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Understanding human diseases with high-throughput quantitative measurement and analysis of molecular signatures 被引量:2
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作者 YANG Li WEI Gang +2 位作者 TANG Kun NARDINI Christine han jing-dong j. 《Science China(Life Sciences)》 SCIE CAS 2013年第3期213-219,共7页
Microarray and deep sequencing technologies have provided unprecedented opportunities for mapping genome mutations,RNA transcripts,transcription factor binding,and histone modifications at high resolution at the genom... Microarray and deep sequencing technologies have provided unprecedented opportunities for mapping genome mutations,RNA transcripts,transcription factor binding,and histone modifications at high resolution at the genome-wide level.This has revolutionized the way in which transcriptomes,regulatory networks and epigenetic regulations have been studied and large amounts of heterogeneous data have been generated.Although efforts are being made to integrate these datasets unbiasedly and efficiently,how best to do this still remains a challenge.Here we review major impacts of high-throughput genome-wide data generation,their relevance to human diseases,and various bioinformatics approaches for data integration.Finally,we provide a case study on inflammatory diseases. 展开更多
关键词 GENOMICS EPIGENOMICS PHENOMICS integration data analysis
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