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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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Cell population analysis using single nucleotide polymorphisms from single cell transcriptomes
Fred Hutchinson Cancer Research Center
September 14, 2017 - N°20170260584

The disclosure provides methods and systems for producing single cell rna sequencing data. Single nucleotide polymorphisms (snps) identified in such data can be used to distinguish subpopulations of cells within a mixed population.
Human identification using a panel of snps
Life Technologies Corporation
September 07, 2017 - N°20170253922

The present invention provides methods, compositions, kits, systems and apparatus that are useful for multiplex pcr of one or more nucleic acids which belong to a panel of single nucleotide polymorphisms (snps) useful to identify a human. In particular, various target-specific primers are provided that allow for the selective amplification of one or more target sequences in the panel. In ...
Methods and compositions for treating a subject with a smad7 antisense oligonucleotide
Nogra Pharma Limited
August 24, 2017 - N°20170240893

The present invention relates to treatment of inflammatory bowel disease (e. G., crohn's disease and ulcerative colitis) using antisense nucleotides that are directed against polymorphic forms (e. G., those containing single nucleotide polymorphisms) of the smad7 mrna. The invention thus relates to treatment methods for subjects having polymorphic forms of smad7 and antisense oligonucleotides that specifically target smad7 mrna transcripts ...
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Site-specific endonuclease guided rolling circle amplification
Simply Diagnostics Inc.
July 27, 2017 - N°20170211137

The disclosure provides methods and kits involving site-specific endonuclease guided rolling circle amplification (rca). Nucleic acid substrates, optionally generated by hybridizing a guidance primer to a single stranded nucleic acid, are cleaved with a site-specific endonuclease. In the presence of the target site, endonuclease cleavage of the substrate generates a nucleic acid having a free 3′-hydroxyl end, which is ...
Method of characterizing sequences from genetic material samples
The Translational Genomics Research Institute
July 20, 2017 - N°20170206311

Among other aspects provided herein is a method describing the use of single nucleotide polymorphism (snp) genotyping microarrays to resolve whether genetic material (such as genomic dna) derived from a particular individual is present in a genetic material mixture (such as a complex genomic dna mixture) is disclosed. Furthermore, it is demonstrated that the identification of the presence of genetic ...
Microrna polymorphisms conferring enhanced drought tolerance in a plant
Syngenta Participations Ag
July 20, 2017 - N°20170204476

Methods of identifying a single nucleotide polymorphism associated with a plant trait and methods of identifying a plant having an improved trait. The plant trait is correlated with at least one single nucleotide polymorphism in a microrna region of a plant genome. Isolated nucleic acids, transgenic plants, and methods of producing the same are also disclosed.
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Method for predicting risk of ankylosing spondylitis using dna copy number variants
Catholic University Industry Academic Cooperation Foundation
July 20, 2017 - N°20170204463

The present invention relates to a method of predicting the risk of developing ankylosing spondylitis using dna copy number variation. It was verified that the risk of developing ankylosing spondylitis can be effectively predicted using primers for detecting dna copy number variation, of the present invention, and the sensitivity and specificity of prediction can be improved by grafting the results ...
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 ...
Analytical methods for cell free nucleic acids and applications
Centre National De La Recherche Scientifique (cnrs)
June 15, 2017 - N°20170166982

The present invention is directed to an in vitro method of detecting cell free nucleic acids, preferably cell free dna (cfdna) in a body fluid sample from an individual or a patient, wherein the method comprises the step of accurately and sensitively determining the concentration of cell free nucleic acid in the sample and/or determining the concentration or amount ...
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. ...
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Unheated extraction of genomic dna in an automated laboratory system
True Health Ip Llc
June 08, 2017 - N°20170159107

A method for analyzing genomic dna includes introducing a plurality of samples comprising human cells into individual vessels in each of a plurality of multi-vessel well plates. At least a subset of the human cells in the plurality of samples is lysed without the use of heat. Dna in the at least a subset of lysed human cells is isolated ...
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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