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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:
; ;
Publication Date:
Research Org.:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1379191
Patent Number(s):
9,753,035
Application Number:
11/900,648
Assignee:
THE REGENTS OF THE UNIVERSITY OF CALIFORNIA LBNL
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. doi:. 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 = {Tue Sep 05 00:00:00 EDT 2017},
month = {Tue Sep 05 00:00:00 EDT 2017}
}

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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


Co-amplification of erbB2, topoisomerase II α and retinoic acid receptor α genes in breast cancer and allelic loss at topoisomerase I on chromosome 20
journal, January 1993