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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 prediction of fetal monogenic genetic variations using maternal serum dna
Sk Telecom Co., Ltd.
July 13, 2017 - N°20170198348

The present invention provides a method for non-invasively detecting, expecting, or diagnosing fetal single nucleotide polymorphisms and the resultant monogenic disorders, through maternal cell-free dna sequencing. The diagnosis method according to the present invention does not harm mothers or fetuses and is convenient, in that analysis is possible using maternal blood samples; and can be favorably used for a prenatal ...
Method of double allele specific pcr for snp microarray
Phalanx Biotech Group, Inc.
June 29, 2017 - N°20170183729

The present invention provides a method of double allele specific polymerase chain reaction (pcr) for single nucleotide polymorphism (snp) microarray, the method provides the allele specific site as the 3′ teiiiiinal nucleotide of forward and reverse primers, it does not require a primer having specific nucleotides. The method of the present invention is easily to design the primer based on ...
Diagnosis and prediction of austism spectral disorder
Lineagen, Inc.
June 22, 2017 - N°20170175189

Methods and compositions for the detection of single nucleotide polymorphisms (snp) to determine whether the subject has autism spectrum disorder (asd), is likely to develop asd, or to classify a subject as having a particular asd subtype. The presence and/or absence of the one or more snps is compared to the presence and/or absence of the snps in ...
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Methods of using single nucleotide polymorphisms in the tl1a gene to predict or diagnose ...
Cedars-sinai Medical Center
June 15, 2017 - N°20170166967

This invention provides methods of diagnosing or predicting susceptibility to inflammatory bowel disease by determining the presence or absence of genetic variants in the tl1a gene. In one embodiment, a method of the invention is practiced by determining the presence or absence of tl1a production following fc-gamma-r activation. In another embodiment, the invention provides methods of treatment of ...
Canine autoimmune conditions and diagnosis and treatment thereof
The Translational Genomics Research Institute
June 15, 2017 - N°20170166964

The disclosure includes methods of identifying a dog at risk of developing a an autoimmune disease or condition, for example a hypothyroid disease or condition, comprising testing whether the dog exhibits one or more selected single nucleotide polymorphisms (snps), together with diagnostic kits for carrying out such methods, methods of treatment or prophylaxis of such autoimmune disease or condition, e. ...
Amplified isothermal detection of polynucleotides with atp release
The Board Of Trustees Of The Leland Stanford Junior University
June 08, 2017 - N°20170159112

The presence of a target polynucleotide sequence of interest, including targets comprising genetic variations or a single nucleotide polymorphism, is detected by a dna polymerization reaction, where the reaction mixture includes mixtures of nucleotides including at least one chimeric nucleoside tetraphosphate dimer atp-linked nucleotide (arn), in which atp is the leaving group. Dna synthesis with arns is shown to be ...
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Genetic markers for myb28
Plant Bioscience Limited
May 18, 2017 - N°20170137897

The present invention relates to a method for determining the genotype of a cruciferous vegetable plant for a plant with an increased glucosinolate level, comprising obtaining a sample of nucleic acids from said plant or a portion thereof and detecting in said nucleic acids a polymorphism at the myb28 locus that is genetically linked to an increased glucosinolate level. The ...
Oligonucleotides and methods for detecting kras and pik3ca mutations
Siemens Healthcare Diagnostics Inc.
May 18, 2017 - N°20170137894

Provided are oligonucleotides that are capable of detecting kras and pik3ca mutations in both cancer patients and healthy individuals with high specificity in kpcr assays. When the oligonucleotides are used as forward primers in conjunction with a defined genotyping algorithm spreadsheet, the primers are capable of enhancing detection of kras codon 12, 13, and 61 and pik3ca codon 542, 545, and 1047 single nucleotide ...
Strategies for high throughput identification and detection of polymorphisms
Keygene N.v.
May 18, 2017 - N°20170137872

The invention relates to a method for the high throughput identification of single nucleotide polymorphisms by performing a complexity reduction on two or more samples to yield two or more libraries, sequencing at least part of the libraries, aligning the identified sequences and determining any putative single nucleotide polymorphisms, confirming any putative single nucleotide polymorphism, generating detection probes for the ...
Compositions, methods, and systems for inferring bovine breed
Branhaven Llc
April 06, 2017 - N°20170096716

Provided herein are methods to discover and use single nucleotide polymorphisms (snp) for identifying breed, or line and breed, or line composition of a bovine subject. The present invention further provides specific nucleic acid sequences, snps, and snp patterns that can be used for identifying breed or breed combinations for angus, holstein, limousin, brahman, hereford, simmental, gelbvieh, charolais and beefmaster ...
Multivalent probes having single nucleotide resolution
Nanostring Technologies, Inc.
March 23, 2017 - N°20170081713

The present invention relates to, among other things, polymer strands, probes, compositions, methods, and kits for enabling accurate and robust enzyme- and amplification-free detection of dna and rna with single base resolution (e. G., detection of a single nucleotide polymorphism (snp), an insertion, and a deletion). The compositions, methods, and kits may further provide simultaneous detection of dna and/or ...
Methods of diagnosing increased risk of developing mrsa
William Beaumont Hospital
March 23, 2017 - N°20170081708

A method for diagnosing increased risk of developing methicillin-resistant staphylococcus aureus (mrsa) hospital-acquired (ha-mrsa) or community-acquired mrsa (ca-mrsa) which includes obtaining a biological sample from a subject, detecting in the sample a single nucleotide polymorphism (snp) in the fam129b gene at position 17 of seq id no 1, and comparing the nucleotide at position 17 of seq id no. 1 in the sample ...
Melting curve analysis using pna probe, method and kit for analyzing nucleotide polymorphism using melting ...
Panagene Inc.
March 09, 2017 - N°20170067092

Provided are a pna probe for detecting nucleotide polymorphism of a target gene, a melting curve analysis method for detecting the nucleotide polymorphism of the target gene using the same, a nucleotide polymorphism analysis method of a target gene including the melting curve analysis method, and a kit for detecting the nucleotide polymorphism of the target gene containing the pna ...
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Detection of nucleic acid reactions on bead arrays
Illumina, Inc
February 23, 2017 - N°20170051340

The present invention is directed to methods and compositions for the use of microsphere arrays to detect and quantify a number of nucleic acid reactions. The invention finds use in genotyping, i. E. The determination of the sequence of nucleic acids, particularly alterations such as nucleotide substitutions (mismatches) and single nucleotide polymorphisms (snps). Similarly, the invention finds use in the ...
Determining prostate cancer recurrence using polymorphisms in angiogenesis-related genes
H. Lee Moffitt Cancer Center And Research Institute, Inc.
February 02, 2017 - N°20170029902

In particular, disclosed is a method for treating a patient with prostate cancer that involves genotyping a nucleic acid sample from the subject for one or more single nucleotide polymorphism (snp) alleles in one or more genes angiogenesis, comparing the one or more snp alleles to control allele frequencies to produce a snp signature, and analyzing the snp signature to ...
Methods for assessing risk of alzheimer's disease in a patient
Wisconsin Alumni Research Foundation
January 19, 2017 - N°20170016072

Disclosed are methods for diagnosis or prognosis of alzheimer's disease in a patient. The methods may include assessing whether a patient has alzheimer's disease or assessing a patient's risk for developing alzheimer's disease. The methods typically include determining, either directly or indirectly, whether the patient has mutations, such as single nucleotide polymorphisms, in a plurality of genes that encode gene ...
Single nucleotide polymorphisms (snp) and association with resistance to immune tolerance induction
University Of Tennessee Research Foundation
January 19, 2017 - N°20170016068

This application discloses methods, systems and kits for correlating the presence or absence of certain nucleic acid sequences within a population with the ability to create immune tolerance in that same population. Tolerance can be induced by solo or repeated administration of antigen, including soluble antigens administered either intravenously or sublingually. This application also discloses methods for detecting variants. In ...
Compositions and methods for identifying altered effectiveness of beta blocker therapy
Duke University
January 05, 2017 - N°20170002417

The present invention provides a method of identifying a human subject as having an increased risk of altered effectiveness of beta blocker therapy, comprising detecting in the subject one or more single nucleotide polymorphism associated with increased risk of altered effectiveness of beta blocker therapy.
Serotonin transporter gene and treatment of alcoholism
University Of Virginia Patent Foundation
December 29, 2016 - N°20160376658

The gene responsible for encoding sert has a functional polymorphism at the 5′-regulatory promoter region, which results in two forms, long (l) and short (s). The ll-genotype is hypothesized to play a key role in the early onset of alcohol use. The present invention discloses the differences in treatment and diagnosis based on the l or short genotypes as ...
Single nucleotide polymorphism in hla-b*15:02 and use thereof
Millennium Health, Llc
December 29, 2016 - N°20160376656

Disclosed herein is a novel single nucleotide polymorphism (snp) in hla-b*15:02 that can be used as a biomarker for carbamazepine-induced severe adverse skin reactions in asians. Also provided herein are methods and reagents for assessing the specific snp, and applying the snp in predicting an increased risk of carbamazepine-induced severe adverse skin reactions.
Quantitative analysis method using microorganism 16s rdna gene having single nucleotide polymorphism
Korea Research Institute Of Standards And Science
December 29, 2016 - N°20160376638

The present invention relates to utilization of an artificially synthesized nucleic acid, and more particularly, to a quantitative analysis method capable of quantitatively adjusting gene-based microbial community analysis results by preparing a microorganism 16s rdna gene, which has a single nucleotide polymorphism (snp) at a particular location so as to be differentiated from a gene of a target microorganism on ...
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