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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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82.
公开(公告)号:SG11201405235VA
公开(公告)日:2014-11-27
申请号:SG11201405235V
申请日:2013-02-28
Applicant: FLUIDIGM CORP
Inventor: FOWLER BRIAN , KIMBALL JAKE , MAUNG MYO THU , MAY ANDREW , NORRIS MICHAEL C , TOPPANI DOMINIQUE G , UNGER MARC A , WANG JING , WEST JASON A A
IPC: G01N15/10
Abstract: Methods, systems, and devices are described for multiple single-cell capturing and processing utilizing microfluidics. Tools and techniques are provided for capturing, partitioning, and/or manipulating individual cells from a larger population of cells along with generating genetic information and/or reactions related to each individual cell. Different capture configurations may be utilized to capture individual cells and then processing each individual cell in a multi-chamber reaction configuration. Some embodiments may provide for specific target amplification, whole genome amplification, whole transcriptome amplification, real-time PCR preparation, copy number variation, preamplification, mRNA sequencing, and/or haplotyping of the multiple individual cells that have been partitioned from the larger population of cells. Some embodiments may provide for other applications. Some embodiments may be configured for imaging the individual cells or associated reaction products as part of the processing. Reaction products may be harvested and/or further analyzed in some cases.
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公开(公告)号:SG10201404682WA
公开(公告)日:2014-10-30
申请号:SG10201404682W
申请日:2009-12-07
Applicant: FLUIDIGM CORP
Inventor: FOWLER BRIAN
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公开(公告)号:SG194745A1
公开(公告)日:2013-12-30
申请号:SG2013081195
申请日:2012-05-21
Applicant: FLUIDIGM CORP
Inventor: ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , JONES ROBERT C , KAPER FIONA , LEBOFSKY RONALD , ANDREW MAY
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.
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公开(公告)号:CA2874343A1
公开(公告)日:2013-11-28
申请号:CA2874343
申请日:2013-05-21
Applicant: FLUIDIGM CORP
Inventor: ANDERSON MEGAN , CHEN PEILIN , FOWLER BRIAN , KAPER FIONA , LEBOFSKY RONALD , MAY ANDREW
IPC: C12Q1/68
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.
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公开(公告)号:HK1170543A1
公开(公告)日:2013-03-01
申请号:HK12111058
申请日:2012-11-02
Applicant: FLUIDIGM CORP
Inventor: MAY ANDREW , CHEN PEILIN , WANG JUN , KAPER FIONA , ANDERSON MEGAN
IPC: C12Q20060101
Abstract: The present invention provides an elastomer microfluidic device that enables simultaneous amplification of multiple nucleic acid samples with multiple pairs of primers in a matrix format as well as recovery of the products e.g. for next generation sequencing. The flow of samples and reagents as well as the compartmentalization of individual reactions in the multiple channels and chambers is controlled using valves and dilation pumping / volumetric capacitive pumping.
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公开(公告)号:SG174617A1
公开(公告)日:2011-10-28
申请号:SG2011071420
申请日:2010-04-02
Applicant: FLUIDIGM CORP
Inventor: MAY ANDREW , CHEN PEILIN , WANG JUN , KAPER FIONA , ANDERSON MEGAN
Abstract: In certain embodiments, the present invention provides amplification methods in which nucleotide tag(s) and, optionally, a barcode nucleotide sequence are added to target nucleotide sequences. In other embodiments, the present invention provides a microfluidic device that includes a plurality of first input lines and a plurality of second input lines. The microfluidic device also includes a plurality of sets of first chambers and a plurality of sets of second chambers. Each set of first chambers is in fluid communication with one of the plurality of first input lines. Each set of second chambers is in fluid communication with one of the plurality of second input lines. The microfluidic device further includes a plurality of first pump elements in fluid communication with a first portion of the plurality of second input lines and a plurality of second pump elements in fluid communication with a second portion of the plurality of second input lines.
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公开(公告)号:AU2010232439A1
公开(公告)日:2011-10-27
申请号:AU2010232439
申请日:2010-04-02
Applicant: FLUIDIGM CORP
Inventor: ANDREW MAY , PEILIN CHEN , WANG JUN , FIONA KAPER , MEGAN ANDERSON
IPC: C12Q1/68
Abstract: In certain embodiments, the present invention provides amplification methods in which nucleotide tag(s) and, optionally, a barcode nucleotide sequence are added to target nucleotide sequences. In other embodiments, the present invention provides a microfluidic device that includes a plurality of first input lines and a plurality of second input lines. The microfluidic device also includes a plurality of sets of first chambers and a plurality of sets of second chambers. Each set of first chambers is in fluid communication with one of the plurality of first input lines. Each set of second chambers is in fluid communication with one of the plurality of second input lines. The microfluidic device further includes a plurality of first pump elements in fluid communication with a first portion of the plurality of second input lines and a plurality of second pump elements in fluid communication with a second portion of the plurality of second input lines.
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公开(公告)号:SG172015A1
公开(公告)日:2011-07-28
申请号:SG2011041597
申请日:2009-12-07
Applicant: FLUIDIGM CORP
Inventor: FOWLER BRIAN
Abstract: A microfluidic device includes a pressure source and a control line in fluid communication with the pressure source. The microfluidic device also includes a plurality of valves operated via the control line and an independent valve positioned adjacent the control line and between the pressure source and the plurality of valves.
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公开(公告)号:AT500051T
公开(公告)日:2011-03-15
申请号:AT02763970
申请日:2002-04-05
Applicant: FLUIDIGM CORP
Inventor: HUANG JIANG , XIAO SHOUJUN , UNGER MARC
IPC: B29C71/00 , G01N37/00 , A61L27/00 , B01J20/285 , B01L3/00 , B81B1/00 , C08F257/02 , C08F263/04 , C08F265/04 , C08F279/02 , C08F287/00 , C08F291/00 , C08J5/12 , C08J7/12 , C08K5/00 , C08L83/04 , C08L101/00 , F04B43/04 , H01J49/04
Abstract: The present invention is directed to a surface modified polymer comprising a surface which is covalently bonded to a surface modifying compound. Formation of the covalent bond between the polymer and the surface modifying compound is achieved by a reaction between an intrinsic functional group that is present in the polymer and the functional group of the surface modifying compound. By using a polymer having an intrinsic functional group, a separate surface activation step is avoided.
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