Abstract
The exponential growth of high-throughput Omics data has provided an unprecedented opportunity for new target identification to fuel the dried-up drug discovery pipeline. However, the bioinformatics analysis of large amount and heterogeneous Omics data has posed a great deal of technical challenges for experimentalists who lack statistical skills. Moreover, due to the complexity of human diseases, it is essential to analyze the Omics data in the context of molecular networks to detect meaningful biological targets and understand disease processes. Here, we describe an integrated bioinformatics analysis strategy and provide a running example to identify suitable targets for our in-house Enzyme-Mediated Cancer Imaging and Therapy (EMCIT) technology. In addition, we go through a few key concepts in the process, including corrected false discovery rate (FDR), Gene Ontology (GO), pathway analysis, and tissue specificity. We also describe popular programs and databases which allow the convenient annotation and network analysis of Omics data. We provide a practical guideline for researchers to quickly follow the protocol described and identify those targets that are pertinent to their work.
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Acknowledgments
This work was supported in part by National Cancer Institute grant, Detection of Prostate Cancer Genomic Signatures in Blood (to AIK). Work in the Y. Yang laboratory was supported by Start-up Fund (grant: 3016-893318) at Dalian University of Technology and National Science Foundation in China, Medical Division Oncology Department (grant: 81000975).
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Yang, Y., Adelstein, S.J., Kassis, A.I. (2011). Integrated Bioinformatics Analysis for Cancer Target Identification. In: Mayer, B. (eds) Bioinformatics for Omics Data. Methods in Molecular Biology, vol 719. Humana Press. https://doi.org/10.1007/978-1-61779-027-0_25
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DOI: https://doi.org/10.1007/978-1-61779-027-0_25
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