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Patent

Process for detecting polymorphisms on the basis of nucleotide differences

TLDR
In this paper, a process for detecting polymorphisms on the basis of nucleotide differences in random segments of the nucleic acid by performing a primer extension reaction on nucleic acids and comparing the extension reaction products is described.
Abstract
A process is provided for detecting polymorphisms on the basis of nucleotide differences in random segments of the nucleic acid by performing a primer extension reaction on the nucleic acids and comparing the extension reaction products. The random nucleic acid segment can be amplified by first dissociating the extension product from the template and contacting the dissociated extension product with a primer under conditions such that an amplification extension product is synthesized using the dissociated extension product as a template. Differences in the extension product are useful as markers in constructing genetic maps and as markers to distinguish or identify individuals.

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Citations
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Sequencing of surface immobilized polymers utilizing microfluorescence detection

TL;DR: In this article, the authors used fluorescent labels in repetitive chemistry to determine terminal monomers on solid phase immobilized polymers, which are used to label polymers at defined positions on a solid substrate.
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Dna sequencing by stepwise ligation and cleavage

TL;DR: In this article, a method of nucleic acid sequence analysis based on repeated cycles of ligation to and cleavage of probes at the terminus of a target polynucleotide was proposed.
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Methods for the detection of nucleic acids

TL;DR: In this article, methods for identifying nucleic acid polymorphisms are described. But these methods are useful for identifying and analyzing nucleic acids, especially variants of single nucleotide polymorphisms, that are indicative of disease or the predisposition for disease.
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Massively parallel signature sequencing by ligation of encoded adaptors

TL;DR: In this article, a method of nucleic acid sequence analysis based on the ligation of one or more sets of encoded adaptors to the terminus of a target polynucleotide was proposed.
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Arbitrarily primed polymerase chain reaction method for fingerprinting genomes

TL;DR: The arbitrarily primed polymerase chain reaction (AP-PCR) method as discussed by the authors is suitable for the identification of bacterial species and strains, including Staphylococcus and Streptococcus species, mammals and plants.
References
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Patent

Process for amplifying nucleic acid sequences

TL;DR: In this article, a process for amplifying any desired specific nucleic acid sequence contained in a mixture of nucleic acids or mixture thereof is described, which can be repeated as often as desired.
Patent

Process for amplifying, detecting, and/or-cloning nucleic acid sequences

TL;DR: In this paper, the authors proposed a method for synthesizing nucleic acid sequences using primers, which can be repeated stepwise or simultaneously and can be replicated as often as desired.
Journal ArticleDOI

Simultaneous analysis of multiple polymorphic loci using amplified sequence polymorphisms (ASPs).

TL;DR: A systematic approach to gene mapping and genotyping based on the simultaneous analysis of multiple amplified sequence polymorphisms (ASPs), which measure variation in DNA sequences which have been amplified by a polymerase and/or a ligase is presented.
Patent

Amplification of nucleic acid sequences using random sequence oligonucleotides as primers

TL;DR: In this paper, a process for substantially amplifying template nucleic acid present in a sample is described, wherein the amplification may be performed without the need for prior knowledge of specific sequences.