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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: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:AU2003224817A1
公开(公告)日:2003-10-20
申请号:AU2003224817
申请日:2003-04-01
Applicant: FLUIDIGM CORP
Inventor: JAVADI SHERVIN , LIAU YISH-HANN , MANGER IAN D , NASSEF HANY RAMEZ , NORTON PIERCE , THRONDSET WILLIAM , CHOU HOU-PU , DARIDON ANTOINE , FARRELL KEVIN , FOWLER BRIAN , HAO CUNSHENG CASEY
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公开(公告)号:EP3140428A4
公开(公告)日:2018-02-28
申请号:EP15789313
申请日:2015-05-08
Applicant: FLUIDIGM CORP
Inventor: WEST JASON A A , FOWLER BRIAN , CHARN TZE-HOWE , JOHNSON CHRISTIAN F , UNGER MARC A
IPC: C12Q1/68
CPC classification number: C12Q1/6855 , C12N15/1065 , C12Q1/6806 , C12Q2565/501 , C12Q2521/301 , C12Q2521/501 , C12Q2525/155 , C12Q2537/162 , C12Q2565/543 , C12Q2535/122
Abstract: This disclosure provides a method of forming tagged nucleic acid sequences. A target polynucleotide is immobilized on a solid support; a recognition-oligonucleotide is hybridized thereto; the recognition-oligonucleotide-target polynucleotide hybrid is cleaved; and an adapter nucleic acid is ligated to the cleaved target polynucleotide, thereby forming a tagged nucleic acid sequence. Also provided is a method of forming a tagged single stranded cDNA; a method of forming a plurality of tagged heterogeneous nucleic acid sequences; a library of recognition-oligonucleotides; and methods for amplifying a cDNA sequence immobilized on a solid support. These methods and products can be used alone or in combination for integrated single cell sequencing, and can be adapted for use in a microfluidic apparatus or device.
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公开(公告)号:EP2376227A4
公开(公告)日:2012-07-18
申请号:EP09836688
申请日:2009-12-07
Applicant: FLUIDIGM CORP
Inventor: FOWLER BRIAN
IPC: B01L3/00
CPC classification number: B01L3/502784 , B01J2219/00286 , B01J2219/00317 , B01J2219/00398 , B01J2219/00418 , B01L7/525 , B01L2200/027 , B01L2300/0816 , B01L2300/089 , B01L2300/1805 , B01L2400/0427
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公开(公告)号:EP1499706A4
公开(公告)日:2010-11-03
申请号:EP03721509
申请日:2003-04-01
Applicant: FLUIDIGM CORP
Inventor: CHOU HOU-PU , DARIDON ANTOINE , FARRELL KEVIN , FOWLER BRIAN , HAO CUNSHENG CASEY , JAVADI SHERVIN , LIAU YISH-HANN , MANGER IAN D , NASSEF HANY RAMEZ , NORTON PIERCE , THRONDSET WILLIAM
IPC: G01N37/00 , B01L3/00 , C12M1/00 , C12M1/34 , C12M3/00 , C12N1/00 , C12Q1/02 , G01N15/02 , G01N15/14
CPC classification number: C12M1/34 , B01L3/502738 , B01L3/502746 , B01L3/502753 , B01L3/502761 , B01L2200/0636 , B01L2200/0647 , B01L2200/0652 , B01L2200/0668 , B01L2200/10 , B01L2200/12 , B01L2200/16 , B01L2300/06 , B01L2300/0636 , B01L2300/0645 , B01L2300/0681 , B01L2300/0861 , B01L2300/0867 , B01L2300/087 , B01L2300/088 , B01L2300/0887 , B01L2300/0893 , B01L2300/123 , B01L2400/0409 , B01L2400/0415 , B01L2400/0481 , B01L2400/0622 , B01L2400/0655 , C12M21/06 , C12M23/16 , G01N15/1484 , G01N33/4833 , G01N2015/008 , G01N2015/0288 , G01N2015/149 , G01N2015/1493 , G02B21/32
Abstract: The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or detection of particles, such as cells and/or beads. The invention provides systems, including apparatus, methods, and kits, for the microfluidic manipulation and/or analysis of particles, such as cells, viruses, organelles, beads, and/or vesicles. The invention also provides microfluidic mechanisms for carrying out these manipulations and analyses. These mechanisms may enable controlled input, movement/positioning, retention/localization, treatment, measurement, release, and/or output of particles. Furthermore, these mechanisms may be combined in any suitable order and/or employed for any suitable number of times within a system. Accordingly, these combinations may allow particles to be sorted, cultured, mixed, treated, and/or assayed, among others, as single particles, mixed groups of particles, arrays of particles, heterogeneous particle sets, and/or homogeneous particle sets, among others, in series and/or in parallel. In addition, these combinations may enable microfluidic systems to be reused. Furthermore, these combinations may allow the response of particles to treatment to be measured on a shorter time scale than was previously possible. Therefore, systems of the invention may allow a broad range of cell and particle assays, such as drug screens, cell characterizations, research studies, and/or clinical analyses, among others, to be scaled down to microfluidic size. Such scaled-down assays may use less sample and reagent, may be less labor intensive, and/or may be more informative than comparable macrofluidic assays.
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公开(公告)号:SG10202004286UA
公开(公告)日:2020-06-29
申请号:SG10202004286U
申请日:2015-05-08
Applicant: FLUIDIGM CORP
Inventor: WEST JASON A A , FOWLER BRIAN , CHARN TZE-HOWE , JOHNSON CHRISTIAN F , UNGER MARC A
Abstract: This disclosure provides a method of forming tagged nucleic acid sequences. A target polynucleotide is immobilized on a solid support; a recognition-oligonucleotide is hybridized thereto; the recognition-oligonucleotide-target polynucleotide hybrid is cleaved; and an adapter nucleic acid is ligated to the cleaved target polynucleotide, thereby forming a tagged nucleic acid sequence. Also provided is a method of forming a tagged single stranded cDNA; a method of forming a plurality of tagged heterogeneous nucleic acid sequences; a library of recognition-oligonucleotides; and methods for amplifying a cDNA sequence immobilized on a solid support. These methods and products can be used alone or in combination for integrated single cell sequencing, and can be adapted for use in a microfluidic apparatus or device.
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30.
公开(公告)号:SG10201608159XA
公开(公告)日:2016-11-29
申请号:SG10201608159X
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
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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