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Knowledge database assisted gene marker selection for chronic lymphocytic leukemia
OBJECTIVE: To investigate whether previously curated chronic lymphocytic leukemia (CLL) risk genes could be leveraged in gene marker selection for the diagnosis and prediction of CLL. METHODS: A CLL genetic database (CLL_042017) was developed through a comprehensive CLL-gene relation data analysis,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134680/ https://www.ncbi.nlm.nih.gov/pubmed/29996709 http://dx.doi.org/10.1177/0300060518783072 |
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author | Xiang, Xixi Wang, Yu-Ping Cao, Hongbao Zhang, Xi |
author_facet | Xiang, Xixi Wang, Yu-Ping Cao, Hongbao Zhang, Xi |
author_sort | Xiang, Xixi |
collection | PubMed |
description | OBJECTIVE: To investigate whether previously curated chronic lymphocytic leukemia (CLL) risk genes could be leveraged in gene marker selection for the diagnosis and prediction of CLL. METHODS: A CLL genetic database (CLL_042017) was developed through a comprehensive CLL-gene relation data analysis, in which 753 CLL target genes were curated. Expression values for these genes were used for case-control classification of four CLL datasets, with a sparse representation-based variable selection (SRVS) approach employed for feature (gene) selection. Results were compared with outcomes obtained by using analysis of variance (ANOVA)-based gene selection approaches. RESULTS: For each of the four datasets, SRVS selected a subset of genes from the 753 CLL target genes, resulting in significantly higher classification accuracy, compared with randomly selected genes (100%, 100%, 93.94%, 89.39%). The SRVS method outperformed ANOVA in terms of classification accuracy. CONCLUSION: Gene markers selected from the 753 CLL genes could enable significantly greater accuracy in the prediction of CLL. SRVS provides an effective method for gene marker selection. |
format | Online Article Text |
id | pubmed-6134680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-61346802018-09-13 Knowledge database assisted gene marker selection for chronic lymphocytic leukemia Xiang, Xixi Wang, Yu-Ping Cao, Hongbao Zhang, Xi J Int Med Res Pre-Clinical Research Reports OBJECTIVE: To investigate whether previously curated chronic lymphocytic leukemia (CLL) risk genes could be leveraged in gene marker selection for the diagnosis and prediction of CLL. METHODS: A CLL genetic database (CLL_042017) was developed through a comprehensive CLL-gene relation data analysis, in which 753 CLL target genes were curated. Expression values for these genes were used for case-control classification of four CLL datasets, with a sparse representation-based variable selection (SRVS) approach employed for feature (gene) selection. Results were compared with outcomes obtained by using analysis of variance (ANOVA)-based gene selection approaches. RESULTS: For each of the four datasets, SRVS selected a subset of genes from the 753 CLL target genes, resulting in significantly higher classification accuracy, compared with randomly selected genes (100%, 100%, 93.94%, 89.39%). The SRVS method outperformed ANOVA in terms of classification accuracy. CONCLUSION: Gene markers selected from the 753 CLL genes could enable significantly greater accuracy in the prediction of CLL. SRVS provides an effective method for gene marker selection. SAGE Publications 2018-07-12 2018-08 /pmc/articles/PMC6134680/ /pubmed/29996709 http://dx.doi.org/10.1177/0300060518783072 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Pre-Clinical Research Reports Xiang, Xixi Wang, Yu-Ping Cao, Hongbao Zhang, Xi Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title | Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title_full | Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title_fullStr | Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title_full_unstemmed | Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title_short | Knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
title_sort | knowledge database assisted gene marker selection for chronic lymphocytic leukemia |
topic | Pre-Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134680/ https://www.ncbi.nlm.nih.gov/pubmed/29996709 http://dx.doi.org/10.1177/0300060518783072 |
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