Knowledge database assisted gene marker selection for chronic lymphocytic leukemia

被引:1
|
作者
Xiang, Xixi [1 ]
Wang, Yu-Ping [2 ]
Cao, Hongbao [3 ,4 ]
Zhang, Xi [1 ]
机构
[1] Army Mil Med Univ, Affiliated Hosp 2, Ctr Hematol, 83 Xinqiao St, Chongqing 40037, Peoples R China
[2] Tulane Univ, Dept Biomed Engn, New Orleans, LA 70118 USA
[3] Elsevier Inc, R&D Solut, Dept Genom Res, Rockville, MD USA
[4] NIMH, Unit Stat Genom, NIH, Bethesda, MD 20892 USA
关键词
Chronic lymphocytic leukemia (CLL); sparse representation; variable selection; disease prediction; case-control classification; genetic databases; gene markers; ASSOCIATION; APOPTOSIS; CELLS;
D O I
10.1177/0300060518783072
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:3358 / 3364
页数:7
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