Nanopore Enabled Exonuclease Sequencing
Nanopore Enabled Exonuclease Sequencing
批准号:
9171771
负责人:
Eric Ervin
金额:
$22.5万
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:
2016-09-16 至 2018-02-28
关键词:
AddressBase SequenceBenchmarkingBindingBiologicalChemicalsCyclodextrinsDNADNA SequenceDNA Sequence AlterationDetectionDevelopmentDevicesDiscriminationEngineeringEvaluationExonucleaseFilmGeometryGlassGoalsGovernmentHealthHereditary DiseaseHumanIndividualLipid BilayersMeasurementMembraneMethodologyMethodsMolecularNatureNucleotidesOral cavityPathogen detectionPersonsPhasePolymersPore ProteinsPropertyReadingReproducibilityShapesSiliconSmall Business Innovation Research GrantSolidSpecificitySystemTemperatureTransport Processbasecostfluid flowgenome sequencinginterestnanoporenovelpersonalized medicinepressurepreventprogramsresearch studysensorsuccessvoltage
中文摘要
项目摘要
该计划的总体目标是开发一种纳米孔,使DNA单核苷酸,如那些
从核酸外切酶释放,以100%的准确度被捕获和读取,从而使
核酸外切酶/纳米孔测序概念。虽然用分子适配器进行碱基识别,
先前已经证明,以100%的效率捕获分子是目前的限制。通过
创建拟议的设备,我们将能够使用新的方法来控制分子的传输速率,
将单核苷酸盐引入并通过孔,从而实现100%的捕获效率。
英文摘要
Project Summary
The overall goal of this program is to develop a nanopore that will allow DNA mononucleotides, such as those
released from an exonuclease, to be captured and read with 100% accuracy, thus enabling the
exonuclease/nanopore-based sequencing concept. While base discrimination with a molecular adapter has
been previously demonstrated, capturing the molecules with 100% efficiency is the current limitation. By
creating the proposed device, we will be able to use novel methods to control the molecular transport rate of
the mononucleotides to and through the pore, enabling 100% capture efficiency.
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会议论文
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海外基金