The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Aug. 30, 2016

Filed:

Feb. 28, 2013
Applicant:

Fluidigm Corporation, San Francisco, CA (US);

Inventors:

Brian Fowler, San Mateo, CA (US);

Jake Kimball, Oakland, CA (US);

Myo Thu Maung, Brisbane, CA (US);

Andrew May, San Francisco, CA (US);

Michael C. Norris, Mountain View, CA (US);

Dominique G. Toppani, Oakland, CA (US);

Marc A. Unger, San Mateo, CA (US);

Jing Wang, Daly City, CA (US);

Jason A. A. West, Pleasanton, CA (US);

Assignee:

Fluidigm Corporation, South San Francisco, CA (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
G01N 1/34 (2006.01); G01N 1/28 (2006.01); C12P 19/34 (2006.01); C12Q 1/68 (2006.01); G01N 15/14 (2006.01); B01L 3/00 (2006.01); B01L 7/00 (2006.01);
U.S. Cl.
CPC ...
G01N 1/28 (2013.01); B01L 3/502761 (2013.01); C12P 19/34 (2013.01); C12Q 1/686 (2013.01); C12Q 1/6813 (2013.01); C12Q 1/6844 (2013.01); C12Q 1/6869 (2013.01); G01N 1/34 (2013.01); G01N 15/1484 (2013.01); B01L 7/52 (2013.01); B01L 2200/0668 (2013.01); B01L 2300/0864 (2013.01); B01L 2400/043 (2013.01); B01L 2400/0409 (2013.01); B01L 2400/0415 (2013.01); B01L 2400/0487 (2013.01); B01L 2400/086 (2013.01); B01L 2400/088 (2013.01);
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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