DOE Patents title logo U.S. Department of Energy
Office of Scientific and Technical Information

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 Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1176177
Patent Number(s):
7267947
Application Number:
10/198,805
Assignee:
The Regents of the University of California (Oakland, CA)
Patent Classifications (CPCs):
C - CHEMISTRY C12 - BIOCHEMISTRY C12Q - MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS
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: 2002 Jul 19
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., 2007. 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/1176177.
@article{osti_1176177,
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 = {2007},
month = {9}
}

Works referenced in this record:

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
journal, October 1992


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


High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays
journal, October 1998


Induction of mammary epithelial hyperplasias and mammary tumors in transgenic mice expressing a murine mammary tumor virus/activated c-src fusion gene.
journal, August 1995