Abstract
High-throughput array-based assays have been widely used for diagnostics and biomarker discovery. However, the development of these assays requires analysis of high-dimensional genomic data and clinical validation of the resulting models, which remain challenging. In this chapter, we describe all the steps of array-based data analysis from data quality control and normalization to higher-level analyses such as clustering, dimensionality reduction, and predictive modeling, with special emphasis on the pitfalls and dangers of such analyses. We then tackle the problems related to clinical validation of array-based biomarkers and predictive assays, which include reproducibility and portability of the initial discovery and its translation into clinics. As array-based data, and those generated by the next-generation sequencing technologies, become less expensive to produce and more widely available, the growing number of patients for whom we have genomic data will open new opportunities for development of robust and reliable genomic biomarkers—provided we apply the lessons we have learned from this last decade of array-based studies.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.