pubmed-article:15598820 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C1511726 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C0002345 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C0392747 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C0851285 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C1709016 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C0443172 | lld:lifeskim |
pubmed-article:15598820 | lifeskim:mentions | umls-concept:C0205556 | lld:lifeskim |
pubmed-article:15598820 | pubmed:issue | 22 | lld:pubmed |
pubmed-article:15598820 | pubmed:dateCreated | 2004-12-15 | lld:pubmed |
pubmed-article:15598820 | pubmed:abstractText | Alternative splicing has recently emerged as a major mechanism of regulation in the human genome, occurring in perhaps 40-60% of human genes. Thus, microarray studies of functional regulation could, in principle, be extended to detect not only the changes in the overall expression of a gene, but also changes in its splicing pattern between different tissues. However, since changes in the total expression of a gene and changes in its alternative splicing can be mixed in complex ways among a set of samples, separating these effects can be difficult, and is essential for their accurate assessment. We present a simple and general approach for distinguishing changes in alternative splicing from changes in expression, based on detecting systematic anti-correlation between the log-ratios of two different samples versus a pool containing both samples. We have tested this analysis method on microarray data for five human tissues, generated using a standard microarray platform and experimental protocols shown previously to be sensitive to alternative splicing. Our automatic analysis was able to detect a wide variety of tissue-specific alternative splicing events, such as exon skipping,mutually exclusive exons, alternative 3' and alternative 5' splicing, alternative initiation and alternative termination, all of which were validated by independent reverse-transcriptase PCR experiments, with validation rates of 70-85%. Our analysis method also enables hierarchical clustering of genes and samples by the level of similarity to their alternative splicing patterns, revealing patterns of tissue-specific regulation that are distinct from those obtained by hierarchical clustering of gene expression from the same microarray data. Our data and analysis source code are available from http://www.bioinformatics.ucla.edu/ASAP. | lld:pubmed |
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pubmed-article:15598820 | pubmed:language | eng | lld:pubmed |
pubmed-article:15598820 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15598820 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15598820 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15598820 | pubmed:issn | 1362-4962 | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:WangQiQ | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:LeeChristophe... | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:XuQiangQ | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:NelsonStanley... | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:MitsourasKath... | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:RoyMeenakshiM | lld:pubmed |
pubmed-article:15598820 | pubmed:author | pubmed-author:LeKeithK | lld:pubmed |
pubmed-article:15598820 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:15598820 | pubmed:volume | 32 | lld:pubmed |
pubmed-article:15598820 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15598820 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15598820 | pubmed:pagination | e180 | lld:pubmed |
pubmed-article:15598820 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:15598820 | pubmed:year | 2004 | lld:pubmed |
pubmed-article:15598820 | pubmed:articleTitle | Detecting tissue-specific regulation of alternative splicing as a qualitative change in microarray data. | lld:pubmed |
pubmed-article:15598820 | pubmed:affiliation | Department of Chemistry and Biochemistry, Center for Genomics and Proteomics, Molecular Biology Institute, University of California, Los Angeles, CA 90095-1570, USA. | lld:pubmed |
pubmed-article:15598820 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:15598820 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:15598820 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:15598820 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:15598820 | pubmed:publicationType | Evaluation Studies | lld:pubmed |
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