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中文摘要
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描述(由申请人提供):摘要全基因组扩增(WGA)技术提供了从耗尽的天然DNA扩增DNA的机会。这项技术有可能促进剩余DNA有限的分子流行病学研究的持续生产力。虽然等位基因扩增可能会出现错误,但WGA在SNP基因分型中的表现通常被报道为非常好的一致性和可重复性。然而,从口腔刷中获得的WGA DNA的质量尚未被彻底评估用于筛查突变或测序,并且已发表的报告大多涉及从其他来源提取的有限组DNA样本,并测试了非PCR基于WGA方法的保真度。这项验证性研究的目的是通过直接测序,确定在一项基于人群的研究中,通过大量WGA DNA样本检测种系突变和多态性的敏感性和特异性。我们计划对3580份用GenomePlex(R)试剂盒全基因组扩增的口腔刷DNA样本进行CDKN2A/p16基因测序,然后将测序数据与原始或天然DNA中已经获得的结果进行比较。我们努力证明我们可以使用WGA随机片段- PCR方法,利用这种资源对生殖系DNA进行几乎无限的未来研究,以调查与黑色素瘤风险和/或进展有关的假设。该研究还具有更广泛的科学相关性,因为它将为未来的流行病学调查提供有关口腔样本效用的一般知识。
英文摘要
DESCRIPTION (provided by applicant): Abstract Whole-genome amplification (WGA) technologies offer the opportunity to expand DNA from otherwise depleted native DNAs. This technique has the potential to facilitate the continued productivity of molecular epidemiological studies that have limited remaining DNA. Although allele amplification errors can occur, the performance of WGA in SNP genotyping has generally reported very good concordance and reproducibility. However the quality of WGA DNA obtained from buccal brushes has not been thoroughly evaluated for screening of mutations or sequencing, and published reports have mostly involved limited sets of DNA samples extracted from other sources and tested for the fidelity of non- PCR based WGA methods. The objective of this validation study is to determine the sensitivity and specificity of detecting germline mutations and polymorphisms in a large set of WGA DNA samples from a population-based study by direct sequencing. We plan to sequence the CDKN2A/p16 gene in 3580 DNA samples from buccal brushes that has been whole-genome amplified with the GenomePlex(R) kit, and then compare the sequencing data with those results already obtained in the original or native DNAs. We endeavor to demonstrate that we can use the WGA random fragmentation- PCR method to allow nearly unlimited future studies of germline DNA using this resource to investigate hypotheses in relation to melanoma risk and/or progression. The study also has a broader scientific relevance in that it will provide generalizable knowledge about the utility of buccal samples for future epidemiological investigations.
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Validation of the use of whole-genome amplified DNA in a population-based study
Mutational Analysis of Clonality in Multiple Primary Melanoma
Mutational Analysis of Clonality in Multiple Primary Melanoma
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