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Title: Array-based detection of genetic alterations associated with disease

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.

Inventors:
; ;
Issue Date:
Research Org.:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1379191
Patent Number(s):
9753035
Application Number:
11/900,648
Assignee:
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Patent Classifications (CPCs):
Y - NEW / CROSS SECTIONAL TECHNOLOGIES Y10 - TECHNICAL SUBJECTS COVERED BY FORMER USPC Y10S - TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
G - PHYSICS G01 - MEASURING G01N - INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
DOE Contract Number:  
AC03-76SF00098
Resource Type:
Patent
Resource Relation:
Patent File Date: 2007 Sep 11
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; 60 APPLIED LIFE SCIENCES

Citation Formats

Pinkel, Daniel, Albertson, Donna G., and Gray, Joe W.. Array-based detection of genetic alterations associated with disease. United States: N. p., 2017. Web.
Pinkel, Daniel, Albertson, Donna G., & Gray, Joe W.. Array-based detection of genetic alterations associated with disease. United States.
Pinkel, Daniel, Albertson, Donna G., and Gray, Joe W.. Tue . "Array-based detection of genetic alterations associated with disease". United States. https://www.osti.gov/servlets/purl/1379191.
@article{osti_1379191,
title = {Array-based detection of genetic alterations associated with disease},
author = {Pinkel, Daniel and Albertson, Donna G. and Gray, Joe W.},
abstractNote = {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.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {2017},
month = {9}
}

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Works referenced in this record:

Molecular heterogeneity at the breakpoints of smaller 20q deletions
journal, September 1994


Comparative genomic hybridization of ductal carcinoma in situ of the breast—evidence of multiple genetic pathways
journal, March 1999