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High throughput single molecule approaches for phased genome sequence assembly

High throughput single molecule approaches for phased genome sequence assembly
用于定相基因组序列组装的高通量单分子方法
批准号:
10190986
负责人:
Pui-Yan KWOK
金额:
$65.0万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-27 至 2024-03-31

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中文摘要
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Project Summary/Abstract It is possible to combine technologies based on single molecules to achieve de novo genome sequence assembly with phasing and genome-wide structural variation identification. De novo assembled whole genome sequencing fully describes the diploid human genome except for a small number of long, highly repetitive sequences such as the centromeres, telomeres, and near-identical segmental duplications. Key to the success of phased genome sequence assembly is the single molecule mapping approach originally developed by our group and is now improved by Bionano Genomics. The method starts with sequence-specific labeling of long (180 kb to >1 Mb), double-stranded genomic DNA fragments with fluorophores followed by high- throughput, automated imaging and analysis of the linearized fluorescent DNA molecules in nanochannel arrays on a commercially available instrument. During the next phase of this project, we propose to produce phased genome sequence assemblies of 2 individuals from each of all 26 ethnic groups of the 1000 Genomes Project to serve as general references for the community. In addition, we will further develop the single molecule labeling technology to map repetitive elements that are difficult to interrogate genome-wide and to precisely phase long- range target regions. The approach we are taking to construct de novo phased and assembled genomes will produce “near reference grade” genomes with high efficiency and at low cost for many ethnic groups around the world. These reference sequences will increase substantially the value of all the whole genome sequences already obtained and provide further insight into structural variation patterns across human populations. The technology development aims of this proposal will address some of the most difficult questions facing genome analysis today. At the end of this four-year project, a robust method for phased genome assembly, repetitive sequence mapping, and long-range phasing will be developed and ready for application in many areas of genome research.
期刊论文(23)
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科研奖励(0)
会议论文
DOI: 10.1038/nmeth.3865
发表时间: 2016-07
期刊: Nature methods
影响因子: 48
作者: [Mostovoy Y, Levy-Sakin M, Lam J, Lam ET, Hastie AR, Marks P, Lee J, Chu C, Lin C, Džakula Ž, Cao H, Schlebusch SA, Giorda K, Schnall-Levin M, Wall JD, Kwok PY]
通讯作者: Kwok PY
Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis.
三名纯合子家族性高胆固醇血症患者:基因组测序和亲属分析。
DOI: 10.1002/mgg3.1007
发表时间: 2019
期刊: Molecular genetics & genomic medicine
影响因子: 2
作者: [Wong,KarenHY, Levy-Sakin,Michal, Ma,Walfred, Gonzaludo,Nina, Mak,AngelCY, Vaka,Dedeepya, Poon,Annie, Chu,Catherine, Lao,Richard, Balamir,Melek, Grenville,Zoe, Wong,Nicolas, Kane,JohnP, Kwok,Pui-Yan, Malloy,MaryJ, Pullinger,CliveR]
通讯作者: Pullinger,CliveR
DOI: 10.1038/s41467-018-05513-w
发表时间: 2018-08-02
期刊: Nature communications
影响因子: 16.6
作者: [Wong KHY, Levy-Sakin M, Kwok PY]
通讯作者: Kwok PY
DOI: 10.1534/genetics.115.183483
发表时间: 2016-01
期刊: Genetics
影响因子: 3.3
作者: [Mak AC, Lai YY, Lam ET, Kwok TP, Leung AK, Poon A, Mostovoy Y, Hastie AR, Stedman W, Anantharaman T, Andrews W, Zhou X, Pang AW, Dai H, Chu C, Lin C, Wu JJ, Li CM, Li JW, Yim AK, Chan S, Sibert J, Džakula Ž, Cao H, Yiu SM, Chan TF, Yip KY, Xiao M, Kwok PY]
通讯作者: Kwok PY
18
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