Microfluidic sample preparation for genomic sequencing of clinical pathogen isolates
Microfluidic sample preparation for genomic sequencing of clinical pathogen isolates
批准号:
9018768
负责人:
Paul Clark Blainey
金额:
$22.13万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-01-01 至 2017-12-31
关键词:
AffectAntibiotic ResistanceBacteriaBacterial GenomeBiomassCapitalCellsClinicalClinical TrialsCommunicable DiseasesConsumptionCultured CellsDNADNA Microarray ChipDNA SequenceDNA purificationDataData AnalysesData CollectionData QualityData SetDevicesDiagnosisDiseaseElementsEpidemiologyEquipmentGenomeGenomic DNAGenomicsGoalsInfection ControlInstitutesLaboratoriesLaboratory cultureLearningLibrariesMedicalMedical DeviceMedicineMicrofluidicsNational Institute of Allergy and Infectious DiseaseOutputPatientsPerformancePopulation DynamicsPreparationProceduresProcessProtocols documentationReadingReagentResearch DesignResistanceRisk FactorsSamplingScientistSequence AnalysisSpecific qualifier valueStaphylococcus aureusSurveysSystemTechnologyTestingTimeValidationWalkingbacterial resistancebaseclinical decision-makingclinical sequencingcostdesignexpectationgenome analysisgenome sequencingimprovedinstrumentmethicillin resistant Staphylococcus aureusmicro-total analysis systemmicrobialnovelpathogenpathogen genomeprototypepublic health relevanceresistance genetransmission processwhole genome
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): DNA sequencing has seen dramatic cost reductions in recent years, while sample preparation costs have been relatively flat. The result is a `sample preparation bottleneck' apparent today will affect essentially all sequencing studies within a few years. In addition, sample input quantity requirements for standard approaches exclude important low-yield clinical sample types. The goal of this R21 project is to validate and demonstrate a practical integrated microfluidic sample preparation technology for pathogen genome sequencing that enables a significant advance in sample preparation cost, turn-around-time, and low-input capability. Integration of the entire sample preparation process in a single micro device will reduce real-world cost for high-throughput sample preparation more than 10-fold by lowering reagent consumption, the need for other consumables, capital equipment costs, hands-on time, and procedural errors. We will validate this technology on S. Aureus samples from an ongoing clinical trial, Project CLEAR, and then go on to sequence a large number of additional Project CLEAR samples.
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海外基金