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Single Nucleotide Polymorphism

Single Nucleotide Polymorphism-related patent applications - as published by the U.S. Patent and Trademark Office (USPTO).


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Method for determining p1/p2 blood type and detection kit thereof
National Taiwan University
May 17, 2018 - N°20180135125

The present invention provides a method for determining p1/p2 blood type, including steps of providing a biological sample of a subject, detecting a genotype for single nucleotide polymorphism rs2143918 or rs5751348 in a4galt gene of the biological sample and determining a phenotype of the subject based on the genotype. Further, the present invention also provides a kit for ...
Method for treating idiopathic pulmonary fibrosis
Cornell University
May 17, 2018 - N°20180133184

Aspects of the disclosure relate to a method for treating idiopathic pulmonary fibrosis (ipf) in a patient with n-acetylcysteine (nac) comprising administering nac to a patient after a sample from the patient has been genotyped and determined to be any one of: a) homozygous or heterozygous for a thymine at the single nucleotide polymorphism rs3750920; b) homozygous or cheterozygous for ...
Method for identifying variety of hop
Suntory Holdings Limited
May 03, 2018 - N°20180119234

The present invention relates to a method for identifying the variety of a hop by using an identification marker comprising at least one single nucleotide polymorphism that differs among varieties, and a method for preparing said identification marker. The present invention also provides a primer or a probe to be used in the method for identifying the variety of a ...
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Methods, tools and systems for the assessment, prevention, management and treatment selection for type 2 diabetes
Patia Biopharmia, S.a. De C.v.
April 05, 2018 - N°20180094318

The present invention provides a method of assessing type 2 diabetes susceptibility and/or predicting treatment responsiveness in a human subject, the method comprising determining the identity of at least one allele at each of three or more positions of single nucleotide polymorphism (snp) selected from the group consisting of: slc16a11—rs75493593; hnf1a—rs483353044; tcf7l2—...
Methods for detecting an increased risk for coronary heart disease
Board Of Regents, The University Of Texas System
March 22, 2018 - N°20180080083

The invention relates generally to an allele on human chromosome 9 associated with increased risk for coronary heart disease and the use or detection of such an allele in determining whether a human has an increased risk for coronary heart disease. In one aspect, the invention relates to methods for detecting a predisposition or propensity or susceptibility for coronary heart disease ...
Reusable microarray compositions and methods
Tl Biolabs Corp.
March 15, 2018 - N°20180073063

The present application provides a reusable microarray comprising a plurality of immobilized oligonucleotide probes each having one or more nucleotides that are resistant to cleavage. The microarray is useful for analyzing nucleic acids, including single nucleotide polymorphisms (snps) by extension or ligation assays.
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Methods of detecting snps related to mrsa and ssi
William Beaumont Hospital
March 01, 2018 - N°20180057881

A method for identifying, diagnosing, and treating individuals who may be at risk developing or may have developed recurrent antibiotic resistant skin infections including mrsa and ssi. Also included are methods for detecting whether a nucleotide of one or more single nucleotide polymorphisms (snp) is present at a snp position, related probes..
Treatment of cancer with inhibitors of glutaminase
March 01, 2018 - N°20180055825

The invention relates to method of treating a disease or disorder (e.g., such as cancer) in a subject, comprising administering to the subject heterocyclic compounds and pharmaceutical preparations described herein, if the subject is determined to possess at least one g allele at single nucleotide polymorphism (snp) rs6983267.. .
Nucleic acid analysis by random mixtures of non-overlapping fragments
Complete Genomic, Inc.
February 22, 2018 - N°20180051333

The invention provides methods and kits for ordering sequence information derived from one or more target polynucleotides. In one aspect, one or more tiers or levels of fragmentation and aliquoting are generated, after which sequence information is obtained from fragments in a final level or tier.
Genetic factors associated with inhibitor development in hemophilia a
January 18, 2018 - N°20180016635

The present invention provides methods for predicting the risk of an individual developing antibodies to factor viii by identifying a single nucleotide polymorphism of an immune response or immune modifier gene. The invention further provides oligonucleotides, diagnostic kits, microarrays, and isolated nucleic acids comprising single nucleotide polymorphisms of immune response or immune modifier genes..
Single nucleotide polymorphisms associated with bull fertility
Wisconsin Alumni Research Foundation
January 04, 2018 - N°20180002755

Single nucleotide polymorphic sites of the bovine map1b, ppp1r11, and ddx4 genes are associated with improved bull fertility as measured by e.g. Sire conception rates.
Rapid quantitative detection of single nucleotide polymorphisms or somatic variants and methods to identify malignant ...
The General Hospital Corporation
December 28, 2017 - N°20170369939

Provided are systems, kits, and methods for the quantitative detection of single nucleotide polymorphisms or variants to identify malignant neoplasms. The methods include use of modified oligonucleotide blockers with peptide nucleic acid backbones that hybridize to and block logarithmic amplification of the wild-type alleles of a target, and incorporation of locked nucleic acids into probes that are complementary to a ...
Nucleotide transient binding for sequencing methods
Life Technologies Corporation
December 28, 2017 - N°20170369857

Provided herein are compositions and systems for use in polymerase-dependent, nucleotide transient-binding methods. The methods are useful for deducing the sequence of a template nucleic acid molecule and single nucleotide polymorphism (snp) analyses.
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Methods for treating or preventing cancer in a kras-variant patient and for diagnosing risk of ...
Mira Dx, Inc.
December 21, 2017 - N°20170360803

The invention relates to methods for preventing cancer in a kras-variant subject which include administering to the kras-variant subject an amount of estrogen effective to reduce the risk of developing cancer. In another aspect, the invention further relates to methods for treating cancer in a kras-variant subject, which include gradually decreasing estrogen exposure in the kras-variant subject to reduce the ...
Oligonucleotide probe for detecting single nucleotide polymorphism, and method for detecting single nucleotide polymorphism
Eiken Kagaku Kabushiki Kaisha
November 30, 2017 - N°20170342471

The present invention provides an oligonucleotide probe for single nucleotide polymorphism detection to be used for a target nucleic acid where a single nucleotide polymorphism is present, the oligonucleotide probe comprising a reporter region, an anchor region, and a linker region. The reporter region comprises: an oligonucleotide consisting of a sequence perfectly matching when a nucleotide of the single nucleotide ...
Trait prediction model creation method and trait prediction method
November 23, 2017 - N°20170337483

This is a method of creating a trait prediction model for predicting a phenotype of a multifactorial trait using data of a plurality of single nucleotide polymorphisms linked to a trait for each of a plurality of individuals of an organism: representing each of the plurality of single nucleotide polymorphisms as a matrix; classifying the plurality of single nucleotide polymorphisms ...
Se33 mutations impacting genotype concordance
Life Technologies Corporation
November 23, 2017 - N°20170335377

Disclosed are primer set compositions, methods and kits for human identification using the highly complex sequence locus, se33 (actbp2) in single and multiplex pcr reactions. Additionally, disclosed are three newly discovered single nucleotide polymorphisms (snps) within the se33 locus that can cause discordance seen as mobility shift or allelic dropout.
Prediction of neonatal abstinence syndrome
Bournemouth University
November 16, 2017 - N°20170327892

A method for predicting the onset of neonatal abstinence syndrome is described. The method comprises detecting the presence or absence of two single nucleotide polymorphisms on the cyp2b6 gene.
Novel single nucleotide polymorphisms and community-associated methicillin-resistant staphylococcus aureus
November 02, 2017 - N°20170314065

The present invention is based on the discovery of novel polymorphisms (snps) in the penicillin binding protein (pbp3) gene in staphylococcus aureus. The presence of g88a and/or g2047a snps provides an accurate, reliable biomarker for the presence of methicillin resistant staphylococcus aureus (mrsa), specifically the community-associated mrsa (ca-mrsa).
Computationally efficient correlation of genetic effects with function-valued traits
Microsoft Technology Licensing, Llc
October 05, 2017 - N°20170286593

This disclosure presents a model for identifying correlations in genome-wide association studies (gwas) with function-valued traits that provides increased power and computational efficiency by use of a gaussian process regression with radial basis function (rbf) kernels to model the function-valued traits and specialized factorizations to achieve speed. A gaussian process is assigned to each partition for each allele of a ...
Single nucleotide polymorphism (snp) markers for stevia
Purecircle Usa Inc.
October 05, 2017 - N°20170283819

Stevia varieties with high a content of rebd, a high content of rebm, and a high content of rebd and rebm containing various snp markers and ugt isoforms, are disclosed. Methods of screening for the snps are also disclosed as well as for using the snps in marker assisted breeding.
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