Experimental and bioinformatics platform for epigenome analysis using nanopore sequencing
Experimental and bioinformatics platform for epigenome analysis using nanopore sequencing
批准号:
10654043
负责人:
Kin Fai Au
金额:
$0.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-27 至 2023-07-02
关键词:
AccelerationAddressAffectAllelesBindingBiochemical ReactionBioinformaticsBiologicalBiological ProcessBiomedical ResearchCell ProliferationCell ReprogrammingCellular biologyChromatinCollaborationsComplexDNADNA MethylationDNA RepairDNA Transposable ElementsDNA biosynthesisDataData AnalysesDevelopmentEmbryonic DevelopmentEnhancersEpigenetic ProcessEventFoundationsGenesGenomeGenomic ImprintingGenomic SegmentGerm CellsHumanHuman GenomeIndividualInvestigationLaboratory ResearchLengthMethodologyMethodsMethylationModificationMusNamesNucleosomesNucleotidesPatternPhaseProtocols documentationPublicationsRegulationRepetitive SequenceResearchResolutionRoleSamplingScientistSeriesSignal TransductionSolidStructure of primordial sex cellTechniquesTechnologyTranscription ProcessUniversitiesWorkanalysis pipelinebasebisulfitechromatin immunoprecipitationcrosslinkdata formatdemethylationepigenetic regulationepigenomeexperienceexperimental studygenome integrityhuman embryonic stem cellimprintimprovedinnovationnanoporenext generation sequencingprecision medicineprototypepublic health relevancesingle moleculestem cell biologystem cellstechnique developmenttooltranscription factortranscriptome
中文摘要
项目摘要/摘要
英文摘要
PROJECT SUMMARY / ABSTRACT
The epigenetic status of genomes including nucleosome occupancy, chromatin accessibility and DNA methylation,
is highly relevant to the regulation of DNA-template biological processes from transcription to DNA replication and
repair. Most existing techniques for characterizing epigenome utilize Next Generation Sequencing (NGS)
following the biochemical reactions that capture the signals (e.g., bisulfite conversion, cross-linking and
chromatin immunoprecipitation/ChIP). The development of these techniques has dramatically accelerated the
research of different epigenetics events and has led to many important biological findings. As the new
technique nanopore sequencing has been optimized to convey robust sequencing data of single DNA
molecules with long read length, it brings in new discernible information that is useful for addressing certain
challenging but important epigenetics problems. We develop an experimental protocol MeSMLR-seq and a
series of bioinformatics methods to define the multiple types of epigenetic events, including nucleosome
occupancy, chromatin accessibility and DNA methylation, at the rarely explored genome regions and biological
context by leveraging the unique information of nanopore sequencing. Utilizing these experimental and
bioinformatics methods, we aim to interrogate the following problems during the epigenetic reprogramming of
early embryonic development and primordial germ cell development: in Aim 1, we will study the epigenetic
regulation of transposable element expression and transposition. Aim 2 will construct the allele-specific
epigenome and identify the genome loci with significant epigenome difference between alleles. Aim 3 will
identify significant difference of the epigenomes between DNA strands and investigate their regulatory roles
and dynamics during epigenetic reprogramming. These studies are anticipated to provide the first experimental
and bioinformatics platform for improve our understanding of epigenome with complex biomedical context in a
comprehensive manner.
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会议论文
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批准号:10929710
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项目类别:
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依托单位:
Experimental and bioinformatics platform for epigenome analysis using nanopore sequencing
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依托单位:
海外基金