| Literature DB >> 18194723 |
Abstract
Novel biomarker development requires a significant resource commitment to translate candidate markers into clinical assays. Consequently, it is imperative high quality candidates are selected early in a biomarker development program. High throughput gene expression data are routinely used to identify transcripts differentially expressed in diseased versus normal samples. Data-mining Expressed Sequence Tag, Serial Analysis of Gene Expression, Massively Parallel Signature Sequencing, and microarray expression databases can provide additional information on the expression of candidate biomarkers across multiple tissues, organs, and disease states. From this information, quantitative measures of tissue-specific gene specificity are computed and used to guide candidate biomarker selection.Entities:
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Year: 2008 PMID: 18194723 DOI: 10.1016/j.cll.2007.10.009
Source DB: PubMed Journal: Clin Lab Med ISSN: 0272-2712 Impact factor: 1.935