Annotation of the small RNA/microRNA component Drosophila genome
Annotation of the small RNA/microRNA component Drosophila genome
批准号:
7929797
负责人:
Eric C Lai
金额:
$16.89万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2011-08-31
关键词:
AllelesBiogenesisBioinformaticsCatalogingCatalogsCodeCommunitiesCultured CellsDNA Transposable ElementsDataData SetDiseaseDominant-Negative MutationDouble-Stranded RNA Binding DomainDrosophila genomeDrosophila genusDrosophila melanogasterFunctional RNAFundingGene ExpressionGene StructureGenesGenetic TranscriptionGenomeGenomicsGoalsJointsLeadLibrariesLifeMapsMediatingMessenger RNAMethodologyMethodsMicroRNAsModificationNatureNuclearOncogenesPathway interactionsPost-Transcriptional RegulationProcessProteinsRNARNA BindingRNA EditingRNA SequencesRaceReadingRegulationRibosomal RNARouteSamplingSmall Interfering RNASmall Nucleolar RNASmall RNASourceStructureTherapeutic UsesTimeTissuesTranscriptTransfer RNATransgenesTransgenic AnimalsUntranslated RNAWagesWorkbasegenome sequencingmutantnovelparent grantpri-miRNA
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Our modENCODE parent grant U01-HG004261 is aimed at annotating the functional
short regulatory RNAs of Drosophila melanogaster using deep sequencing methodology. These
include known classes of Argonaute-bound RNA such as microRNAs, small interfering RNAs,
and piRNAs. In addition, potentially novel classes of RNAs may be uncovered as a result of this
project. We request administrative supplemental funding to expand the range of our efforts to
discover and annotate novel transcripts that represent or generate short regulatory RNAs in
Drosophila. The bulk of the requested funds are dedicated to 50% salary support of a new
bioinformatician to perform essential analyses of the large amount of small RNA data that we
have produced for the consortium. We hope to uncover edited RNAs and species with
untemplated additions, and to analyze non-canonical genic sources of mi/si/piRNAs. The
remainder of the funds will be devoted towards novel methods for constructing and sequencing
libraries that are enriched for normally labile primary microRNA transcripts. Their analysis should
not only help to define microRNA gene structures, but may prove to reveal novel types of
normally labile transcripts that might escape conventional RNA-seq efforts.
U01-HG004261-03S1 Lai ARRA supplement
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