Bioinformatics Analysis of Omics Data for Biomarker Identification in Clinical Research, Volume II

Bioinformatics Analysis of Omics Data for Biomarker Identification in Clinical Research, Volume II
Author :
Publisher : Frontiers Media SA
Total Pages : 757
Release :
ISBN-10 : 9782832531754
ISBN-13 : 283253175X
Rating : 4/5 (75X Downloads)

Book Synopsis Bioinformatics Analysis of Omics Data for Biomarker Identification in Clinical Research, Volume II by : Lixin Cheng

Download or read book Bioinformatics Analysis of Omics Data for Biomarker Identification in Clinical Research, Volume II written by Lixin Cheng and published by Frontiers Media SA. This book was released on 2023-09-05 with total page 757 pages. Available in PDF, EPUB and Kindle. Book excerpt: This Research Topic is part of a series with, "Bioinformatics Analysis of Omics Data for Biomarker Identification in Clinical Research - Volume I" (https://www.frontiersin.org/research-topics/13816/bioinformatics-analysis-of-omics-data-for-biomarker-identification-in-clinical-research) The advances and the decreasing cost of omics data enable profiling of disease molecular features at different levels, including bulk tissues, animal models, and single cells. Large volumes of omics data enhance the ability to search for information for preclinical study and provide the opportunity to leverage them to understand disease mechanisms, identify molecular targets for therapy, and detect biomarkers of treatment response. Identification of stable, predictive, and interpretable biomarkers is a significant step towards personalized medicine and therapy. Omics data from genomics, transcriptomics, proteomics, epigenomics, metagenomics, and metabolomics help to determine biomarkers for prognostic and diagnostic applications. Preprocessing of omics data is of vital importance as it aims to eliminate systematic experimental bias and technical variation while preserving biological variation. Dozens of normalization methods for correcting experimental variation and bias in omics data have been developed during the last two decades, while only a few consider the skewness between different sample states, such as the extensive over-repression of genes in cancers. The choice of normalization methods determines the fate of identified biomarkers or molecular signatures. From these considerations, the development of appropriate normalization methods or preprocessing strategies may promote biomarker identification and facilitate clinical decision-making.

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