通过微阵列和 RNA-seq 数据为头颈癌开发可靠的预测模型。

Chanchala D Kaddi, Wallace H Coulter, May D Wang
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摘要

进一步了解头颈部鳞状细胞癌(HNSCC)的转录组模式有助于更早诊断和更好的治疗效果。有必要整合来自多项研究的知识,以确定基本、一致的基因表达特征,从而将 HNSCC 患者样本与无病样本区分开来,尤其是在早期病理阶段检测 HNSCC。本研究利用特征整合和异质集合建模技术开发了稳健的模型,用于预测微阵列和 RNAseq 数据集中的 HNSCC 疾病状态。几个备选模型表现出良好的性能,MCC 和 AUC 值均超过 0.8。这些模型还被用于区分早期病理阶段的 HNSCC 和正常 RNA-seq 样本,结果令人鼓舞。预测建模工作流程被整合到一个具有图形用户界面的软件工具中。该工具使 HNSCC 研究人员在研究新的 HNSCC 基因表达数据集时,能利用经常观察到的转录组特征和以前开发的模型组合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Developing Robust Predictive Models for Head and Neck Cancer across Microarray and RNA-seq Data.

Increased understanding of the transcriptomic patterns underlying head and neck squamous cell carcinoma (HNSCC) can facilitate earlier diagnosis and better treatment outcomes. Integrating knowledge from multiple studies is necessary to identify fundamental, consistent gene expression signatures that distinguish HNSCC patient samples from disease-free samples, and particularly for detecting HNSCC at an early pathological stage. This study utilizes feature integration and heterogeneous ensemble modeling techniques to develop robust models for predicting HNSCC disease status in both microarray and RNAseq datasets. Several alternative models demonstrated good performance, with MCC and AUC values exceeding 0.8. These models were also applied to discriminate between early pathological stage HNSCC and normal RNA-seq samples, showing encouraging results. The predictive modeling workflow was integrated into a software tool with a graphical user interface. This tool enables HNSCC researchers to harness frequently observed transcriptomic features and ensembles of previously developed models when investigating new HNSCC gene expression datasets.

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