Amplification methods to minimise sequence specific bias
    31.
    发明授权
    Amplification methods to minimise sequence specific bias 有权
    使序列特异性偏差最小化的扩增方法

    公开(公告)号:US09469872B2

    公开(公告)日:2016-10-18

    申请号:US14299269

    申请日:2014-06-09

    IPC分类号: C12P19/34 C12Q1/68 C09K3/00

    摘要: Methods for amplifying nucleic acids are provided. The methods can be used to minimize sequence specific bias caused by the preferential amplification of certain nucleic acid sequences. Methods are described which can lower the efficiency of AT rich templates relative to GC rich templates, thereby minimizing GC bias during amplification reactions with multiple templates of different sequence. The methods are suited to solid phase amplification, for example, utilizing flow cells.

    摘要翻译: 提供了扩增核酸的方法。 这些方法可以用于最小化由某些核酸序列的优先扩增引起的序列特异性偏差。 描述了可以降低AT富含模板相对于GC富集模板的效率的方法,由此使具有不同序列的多个模板的扩增反应期间的GC偏差最小化。 该方法适用于固相扩增,例如利用流动池。

    Sequencing by orthogonal synthesis
    37.
    发明授权
    Sequencing by orthogonal synthesis 有权
    通过正交合成测序

    公开(公告)号:US09193999B2

    公开(公告)日:2015-11-24

    申请号:US14314864

    申请日:2014-06-25

    申请人: ILLUMINA, INC.

    IPC分类号: C12Q1/68

    摘要: A method for sequencing includes steps of (a) providing first and second nucleic acid templates, wherein the two templates have different sequences; (b) extending a first primer bound to the first template using a first polymerase species and a first set of nucleotide analogs; (c) extending a second primer bound to the second template using a second polymerase species and a second set of nucleotide analogs, wherein the first polymerase species is different from the second polymerase species and wherein the first set of nucleotide analog is different from the second set of nucleotide analog, (d) detecting the first and second primer extension products; and (e) repeating steps (b) through (d), thereby determining the different sequences of the first and second templates.

    摘要翻译: 一种用于测序的方法包括以下步骤:(a)提供第一和第二核酸模板,其中两个模板具有不同的序列; (b)使用第一聚合酶种类和第一组核苷酸类似物扩展与第一模板结合的第一引物; (c)使用第二聚合酶种类和第二组核苷酸类似物扩展与第二模板结合的第二引物,其中第一聚合酶种类与第二聚合酶种类不同,并且其中第一组核苷酸类似物不同于第二种 一套核苷酸类似物,(d)检测第一和第二引物延伸产物; 和(e)重复步骤(b)至(d),从而确定第一和第二模板的不同序列。

    Method for sequencing a polynucleotide template
    40.
    发明授权
    Method for sequencing a polynucleotide template 有权
    多核苷酸模板测序方法

    公开(公告)号:US09017945B2

    公开(公告)日:2015-04-28

    申请号:US13556053

    申请日:2012-07-23

    IPC分类号: C12Q1/68

    CPC分类号: C12Q1/6874 C12Q2535/119

    摘要: The invention relates to methods for pairwise sequencing of a double-stranded polynucleotide template, which permit the sequential determination of nucleotide sequences in two distinct and separate regions on complementary strands of the double-stranded polynucleotide template. The two regions for sequence determination may or may not be complementary to each other.

    摘要翻译: 本发明涉及用于双链多核苷酸模板的成对测序的方法,其允许在双链多核苷酸模板的互补链上的两个不同和分离的区域中顺序测定核苷酸序列。 用于序列确定的两个区域可以彼此或可以不互补。