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首页> 外文期刊>IEEE/ACM transactions on computational biology and bioinformatics >Novel Consensus Gene Selection Criteria for Distributed GPU Partial Least Squares-Based Gene Microarray Analysis in Diffused Large B Cell Lymphoma (DLBCL) and Related Findings
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Novel Consensus Gene Selection Criteria for Distributed GPU Partial Least Squares-Based Gene Microarray Analysis in Diffused Large B Cell Lymphoma (DLBCL) and Related Findings

机译:弥散性大B细胞淋巴瘤(DLBCL)中分布式GPU局部最小二乘为基础的基因芯片分析的新型共识基因选择标准

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摘要

This paper proposes a novel consensus gene selection criteria for partial least squares-based gene microarray analysis. By quantifying the extent of consistency and distinctiveness of the differential gene expressions across different double cross validations (CV) or randomizations in terms of occurrence and randomizationp-values, the proposed criteria are able to identify a more comprehensive genes associated with the underlying disease. A Distributed GPU implementation has been proposed to accelerate the gene selection problem and about 8-11 times speed up has been achieved based on the microarray datasets considered. Simulation results using various cancer gene microarray datasets show that the proposed approach is able to achieve highly comparable classification accuracy in comparing with many conventional approaches. Furthermore, enrichment analysis on the selected genes for Diffused Large B Cell Lymphoma (DLBCL) and Prostate Cancer datasets and show that only the proposed approach is able to identify gene lists enriched in different pathways with significantp-values. In contrast, sufficient statistical significance cannot be found for conventional SVM-RFE and thet-test. The reliability in identifying and establishing statistical significance of the gene findings makes the proposed approach an attractive alternative for cancer related researches based on gene expression profiling or other similar data.
机译:本文提出了一种新的共识基因选择标准,用于基于最小二乘法的基因微阵列分析。通过量化不同的双交叉验证(CV)或随机出现和随机化方面差异基因表达的一致性和独特性程度 n p n值,建议的标准能够识别更全面的相关基因与潜在的疾病。已经提出了分布式GPU实施方案来加速基因选择问题,并且基于所考虑的微阵列数据集,已经实现了约8-11倍的加速。使用各种癌症基因微阵列数据集的模拟结果表明,与许多常规方法相比,该方法能够实现高度可比的分类精度。此外,对扩散的大B细胞淋巴瘤(DLBCL)和前列腺癌数据集的选定基因进行的富集分析表明,只有提出的方法才能够识别在不同途径中富集的基因列表,且具有明显的 n <斜体xmlns:mml =” http://www.w3.org/1998/Math/MathML “ xmlns:xlink = ” http://www.w3.org/1999/xlink “> p n值。相反,对于常规SVM-RFE和 n <斜体xmlns:mml =“ http://www.w3.org/1998/Math/MathML ” xmlns:xlink =“ http ://www.w3.org/1999/xlink “> t n-test。鉴定和建立基因发现的统计意义的可靠性使所提出的方法成为基于基因表达谱或其他类似数据的癌症相关研究的有吸引力的替代方法。

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