如何利用归算改进后基因组知识发现。

Muhammad Shoaib B Sehgal, Iqbal Gondal, Laurence S Dooley, Ross Coppel
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引用次数: 9

摘要

虽然微阵列使得快速研究许多复杂的生物学问题成为可能,但它们的多步骤制造在每个阶段都有出错的倾向。标准的策略是要么忽略,要么将错误的基因读数视为缺失值,尽管这种假设可以对基因选择和基因调控网络(GRN)重建等后基因组知识发现方法产生重大影响。这是一系列新的灵活的输入算法的催化剂,包括局部最小二乘输入和最近的启发式抵押品缺失值输入,它们利用功能相关基因的生物交易行为来提供准确的缺失值估计。本文研究了缺失值归算技术对基因组后知识推断方法的影响,各种算法的结果一致地证实,通过灵活和稳健的归算来回收微阵列数据,而不是忽略缺失值,可以为后续的下游程序提供实质性的性能优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How to improve postgenomic knowledge discovery using imputation.

How to improve postgenomic knowledge discovery using imputation.

How to improve postgenomic knowledge discovery using imputation.

How to improve postgenomic knowledge discovery using imputation.

While microarrays make it feasible to rapidly investigate many complex biological problems, their multistep fabrication has the proclivity for error at every stage. The standard tactic has been to either ignore or regard erroneous gene readings as missing values, though this assumption can exert a major influence upon postgenomic knowledge discovery methods like gene selection and gene regulatory network (GRN) reconstruction. This has been the catalyst for a raft of new flexible imputation algorithms including local least square impute and the recent heuristic collateral missing value imputation, which exploit the biological transactional behaviour of functionally correlated genes to afford accurate missing value estimation. This paper examines the influence of missing value imputation techniques upon postgenomic knowledge inference methods with results for various algorithms consistently corroborating that instead of ignoring missing values, recycling microarray data by flexible and robust imputation can provide substantial performance benefits for subsequent downstream procedures.

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