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pubmed-article:19160516pubmed:abstractTextTarget prediction for animal microRNAs (miRNAs) has been hindered by the small number of verified targets available to evaluate the accuracy of predicted miRNA-target interactions. Recently, a dataset of 3,404 miRNA-associated mRNA transcripts was identified by immunoprecipitation of the RNA-induced silencing complex components AIN-1 and AIN-2. Our analysis of this AIN-IP dataset revealed enrichment for defining characteristics of functional miRNA-target interactions, including structural accessibility of target sequences, total free energy of miRNA-target hybridization and topology of base-pairing to the 5' seed region of the miRNA. We used these enriched characteristics as the basis for a quantitative miRNA target prediction method, miRNA targets by weighting immunoprecipitation-enriched parameters (mirWIP), which optimizes sensitivity to verified miRNA-target interactions and specificity to the AIN-IP dataset. MirWIP can be used to capture all known conserved miRNA-mRNA target relationships in Caenorhabditis elegans at a lower false-positive rate than can the current standard methods.lld:pubmed
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pubmed-article:19160516pubmed:authorpubmed-author:FordF CFClld:pubmed
pubmed-article:19160516pubmed:authorpubmed-author:MeiJ LJLlld:pubmed
pubmed-article:19160516pubmed:authorpubmed-author:ZhangLiangLlld:pubmed
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pubmed-article:19160516pubmed:pagination813-9lld:pubmed
pubmed-article:19160516pubmed:dateRevised2011-7-28lld:pubmed
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pubmed-article:19160516pubmed:articleTitlemirWIP: microRNA target prediction based on microRNA-containing ribonucleoprotein-enriched transcripts.lld:pubmed
pubmed-article:19160516pubmed:affiliationProgram in Molecular Medicine, University of Massachusetts Medical School, 373 Plantation Street, Suite 306, Worcester, Massachusetts 01605, USA.lld:pubmed
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