Daniel Pinkel - Walnut Creek CA Donna G. Albertson - Lafayette CA Joe W. Gray - San Francisco CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12Q 168 G01N 33574 G01N 3353 A01N 5508
US Classification:
435 6
Abstract:
The present invention relates to DNA sequences from regions of copy number change on chromosome 20. The sequences can be used in hybridization methods for the identification of chromosomal abnormalities associated with various diseases.
Daniel Pinkel - Walnut Creek CA Joe W. Gray - San Francisco CA Anne Kallioniemi - Rockville MD Frederic Waldman - San Francisco CA Masaru Sakamoto - Tokyo, JP
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12Q 168
US Classification:
435 6, 435 712, 536 231, 536 243
Abstract:
Disclosed are new methods comprising the use of in situ hybridization to detect abnormal nucleic acid sequence copy numbers in one or more genomes wherein repetitive sequences that bind to multiple loci in a reference chromosome spread are either substantially removed and/or their hybridization signals suppressed. The invention termed Comparative Genomic Hybridization (CGH) provides for methods of determining the relative number of copies of nucleic acid sequences in one or more subject genomes or portions thereof (for example, a tumor cell) as a function of the location of those sequences in a reference genome (for example, a normal human genome). The intensity(ies) of the signals from each labeled subject nucleic acid and/or the differences in the ratios between different signals from the labeled subject nucleic acid sequences are compared to determine the relative copy numbers of the nucleic acid sequences in the one or more subject genomes as a function of position along the reference chromosome spread. Amplifications, duplications and/or deletions in the subject genome(s) can be detected. Also provided is a method of determining the absolute copy numbers of substantially all RNA or DNA sequences in subject cell(s) or cell population(s).
High Density Array Fabrication And Readout Method For A Fiber Optic Biosensor
Daniel Pinkel - Walnut Creek CA Joe Gray - San Francisco CA Donna G. Albertson - Lafayette CA
Assignee:
The Regents of the University of California - Oakland CA Medical Research Council - London
International Classification:
C25D 1300
US Classification:
250216, 25022711, 204603, 600473
Abstract:
The invention relates to the fabrication and use of biosensors comprising a plurality of optical fibers each fiber having attached to its âsensor endâ biological âbinding partnersâ (molecules that specifically bind other molecules to form a binding complex such as antibody-antigen, lectin-carbohydrate, nucleic acid-nucleic acid, biotin-avidin, etc. ). The biosensor preferably bears two or more different species of biological binding partner. The sensor is fabricated by providing a plurality of groups of optical fibers. Each group is treated as a batch to attach a different species of biological binding partner to the sensor ends of the fibers comprising that bundle. Each fiber, or group of fibers within a bundle, may be uniquely identified so that the fibers, or group of fibers, when later combined in an array of different fibers, can be discretely addressed. Fibers or groups of fibers are then selected and discretely separated from different bundles. The discretely separated fibers are then combined at their sensor ends to produce a high density sensor array of fibers capable of assaying simultaneously the binding of components of a test sample to the various binding partners on the different fibers of the sensor array.
Comparative Fluorescence Hybridization To Oligonucleotide Microarrays
Joe Gray - San Francisco CA Dan Pinkel - Walnut Creek CA Donna Albertson - Lafayette CA Colin Collins - San Rafael CA Russell Baldocchi - San Francisco CA
Assignee:
The Regents of the University of California - Oakland CA
The present invention provides methods of determining relative copy number of target nucleic acid sequences and precise mapping of chromosomal abnormalities associated with disease. The methods of the invention use target nucleic acid sequences immobilized on a solid surface, to which a sample comprising two sets of differentially labeled nucleic acid sequences are hybridized. The hybridization of the labeled nucleic acid sequences to the solid surface is then detected using standard techniques.
Laleh Shayesteh - Foster City CA Joe W. Gray - San Francisco CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
C12Q 168
US Classification:
435 6
Abstract:
The present invention provides new probes for the detection of chromosomal alterations associated with cancer, particularly ovarian cancer. The probes bind selectively with target nucleic acid sequences at 3q26.
Laleh Shayesteh - Foster City CA Joe W. Gray - San Francisco CA
Assignee:
The Regents of the University of California - Oakland CA
International Classification:
G01N 3353
US Classification:
435 71, 435 72, 530350, 5303871
Abstract:
The present invention provides new probes for the detection of chromosomal alterations associated with cancer, particularly ovarian cancer. The probes bind selectively with target nucleic acid sequences at 3 26.
Comparative Fluorescence Hybridization To Nucleic Acid Arrays
Daniel Pinkel - Walnut Creek CA Donna Albertson - Cambridge, GB Joe W. Gray - San Francisco CA
Assignee:
The Regents of the University of California - Oakland CA Medical Research Council - London
International Classification:
C12Q 168
US Classification:
435 6, 435 5, 435 911, 435 912, 536 243
Abstract:
The present invention provides methods of determining relative copy number of target nucleic acids and precise mapping of chromosomal abnormalities associated with disease. The methods of the invention use target nucleic acids immobilized on a solid surface, to which a sample comprising two sets of differentially labeled nucleic acids are hybridized. The hybridization of the labeled nucleic acids to the solid surface is then detected using standard techniques.
The invention provides methods and devices for detecting the presence of one or more target analytes in a sample employing a channel having affixed therein one or more binding partners for each target analyte. Assays are carried out by transporting the sample through the channel to each successive binding partner so that target analyte present in said sample binds to the corresponding binding partner. The sample is then transported beyond the binding partner(s), followed by detection of any target analyte bound to each binding partner. In one embodiment, binding efficiency is increased by the use of segmented transport, wherein a first bolus or bubble of a fluid that is immiscible with the sample precedes the sample during transport and a second bolus or bubble of a fluid that is immiscible with the sample follows the sample. Many configurations are possible for the device of the invention. A preferred device includes: a substrate with a channel formed in its surface, and a cover element that overlies and seals the channel.
Name / Title
Company / Classification
Phones & Addresses
Joe Gray Life Sciences Division Director
United States Dept of Energy Noncommercial Research Organizations
1 Cyclotron Rd, Berkeley, CA 94720
Joe Gray Founder
Graychip Inc. Religious Organizations
2314 Ramona St., Palo Alto, CA 94301
Joe Gray President
Hines Nurseries Inc Flowers, Nursery Stock, and Florists' Supplies
Po Box 1449, Vacaville, CA 95696 Website: hineshort.com
Joe Gray lives right next door to this home on Leitchfield Road. He was standing in the back yard when he says a school bus came crashing through this face and into this house. He says the bus then bounced off the house, and crashed back into it, finally stopped by this porch.
Date: Apr 11, 2016
Category: U.S.
Source: Google
College Football Picks: Week 14 Predictions for Every Game
an Jose State (3-8, 2-5 Mountain West) is on a five-game losing streak, having scored only seven total points in the last two games. The Spartans' offense fell apart when quarterback Joe Gray got injured in a shutout home loss to Hawaii two weeks ago, and without him there aren't many other options.
Date: Nov 26, 2014
Category: Sports
Source: Google
Artis-Payne, Gus Bus roll as Auburn defeats San Jose State 59-13
Trovan Reed made his first career interception off of San Jose State back up quarterback Joe Gray after switching from receiver to defensive back this offseason. Jermaine Whitehead also became the first Auburn player since 2007 to record and interception in consecutive games.
Jurich completed 16 of 27 passes for 218 yards with one touchdown and two interceptions. Joe Gray took over at quarterback with about 10 minutes remaining and had a pass intercepted near the goal line late in the game.
Thirty-year-old Joe Gray captured the men's race Saturday after finishing second last year. Twenty-eight-year-old Shannon Payne took the women's field in her inaugural run up the Northeast's highest peak.
The men's and women's division winners this year hail from Colorado Springs, Colorado. Joe Gray captured the men's race, his first time breaking the tape after a second-place finish last year. Shannon Payne took the women's field.
I think everyone is pulling for him, said Joe Gray, a 59-year-old Colts season ticket holder who was impressed by the standing ovation Manning got when he returned to Lucas Oil Stadium in October. Im not saying I dont like Luck, I just wish Peyton was still here.
The idea behind the test is to take advantage of what is known about disease symptoms to narrow the search for genetic aberrations. And that, said Dr. Joe Gray, an expert in genome analysis at Oregon Health and Science University, is a good step in the right direction.