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公开(公告)号:WO2012162267A3
公开(公告)日:2014-05-15
申请号:PCT/US2012038894
申请日:2012-05-21
Applicant: FLUIDIGM CORP , ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , JONES ROBERT C , KAPER FIONA , LEBOFSKY RONALD , MAY ANDREW
Inventor: ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , JONES ROBERT C , KAPER FIONA , LEBOFSKY RONALD , MAY ANDREW
CPC classification number: C12Q1/6855 , C12N15/10 , C12N15/1065 , C12N15/65 , C12N15/66 , C12Q1/686 , C12Q1/6874
Abstract: Described herein are methods useful for incorporating one or more adaptors and/or nucleotide tag(s) and/or barcode nucleotide sequence(s) one, or typically more, target nucleotide sequences. In particular embodiments, nucleic acid fragments having adaptors, e.g., suitable for use in high-throughput DNA sequencing are generated. In other embodiments, information about a reaction mixture is encoded into a reaction product. Also described herein are methods and kits useful for amplifying one or more target nucleic acids in preparation for applications such as bidirectional nucleic acid sequencing. In particular embodiments, methods of the invention entail additionally carrying out bidirectional DNA sequencing. Also described herein are methods for encoding and detecting and/or quantifying alleles by primer extension.
Abstract translation: 本文所描述的方法可用于掺入一个或多个衔接子和/或核苷酸标签和/或条形码核苷酸序列,一个或多个靶核苷酸序列。 在具体实施方案中,产生具有适配器(例如适合用于高通量DNA测序)的核酸片段。 在其它实施方案中,关于反应混合物的信息被编码成反应产物。 本文还描述了可用于扩增一种或多种靶核酸以准备应用如双向核酸测序的方法和试剂盒。 在具体实施方案中,本发明的方法还需要进行双向DNA测序。 本文还描述了通过引物延伸来编码和检测和/或定量等位基因的方法。
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公开(公告)号:WO2012162267A2
公开(公告)日:2012-11-29
申请号:PCT/US2012/038894
申请日:2012-05-21
Applicant: FLUIDIGM CORPORATION , ANDERSON, Megan , CHEN, Peilin , FOWLER, Brian , JONES, Robert C. , KAPER, Fiona , LEBOFSKY, Ronald , MAY, Andrew
Inventor: ANDERSON, Megan , CHEN, Peilin , FOWLER, Brian , JONES, Robert C. , KAPER, Fiona , LEBOFSKY, Ronald , MAY, Andrew
CPC classification number: C12Q1/6855 , C12N15/10 , C12N15/1065 , C12N15/65 , C12N15/66 , C12Q1/686 , C12Q1/6874
Abstract: Described herein are methods useful for incorporating one or more adaptors and/or nucleotide tag(s) and/or barcode nucleotide sequence(s) one, or typically more, target nucleotide sequences. In particular embodiments, nucleic acid fragments having adaptors, e.g., suitable for use in high-throughput DNA sequencing are generated. In other embodiments, information about a reaction mixture is encoded into a reaction product. Also described herein are methods and kits useful for amplifying one or more target nucleic acids in preparation for applications such as bidirectional nucleic acid sequencing. In particular embodiments, methods of the invention entail additionally carrying out bidirectional DNA sequencing. Also described herein are methods for encoding and detecting and/or quantifying alleles by primer extension.
Abstract translation: 本文所描述的方法可用于掺入一个或多个衔接子和/或核苷酸标签和/或条形码核苷酸序列,一个或多个靶核苷酸序列。 在具体实施方案中,产生具有适配器(例如适合用于高通量DNA测序)的核酸片段。 在其它实施方案中,关于反应混合物的信息被编码成反应产物。 本文还描述了可用于扩增一种或多种靶核酸以准备应用如双向核酸测序的方法和试剂盒。 在具体实施方案中,本发明的方法还需要进行双向DNA测序。 本文还描述了通过引物延伸来编码和检测和/或定量等位基因的方法。
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公开(公告)号:WO2013177206A3
公开(公告)日:2014-01-30
申请号:PCT/US2013042086
申请日:2013-05-21
Applicant: FLUIDIGM CORP , ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , KAPER FIONA , LEBOFSKY RONALD , MAY ANDREW
Inventor: ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , KAPER FIONA , LEBOFSKY RONALD , MAY ANDREW
IPC: C12Q1/68
CPC classification number: C12Q1/6813 , B01D15/08 , C12Q1/6806 , C12Q2563/159 , C12Q2563/179 , C12Q2565/629
Abstract: In certain embodiments, the invention provides methods and devices for assaying single particles in a population of particles, wherein at least two parameters are measured for each particle. One or more parameters can be measured while the particles are in the separate reaction volumes. Alternatively or in addition, one or more parameters can be measured in a later analytic step, e.g., where reactions are carried out in the separate reaction volumes and the reaction products are recovered and analyzed. In particular embodiments, one or more parameter measurements are carried out "in parallel," i.e., essentially simultaneously in the separate reaction volumes.
Abstract translation: 在某些实施方案中,本发明提供了用于测定颗粒群体中的单个颗粒的方法和装置,其中针对每个颗粒测量至少两个参数。 当颗粒处于分开的反应体积中时,可以测量一个或多个参数。 或者或另外,可以在稍后的分析步骤中测量一个或多个参数,例如其中在分开的反应体积中进行反应并回收和分析反应产物。 在具体实施方案中,一个或多个参数测量“并行地进行”,即基本上同时在单独的反应体积中进行。
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公开(公告)号:WO2013177206A2
公开(公告)日:2013-11-28
申请号:PCT/US2013/042086
申请日:2013-05-21
Applicant: FLUIDIGM CORPORATION , ANDERSON, Megan , CHEN, Peilin , FOWLER, Brian , KAPER, Fiona , LEBOFSKY, Ronald , MAY, Andrew
Inventor: ANDERSON, Megan , CHEN, Peilin , FOWLER, Brian , KAPER, Fiona , LEBOFSKY, Ronald , MAY, Andrew
IPC: C12Q1/68
CPC classification number: C12Q1/6813 , B01D15/08 , C12Q1/6806 , C12Q2563/159 , C12Q2563/179 , C12Q2565/629
Abstract: In certain embodiments, the invention provides methods and devices for assaying single particles in a population of particles, wherein at least two parameters are measured for each particle. One or more parameters can be measured while the particles are in the separate reaction volumes. Alternatively or in addition, one or more parameters can be measured in a later analytic step, e.g., where reactions are carried out in the separate reaction volumes and the reaction products are recovered and analyzed. In particular embodiments, one or more parameter measurements are carried out "in parallel," i.e., essentially simultaneously in the separate reaction volumes.
Abstract translation: 在某些实施方案中,本发明提供用于测定颗粒群体中的单个颗粒的方法和装置,其中针对每个颗粒测量至少两个参数。 当颗粒处于分开的反应体积中时,可以测量一个或多个参数。 或者或另外,可以在稍后的分析步骤中测量一个或多个参数,例如其中在分开的反应体积中进行反应并回收和分析反应产物。 在具体实施方案中,“并行地”执行一个或多个参数测量,即基本上同时在单独的反应体积中进行。
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公开(公告)号:WO2008028931A1
公开(公告)日:2008-03-13
申请号:PCT/EP2007/059299
申请日:2007-09-05
Applicant: INSTITUT PASTEUR , GENOMIC VISION , LEBOFSKY, Ronald , BENSIMON, Aaron , WALRAFEN, Pierre
Inventor: LEBOFSKY, Ronald , BENSIMON, Aaron , WALRAFEN, Pierre
IPC: C12Q1/68
CPC classification number: C12Q1/6841 , Y10T436/143333
Abstract: The present invention relates to a method of detection of the presence of at least one domain of interest on a macromolecule to t est, wherein said method comprises the following steps: a) determining beforehand at least two target regions on the domain of interest, designing and obtaining corresponding labeled probes of each target region, named set of probe of the domain of interest, the position of these probes one compared to the others being chosen and forming the specific signature of said domain of interest on the macromolecule to test; b) after spreading of the macromolecule to test on which the probes obtained in step a) are bound, detection of the position one compared to the others of the probes bound on the linearized macromolecule, the detection of the signature of a domain of interest indicating the presence of said domain of interest on the macromolecule to test, and conversely the absence of detection of signature or part of signature of a domain of interest indicating the absence of said domain or part of said domain of interest on the macromolecule to test.
Abstract translation: 本发明涉及一种在大分子上检测至少一个感兴趣的结构域的方法,其中所述方法包括以下步骤:a)预先确定感兴趣域上的至少两个目标区域,设计 并获得每个目标区域的相应的标记探针,命名的感兴趣区域的探针组,这些探针的位置与选择的其它探针相比较,并形成所述大分子上所述感兴趣区域的特异性标记进行测试; b)在扩散大分子以测试在步骤a)中获得的探针结合后,检测与结合在线性化大分子上的探针中的其它位置相比较的位置,检测到感兴趣区域的签名 所述大分子上的所述感兴趣区域的存在进行测试,反之则不存在感兴趣区域的签名或部分签名的一部分,表明在大分子上不存在所述结构域或所述感兴趣区域的部分以进行测试。
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