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公开(公告)号:EA020593B1
公开(公告)日:2014-12-30
申请号:EA201170933
申请日:2010-01-13
Applicant: FLUIDIGM CORP
Inventor: HAMILTON AMY , LIN MIN , MIR ALAIN , PIEPRZYK MARTIN
Abstract: Изобретениеотноситсяк способаманализагеномнойДНКи/илиРНКизнебольшихобразцовилидажеединичныхклеток. СпособыанализагеномнойДНКмогутвключатьполногеномнуюамплификацию (WGA) споследующейпреамплификациейи амплификациейвыбранныхнуклеиновыхкислот-мишеней. СпособыанализаРНКмогутвключатьобратнуютранскрипциюжелательнойРНКс последующейпреамплификациейи амплификациейвыбранныхнуклеиновыхкислот-мишеней.
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公开(公告)号:CA2734868A1
公开(公告)日:2010-03-11
申请号:CA2734868
申请日:2009-08-26
Applicant: FLUIDIGM CORP
Inventor: MIR ALAIN , RAMAKRISHNAN RAMESH , UNGER MARC , ZIMMERMANN BERNHARD G
Abstract: The present invention provides assay methods that increase the number of samples and/or target nucleic acids that can be analyzed in a single assay.
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公开(公告)号:EP2569453A4
公开(公告)日:2013-11-20
申请号:EP11781412
申请日:2011-05-16
Applicant: FLUIDIGM CORP
Inventor: MAY ANDREW , MIR ALAIN , RAMAKRISHNAN RAMESH , ZIMMERMANN BERNHARD
CPC classification number: C12P19/34 , C07H21/00 , C12Q1/6806 , C12Q1/6869 , C12Q2600/118 , C12Q2565/113 , C12Q2527/125 , C12Q2525/204 , C12Q2525/307 , C12Q2525/15 , C12Q2521/507
Abstract: The present invention provides methods for selectively enriching a biological sample for short nucleic acids, such as fetal DNA in a maternal sample or apoptic DNA in a biological sample from a cancer patient and for subsequently analyzing the short nucleic acids for genotype, mutation, and/or aneuploidy.
Abstract translation: 本发明提供了选择性富集生物样品的方法,所述生物样品用于短核酸,例如母体样品中的胎儿DNA或来自癌症患者的生物样品中的凋亡DNA,并随后分析短核酸的基因型,突变和/ 或非整倍体。
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公开(公告)号:EP2379753A4
公开(公告)日:2012-05-30
申请号:EP10732056
申请日:2010-01-13
Applicant: FLUIDIGM CORP
Inventor: HAMILTON AMY , LIN MIN , MIR ALAIN , PIEPRZYK MARTIN
CPC classification number: C12Q1/6881 , C12Q1/6844 , C12Q1/686 , C12Q2531/113 , C12Q2531/119 , C12Q2531/137 , C12Q2565/101 , C12Q2600/156 , C12Q2600/158 , C12Q2600/16 , C12Q2600/178
Abstract: The present invention provides methods for analysis of genomic DNA and/or RNA from small samples or even single cells. Methods for analyzing genomic DNA can entail whole genome amplification (WGA), followed by preamplification and amplification of selected target nucleic acids. Methods for analyzing RNA can entail reverse transcription of the desired RNA, followed by preamplification and amplification of selected target nucleic acids.
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公开(公告)号:SG185544A1
公开(公告)日:2012-12-28
申请号:SG2012083432
申请日:2011-05-16
Applicant: FLUIDIGM CORP
Inventor: MAY ANDREW , MIR ALAIN , RAMAKRISHNAN RAMESH , ZIMMERMANN BERNHARD
Abstract: The present invention provides methods for selectively enriching a biological sample for short nucleic acids, such as fetal DNA in a maternal sample or apoptic DNA in a biological sample from a cancer patient and for subsequently analyzing the short nucleic acids for genotype, mutation, and/or aneuploidy.
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公开(公告)号:SG183029A1
公开(公告)日:2012-08-30
申请号:SG2012052031
申请日:2010-01-13
Applicant: FLUIDIGM CORP
Inventor: HAMILTON AMY , LIN MIN , MIR ALAIN , PIEPRZYK MARTIN
Abstract: SINGLE-CELL NUCLEIC ACID ANALYSISThe present invention provides methods for analysis of genomic DNA and/or RNA from small samples or even single cells. Methods for analyzing genomic DNA can entail whole genome amplification (WGA), followed by preamplification and amplification of selected target nucleic acids. Methods for analyzing RNA can entail reverse transcription of the desired RNA, followed by preamplification and amplification of selected target nucleic acids.Fig. 1
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公开(公告)号:SG172965A1
公开(公告)日:2011-08-29
申请号:SG2011050739
申请日:2010-01-13
Applicant: FLUIDIGM CORP
Inventor: HAMILTON AMY , LIN MIN , MIR ALAIN , PIEPRZYK MARTIN
Abstract: The present invention provides methods for analysis of genomic DNA and/or RNA from small samples or even single cells. Methods for analyzing genomic DNA can entail whole genome amplification (WGA), followed by preamplification and amplification of selected target nucleic acids. Methods for analyzing RNA can entail reverse transcription of the desired RNA, followed by preamplification and amplification of selected target nucleic acids.
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