Abstract: The present invention provides kits and methods for screening drugs and drug candidates for activity by determining the presence or absence of high integrity nucleic acid in a sample.
Abstract: The invention provides methods for detecting contamination in a PCR reaction. Methods of the invention are especially useful for detection of contamination in heterogeneous samples containing a rare nucleic acid to be detected.
Abstract: The invention provides amplification-based methods for detecting hypermethylated nucleic acid in heterogeneous biological samples, e.g., stool. A screening procedure based on the detection of hypermethylation, preferably at multiple genes, provides a means for detecting various diseases, e.g., colorectal cancer. By using chimeric primers that contain a 5′ non-specific portion, the specificity and efficiency of the nucleic acid amplification is improved. Methods of the invention are especially useful in detection of rare events in a heterogeneous sample.
Abstract: Methods are provided for detecting an alteration in a target nucleic acid. Methods of the invention are useful for detecting and identifying mutations that are indicative of disease or the predisposition for disease.
Abstract: Methods are provided for selective nucleic acid sequence detection in single base primer extension reactions of high sensitivity. These methods are useful for detecting small amounts of mutant nucleic acid in a heterogeneous biological sample. These methods are particularly useful for identifying individuals with gene mutations indicative of early colorectal cancer.
Abstract: Methods and compositions are provided for detecting the presence of nucleic acid sequence variants in a subpopulation of nucleic acid molecules in a biological sample. These methods are particularly useful for identifying individuals with mutations indicative of cancer.
Type:
Application
Filed:
February 18, 2003
Publication date:
October 30, 2003
Applicant:
Exact Sciences Corporation
Inventors:
Anthony P. Shuber, Lisa Kann, Duncan Whitney
Abstract: A slotted electrophoresis gel composition and methods of use are disclosed in the present invention. The invention also describes an apparatus that is used to produce a slotted electrophoresis gel composition.
Type:
Application
Filed:
March 1, 2002
Publication date:
September 11, 2003
Applicant:
EXACT Sciences Corporation
Inventors:
Philip W. Hammond, Christopher P. Adams, Ezra S. Abrams, T. Christian Boles
Abstract: The present invention provides methods for detecting disease by analysis of a patient sample to determine the integrity of nucleic acids in the sample.
Abstract: Methods for extracting DNA from a biological sample that result in a higher yield of target DNA than conventional methods. More particularly, methods for extracting DNA include exposing the biological sample to inhibitors of DNA degradation.
Type:
Grant
Filed:
January 24, 2000
Date of Patent:
April 22, 2003
Assignee:
Exact Sciences Corporation
Inventors:
Anthony P. Shuber, Frederick A. Huntress, Jr., James K. Moore
Abstract: Methods of the invention comprise assays for markers indicative of cancer, precancer, and other diseases or disorders. Assays of the invention are preformed on heterogeneous samples obtained from patients by non-invasive or minimally-invasive methods.
Type:
Grant
Filed:
January 10, 2001
Date of Patent:
January 7, 2003
Assignee:
Exact Sciences Corporation
Inventors:
Anthony P. Shuber, William Pierceall, Steven J. Laken
Abstract: Methods of the invention comprise assays for markers indicative of cancer, precancer, and other diseases or disorders. Assays of the invention are preformed on heterogeneous samples obtained from patients by non-invasive or minimally-invasive methods. Such assays may be employed alone or in combination with other disease screening techniques.
Abstract: Methods employing purification devices comprising an electrophoretic medium containing immobilized capture probes for the purification of DNA are disclosed.
Type:
Application
Filed:
August 24, 2001
Publication date:
November 21, 2002
Applicant:
EXACT Sciences Corporation
Inventors:
Christopher P. Adams, T. Christian Boles, Lawrence Weir, Rahul K. Dhanda, Nevin M. Summers
Abstract: Methods for detecting nucleotide deletions in biological samples are described. Methods of the invention are particulary useful for detecting deletions in regions of polynucleotide repeats. In particular, methods of the invention are useful to detect deletions at the BAT26 locus.
Abstract: Methods of the invention comprise assays for markers indicative of cancer, precancer, and other diseases or disorders. Assays of the invention are preformed on heterogeneous samples obtained from patients by non-invasive or minimally-invasive methods. Such assays may be employed alone or in combination with other disease screening techniques.
Abstract: The present invention provides rapid detection methods that detect virtually all non-viral organisms, from a broad to a narrow spectrum. More particularly, the present invention provides SRP RNA nucleic acid probes and methods of using such nucleic acid probes for the rapid, sensitive detection of non-viral organisms such as bacteria, fungi, and protozoa. Using the detection methods of the present invention, major non-viral groups such as bacterial, fungi, and protozoa, as well as specific species, can be identified in samples. In addition, kits for use in carrying out the methods of the present invention are provided.
Type:
Application
Filed:
December 19, 2001
Publication date:
September 5, 2002
Applicant:
EXACT Sciences Corporation
Inventors:
T. Christian Boles, Lawrence Weir, Benjamin B. Stone
Abstract: Methods are provided for detecting an alteration in a target nucleic acid. Methods of the invention are useful for detecting and identifying mutations that are indicative of disease or the predisposition for disease.
Abstract: The invention provides an apparatus for obtaining a stool specimen. The apparatus comprises a housing, a collection bag, a slider to close the collection bag and a draw string to move the slider. A user places the apparatus on a toilet, deposits a first stool into the collection bag, then pulls the draw string to move the slider to close the collection bag thereby allowing the user to urinate or further defecate.
Type:
Grant
Filed:
December 17, 2001
Date of Patent:
July 9, 2002
Assignee:
Exact Sciences Corporation
Inventors:
Walker M. Slaon, III, Stanley N. Lapidus
Abstract: The present invention provides methods for the preparation of stool samples to increase the yield of relevant DNA, and further provides methods for isolating and analyzing target DNA for characteristics indicative of colorectal cancer. Methods for screening patients for the presence of cancerous or pre-cancerous colorectal lesions are also provided.
Type:
Grant
Filed:
May 21, 2001
Date of Patent:
June 18, 2002
Assignee:
Exact Sciences Corporation
Inventors:
Anthony P. Shuber, Stanley N. Lapidus, Gail E. Radcliffe
Abstract: An apparatus for obtaining a stool specimen. The apparatus comprises a housing, a collection bag, a slider to close the collection bag and a draw string to move the slider. A user places the apparatus on a toilet, deposits a first stool into the collection bag, then pulls the draw string to move the slider to close the collection bag thereby allowing the user to urinate or further defecate.
Type:
Grant
Filed:
March 13, 2001
Date of Patent:
March 5, 2002
Assignee:
Exact Sciences Corporation
Inventors:
Walker M. Slaon, III, Stanley N. Lapidus
Abstract: Methods are provided for identifying nucleic acids. Methods of the invention are useful for identifying and analyzing nucleic acids, especially variants of single nucleotide polymorphisms, that are indicative of disease or the predisposition for disease.