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通过特征选择和多核学习改善多形性胶质母细胞瘤预后预测

Improve Glioblastoma Multiforme Prognosis Prediction by Using Feature Selection and Multiple Kernel Learning.

作者信息

Zhang Ya, Li Ao, Peng Chen, Wang Minghui

出版信息

IEEE/ACM Trans Comput Biol Bioinform. 2016 Sep-Oct;13(5):825-835. doi: 10.1109/TCBB.2016.2551745. Epub 2016 Apr 7.

Abstract

Glioblastoma multiforme (GBM) is a highly aggressive type of brain cancer with very low median survival. In order to predict the patient's prognosis, researchers have proposed rules to classify different glioma cancer cell subtypes. However, survival time of different subtypes of GBM is often various due to different individual basis. Recent development in gene testing has evolved classic subtype rules to more specific classification rules based on single biomolecular features. These classification methods are proven to perform better than traditional simple rules in GBM prognosis prediction. However, the real power behind the massive data is still under covered. We believe a combined prediction model based on more than one data type could perform better, which will contribute further to clinical treatment of GBM. The Cancer Genome Atlas (TCGA) database provides huge dataset with various data types of many cancers that enables us to inspect this aggressive cancer in a new way. In this research, we have improved GBM prognosis prediction accuracy further by taking advantage of the minimum redundancy feature selection method (mRMR) and Multiple Kernel Machine (MKL) learning method. Our goal is to establish an integrated model which could predict GBM prognosis with high accuracy.

摘要

多形性胶质母细胞瘤(GBM)是一种极具侵袭性的脑癌,中位生存期很短。为了预测患者的预后,研究人员提出了对不同胶质瘤癌细胞亚型进行分类的规则。然而,由于个体差异,不同亚型的GBM的生存时间往往各不相同。基因检测的最新进展已将经典的亚型规则演变为基于单一生物分子特征的更具体的分类规则。这些分类方法在GBM预后预测中被证明比传统的简单规则表现更好。然而,海量数据背后的真正力量仍未被发掘。我们相信基于多种数据类型的联合预测模型可能会表现得更好,这将进一步有助于GBM的临床治疗。癌症基因组图谱(TCGA)数据库提供了包含多种癌症的各种数据类型的庞大数据集,使我们能够以一种新的方式研究这种侵袭性癌症。在本研究中,我们利用最小冗余特征选择方法(mRMR)和多核机器(MKL)学习方法进一步提高了GBM预后预测的准确性。我们的目标是建立一个能够高精度预测GBM预后的综合模型。

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