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公开(公告)号:US08198027B2
公开(公告)日:2012-06-12
申请号:US11962072
申请日:2007-12-20
申请人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Norman C. Nelson , Lyle J. Arnold, Jr.
发明人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Norman C. Nelson , Lyle J. Arnold, Jr.
CPC分类号: C12Q1/6881 , C12Q1/6834 , C12Q1/6844 , C12Q1/6865 , C12Q2525/155 , C12Q2525/186 , C12Q2525/197 , C12Q2531/143 , C12Q2565/543
摘要: Compositions that are used in nucleic acid amplification in vitro are disclosed, which include a target specific universal (TSU) promoter primer or promoter provider oligonucleotide that includes a target specific (TS) sequence that hybridizes specifically to a target sequence that is amplified and a universal (U) sequence that is introduced into the sequence that is amplified, by using a primer for the universal sequence. Methods of nucleic acid amplification in vitro are disclosed that use one or more TSU oligonucleotides to attached a U sequence to a target nucleic acid in a target capture step and then use a primer for a U sequence in subsequent amplification steps performed in substantially isothermal conditions to make amplification products that contain a U sequence that indicates the presence of the target nucleic acid in a sample.
摘要翻译: 公开了用于体外核酸扩增的组合物,其包括目标特异性通用(TSU)启动子引物或启动子提供者寡核苷酸,其包括与扩增的靶序列特异性杂交的靶特异性(TS)序列和通用 (U)序列,通过使用通用序列的引物引入扩增的序列。 公开了体外核酸扩增方法,其中使用一种或多种TSU寡核苷酸将U序列连接到目标捕获步骤中的靶核酸,然后在基本上等温条件下进行的随后扩增步骤中使用U序列引物 制备含有指示样品中靶核酸存在的U序列的扩增产物。
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公开(公告)号:US08512955B2
公开(公告)日:2013-08-20
申请号:US12828676
申请日:2010-07-01
申请人: Steven T. Brentano , Dmitry Lyakhov , Norman C. Nelson , James D. Carlson , Michael M. Becker , Lyle J. Arnold, Jr.
发明人: Steven T. Brentano , Dmitry Lyakhov , Norman C. Nelson , James D. Carlson , Michael M. Becker , Lyle J. Arnold, Jr.
CPC分类号: C12Q1/6865 , C12Q1/6844 , C12Q1/6848 , C12Q1/6853 , C12Q2549/119 , C12Q2537/143 , C12Q2531/143
摘要: Compositions, reaction mixtures, and methods for performing an amplification reaction, including multiplex amplification reaction, wherein the method comprises using one or more amplification oligomer complexes comprising linked first and second amplification oligomer members. In one aspect, the amplification oligomer complex is hybridized to a target nucleic acid, the target nucleic acid with hybridized amplification oligomer complex is then captured, and other components are washed away. Target sequences of the target nucleic acids are pre-amplified to generate a first amplification product. The first amplification product is amplified in one or more secondary amplification reactions to generate second amplification products.
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公开(公告)号:US20120178636A1
公开(公告)日:2012-07-12
申请号:US13380018
申请日:2010-07-01
申请人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Michael M. Becker , Norman C. Nelson , Lyle J. Arnold, JR.
发明人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Michael M. Becker , Norman C. Nelson , Lyle J. Arnold, JR.
IPC分类号: C40B30/00
CPC分类号: C12Q1/6865 , C12Q1/6844 , C12Q1/6848 , C12Q1/6853 , C12Q2549/119 , C12Q2537/143 , C12Q2531/143
摘要: Compositions, reaction mixtures, and methods for performing an amplification reaction, including multiplex amplification reaction, wherein the method comprises using one or more amplification oligomer complexes comprising linked first and second amplification oligomer members. In one aspect, the amplification oligomer complex is hybridized to a target nucleic acid, the target nucleic acid with hybridized amplification oligomer complex is then captured, and other components are washed away. Target sequences of the target nucleic acids are pre-amplified to generate a first amplification product. The first amplification product is amplified in one or more secondary amplification reactions to generate second amplification products.
摘要翻译: 用于进行扩增反应的组合物,反应混合物和方法,包括多重扩增反应,其中所述方法包括使用包含连接的第一和第二扩增寡聚体成员的一种或多种扩增寡聚体复合物。 一方面,将扩增寡聚物复合物与靶核酸杂交,然后捕获具有杂交扩增寡聚物复合物的靶核酸,并洗涤其它组分。 靶核酸的靶序列被预扩增以产生第一扩增产物。 第一扩增产物在一个或多个二级扩增反应中扩增以产生第二扩增产物。
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公开(公告)号:US09169512B2
公开(公告)日:2015-10-27
申请号:US13380018
申请日:2010-07-01
申请人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Michael M. Becker , Norman C. Nelson , Lyle J. Arnold, Jr.
发明人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Michael M. Becker , Norman C. Nelson , Lyle J. Arnold, Jr.
CPC分类号: C12Q1/6865 , C12Q1/6844 , C12Q1/6848 , C12Q1/6853 , C12Q2549/119 , C12Q2537/143 , C12Q2531/143
摘要: Compositions, reaction mixtures, and methods for performing an amplification reaction, including multiplex amplification reaction, wherein the method comprises using one or more amplification oligomer complexes comprising linked first and second amplification oligomer members. In one aspect, the amplification oligomer complex is hybridized to a target nucleic acid, the target nucleic acid with hybridized amplification oligomer complex is then captured, and other components are washed away. Target sequences of the target nucleic acids are pre-amplified to generate a first amplification product. The first amplification product is amplified in one or more secondary amplification reactions to generate second amplification products.
摘要翻译: 用于进行扩增反应的组合物,反应混合物和方法,包括多重扩增反应,其中所述方法包括使用包含连接的第一和第二扩增寡聚体成员的一种或多种扩增寡聚体复合物。 一方面,将扩增寡聚物复合物与靶核酸杂交,然后捕获具有杂交扩增寡聚物复合物的靶核酸,并洗涤其它组分。 靶核酸的靶序列被预扩增以产生第一扩增产物。 第一扩增产物在一个或多个二级扩增反应中扩增以产生第二扩增产物。
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公开(公告)号:US08642268B2
公开(公告)日:2014-02-04
申请号:US13460341
申请日:2012-04-30
申请人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Norman C. Nelson , Lyle J. Arnold, Jr. , Michael M. Becker
发明人: Steven T. Brentano , Dmitry Lyakhov , James D. Carlson , Norman C. Nelson , Lyle J. Arnold, Jr. , Michael M. Becker
CPC分类号: C12Q1/6881 , C12Q1/6834 , C12Q1/6844 , C12Q1/6865 , C12Q2525/155 , C12Q2525/186 , C12Q2525/197 , C12Q2531/143 , C12Q2565/543
摘要: Compositions that are used in nucleic acid amplification in vitro are disclosed, which include a target specific universal (TSU) promoter primer or promoter provider oligonucleotide that includes a target specific (TS) sequence that hybridizes specifically to a target sequence that is amplified and a universal (U) sequence that is introduced into the sequence that is amplified, by using a primer for the universal sequence. Methods of nucleic acid amplification in vitro are disclosed that use one or more TSU oligonucleotides to attached a U sequence to a target nucleic acid in a target capture step and then use a primer for a U sequence in subsequent amplification steps performed in substantially isothermal conditions to make amplification products that contain a U sequence that indicates the presence of the target nucleic acid in a sample.
摘要翻译: 公开了用于体外核酸扩增的组合物,其包括目标特异性通用(TSU)启动子引物或启动子提供者寡核苷酸,其包括与扩增的靶序列特异性杂交的靶特异性(TS)序列和通用 (U)序列,通过使用通用序列的引物引入扩增的序列。 公开了体外核酸扩增方法,其中使用一种或多种TSU寡核苷酸将U序列连接到目标捕获步骤中的靶核酸,然后在基本上等温条件下进行的随后扩增步骤中使用U序列引物 制备含有指示样品中靶核酸存在的U序列的扩增产物。
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公开(公告)号:US10767208B2
公开(公告)日:2020-09-08
申请号:US14342764
申请日:2012-09-06
申请人: Norman C. Nelson , Jijumon Chelliserry , Steven T. Brentano , Dmitry Lyakhov , Matthew C. Friedenberg , Anne-Laure Shapiro
发明人: Norman C. Nelson , Jijumon Chelliserry , Steven T. Brentano , Dmitry Lyakhov , Matthew C. Friedenberg , Anne-Laure Shapiro
IPC分类号: C12Q1/68 , C12P19/34 , C12Q1/6869 , C12Q1/6855
摘要: The invention provides compositions and methods for making closed nucleic acid structures in which one or both strands are continuous. The closed nucleic acid structures can be used as sequencing templates among other applications.
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公开(公告)号:US20140329282A1
公开(公告)日:2014-11-06
申请号:US14342764
申请日:2012-09-06
申请人: Norman C. Nelson , Jijumon Chelliserry , Steven T. Brentano , Dmitry Lyakhov , Matthew C. Friedenberg , Anne-Laure Shapiro
发明人: Norman C. Nelson , Jijumon Chelliserry , Steven T. Brentano , Dmitry Lyakhov , Matthew C. Friedenberg , Anne-Laure Shapiro
IPC分类号: C12P19/34
摘要: The invention provides compositions and methods for making closed nucleic acid structures in which one or both strands are continuous. The closed nucleic acid structures can be used as sequencing templates among other applications.
摘要翻译: 本发明提供用于制备其中一条或两条链是连续的封闭核酸结构的组合物和方法。 封闭的核酸结构可以用作其他应用中的测序模板。
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公开(公告)号:US20140378318A1
公开(公告)日:2014-12-25
申请号:US14342725
申请日:2012-09-06
IPC分类号: C12Q1/68
摘要: The invention provides methods of forming a circular template for sequencing a target nucleic acid. The circular template is generated by amplification of a segment of the target nucleic acid with chimeric primers with complementary 5′ ends. The circular template has a single nick or gap providing a site for initiation of template-directed extension for sequence analysis. Sequencing of a single template generates reads of alternating segments of the same strand of the target nucleic spaced by primer segments. The different reads of the same strand of the target nucleic acid can be compiled to generate a consensus sequence. Because only one strand of the target nucleic acid is sequenced per reaction, the present method avoids errors introduced by unwittingly combining sequences of both strands of a heteroduplex PCR product. Because only one strand of the target nucleic acid is sequenced per reaction, the present method avoids errors introduced by unwittingly combining sequences of both strands of a heteroduplex PCR product.
摘要翻译: 本发明提供形成用于测序靶核酸的圆形模板的方法。 通过用具有互补的5'末端的嵌合引物扩增靶核酸的片段来产生圆形模板。 圆形模板具有单个切口或间隙,提供用于启动用于序列分析的模板指导扩展的位点。 单个模板的测序产生与引物区间隔的靶核心的相同链的交替片段的读数。 可以编译目标核酸的相同链的不同读数以产生共有序列。 因为每个反应只对靶核酸的一条链进行测序,所以本方法避免了通过不经意地组合异源双链PCR产物的两条链的序列引入的错误。 因为每个反应只对靶核酸的一条链进行测序,所以本方法避免了通过不经意地组合异源双链PCR产物的两条链的序列引入的错误。
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公开(公告)号:US10752944B2
公开(公告)日:2020-08-25
申请号:US14342725
申请日:2012-09-06
IPC分类号: C12Q1/68 , C12Q1/6869 , C12Q1/6855 , C12Q1/6844
摘要: The invention provides methods of forming a circular template for sequencing a target nucleic acid. The circular template is generated by amplification of a segment of the target nucleic acid with chimeric primers with complementary 5′ ends. The circular template has a single nick or gap providing a site for initiation of template-directed extension for sequence analysis. Sequencing of a single template generates reads of alternating segments of the same strand of the target nucleic spaced by primer segments. The different reads of the same strand of the target nucleic acid can be compiled to generate a consensus sequence. Because only one strand of the target nucleic acid is sequenced per reaction, the present method avoids errors introduced by unwittingly combining sequences of both strands of a heteroduplex PCR product. Because only one strand of the target nucleic acid is sequenced per reaction, the present method avoids errors introduced by unwittingly combining sequences of both strands of a heteroduplex PCR product.
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