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DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information
Identifying differentially expressed genes (DEGs) between tumor and normal samples is critical for studying tumorigenesis, and has been routinely applied to identify diagnostic, prognostic, and therapeutic biomarkers for many cancers. It is well-known that solid tumor tissue samples obtained from cl...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121016/ https://www.ncbi.nlm.nih.gov/pubmed/30210526 http://dx.doi.org/10.3389/fgene.2018.00321 |
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author | Zhang, Weiwei Long, Haixia He, Binsheng Yang, Jialiang |
author_facet | Zhang, Weiwei Long, Haixia He, Binsheng Yang, Jialiang |
author_sort | Zhang, Weiwei |
collection | PubMed |
description | Identifying differentially expressed genes (DEGs) between tumor and normal samples is critical for studying tumorigenesis, and has been routinely applied to identify diagnostic, prognostic, and therapeutic biomarkers for many cancers. It is well-known that solid tumor tissue samples obtained from clinical settings are always mixtures of cancer and normal cells. However, the tumor purity information is more or less ignored in traditional differential expression analyses, which might decrease the power of differential gene identification or even bias the results. In this paper, we have developed a novel differential gene calling method called DECtp by integrating tumor purity information into a generalized least square procedure, followed by the Wald test. We compared DECtp with popular methods like t-test and limma on nine simulation datasets with different sample sizes and noise levels. DECtp achieved the highest area under curves (AUCs) for all the comparisons, suggesting that cancer purity information is critical for DEG calling between tumor and normal samples. In addition, we applied DECtp into cancer and normal samples of 14 tumor types collected from The Cancer Genome Atlas (TCGA) and compared the DEGs with those called by limma. As a result, DECtp achieved more sensitive, consistent, and biologically meaningful results and identified a few novel DEGs for further experimental validation. |
format | Online Article Text |
id | pubmed-6121016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61210162018-09-12 DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information Zhang, Weiwei Long, Haixia He, Binsheng Yang, Jialiang Front Genet Genetics Identifying differentially expressed genes (DEGs) between tumor and normal samples is critical for studying tumorigenesis, and has been routinely applied to identify diagnostic, prognostic, and therapeutic biomarkers for many cancers. It is well-known that solid tumor tissue samples obtained from clinical settings are always mixtures of cancer and normal cells. However, the tumor purity information is more or less ignored in traditional differential expression analyses, which might decrease the power of differential gene identification or even bias the results. In this paper, we have developed a novel differential gene calling method called DECtp by integrating tumor purity information into a generalized least square procedure, followed by the Wald test. We compared DECtp with popular methods like t-test and limma on nine simulation datasets with different sample sizes and noise levels. DECtp achieved the highest area under curves (AUCs) for all the comparisons, suggesting that cancer purity information is critical for DEG calling between tumor and normal samples. In addition, we applied DECtp into cancer and normal samples of 14 tumor types collected from The Cancer Genome Atlas (TCGA) and compared the DEGs with those called by limma. As a result, DECtp achieved more sensitive, consistent, and biologically meaningful results and identified a few novel DEGs for further experimental validation. Frontiers Media S.A. 2018-08-28 /pmc/articles/PMC6121016/ /pubmed/30210526 http://dx.doi.org/10.3389/fgene.2018.00321 Text en Copyright © 2018 Zhang, Long, He and Yang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Zhang, Weiwei Long, Haixia He, Binsheng Yang, Jialiang DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title | DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title_full | DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title_fullStr | DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title_full_unstemmed | DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title_short | DECtp: Calling Differential Gene Expression Between Cancer and Normal Samples by Integrating Tumor Purity Information |
title_sort | dectp: calling differential gene expression between cancer and normal samples by integrating tumor purity information |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6121016/ https://www.ncbi.nlm.nih.gov/pubmed/30210526 http://dx.doi.org/10.3389/fgene.2018.00321 |
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