Compositions and methods for performing methylation detection assays
US-2016168643-A1 · Jun 16, 2016 · US
US9632093B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9632093-B2 |
| Application number | US-201615197105-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 29, 2016 |
| Priority date | Feb 15, 2008 |
| Publication date | Apr 25, 2017 |
| Grant date | Apr 25, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
This document relates to methods and materials for detecting premalignant and malignant neoplasms. For example, methods and materials for determining whether or not a stool sample from a mammal contains nucleic acid markers or polypeptide markers of a neoplasm are provided.
Opening claim text (preview).
What is claimed is: 1. A method for characterizing a biological sample comprising: (a) obtaining a biological sample from a human individual; (b) measuring a K-ras mutation score within the obtained biological sample through exposing a portion of the biological sample to one or more K-ras specific primers and determining the K-ras mutation score by performing a digital melt curve analysis or quantitative allele-specific PCR, wherein the K-ras specific primers comprise a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 2, 3, 4, 5, 6, 7 and 8; (c) measuring a methylation level of a CpG site for BMP3 in a portion of the obtained biological sample through treating genomic DNA in the biological sample with bisulfite; amplifying the bisulfite-treated genomic DNA using primers specific for BMP3, and determining the methylation level of the CpG site by methylation-specific PCR, quantitative methylation-specific PCR, methylation-sensitive DNA restriction enzyme analysis, quantitative bisulfite pyrosequencing, or bisulfite genomic sequencing PCR; (d) comparing the K-ras mutation score and the BMP3 methylation level to a corresponding set of control samples without colorectal cancer; and (e) determining that the individual has colorectal cancer when 1) the measured K-ras mutation score is higher than in the control sample, and 2) the measured BMP3 methylation level is higher than in the control sample. 2. The method of claim 1 , wherein the biological sample is a stool sample, a tissue sample, a blood sample, or a urine sample.
acting on alpha -1, 4-glucosidic bonds, e.g. hyaluronidase, invertase, amylase · CPC title
for cancer (immunoassay for cancer G01N33/575) · CPC title
Chemical aspects of mass spectrometric analysis of biological material · CPC title
Pancreatic endopeptidase E (3.4.21.70) · CPC title
Expression markers · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.