarian cancer (OC) and melanoma tumors, in terms of Matthews correlation coefficient (MCC) and precision, where MCC takes both sensitivity and specificity into account. Further, GATKcan reduced high fractions of false positives detected by GATK. In mutation detection of somatic variants, classified commonly by VarScan 2 and MuTect from the called variants in BC, OC and melanoma, ranked by adjusted MCC (adjusted precision) GATKcan was the top 1, followed by MuTect, VarScan 2 and GATK. Importantly, GATKcan enables detection of mutations when alternate alleles exist in normal samples. These results suggest that GATKcan trained by a cancer is able to detect mutations in future patients with the same type of cancer and is likely applicable to other cancers with similar mutations. |
format | Online Article Text |
id | pubmed-5698426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56984262017-11-29 Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples Hsu, Yu-Chin Hsiao, Yu-Ting Kao, Tzu-Yuan Chang, Jan-Gowth Shieh, Grace S. Sci Rep Article Due to lack of normal samples in clinical diagnosis and to reduce costs, detection of small-scale mutations from tumor-only samples is required but remains relatively unexplored. We developed an algorithm (GATKcan) augmenting GATK with two statistics and machine learning to detect mutations in cancer. The averaged performance of GATKcan in ten experiments outperformed GATK in detecting mutations of randomly sampled 231 from 241 TCGA endometrial tumors (EC). In external validations, GATKcan outperformed GATK in TCGA breast cancer (BC), ovarian cancer (OC) and melanoma tumors, in terms of Matthews correlation coefficient (MCC) and precision, where MCC takes both sensitivity and specificity into account. Further, GATKcan reduced high fractions of false positives detected by GATK. In mutation detection of somatic variants, classified commonly by VarScan 2 and MuTect from the called variants in BC, OC and melanoma, ranked by adjusted MCC (adjusted precision) GATKcan was the top 1, followed by MuTect, VarScan 2 and GATK. Importantly, GATKcan enables detection of mutations when alternate alleles exist in normal samples. These results suggest that GATKcan trained by a cancer is able to detect mutations in future patients with the same type of cancer and is likely applicable to other cancers with similar mutations. Nature Publishing Group UK 2017-11-21 /pmc/articles/PMC5698426/ /pubmed/29162841 http://dx.doi.org/10.1038/s41598-017-14896-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Hsu, Yu-Chin Hsiao, Yu-Ting Kao, Tzu-Yuan Chang, Jan-Gowth Shieh, Grace S. Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title | Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title_full | Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title_fullStr | Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title_full_unstemmed | Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title_short | Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples |
title_sort | detection of somatic mutations in exome sequencing of tumor-only samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698426/ https://www.ncbi.nlm.nih.gov/pubmed/29162841 http://dx.doi.org/10.1038/s41598-017-14896-7 |
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