PCR-based methods for the enrichment of minority alleles and mutations (Q24657701)

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English	PCR-based methods for the enrichment of minority alleles and mutations	scientific article

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instance of

scholarly article

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review article

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stated in

Europe PubMed Central

title

PCR-based methods for the enrichment of minority alleles and mutations (English)

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author name string

Coren A Milbury

series ordinal

1

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Jin Li

series ordinal

2

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G Mike Makrigiorgos

series ordinal

3

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language of work or name

English

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publication date

April 2009

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published in

Clinical Chemistry

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volume

55

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issue

4

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page(s)

632-40

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cites work

Digital PCR

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Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

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Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing

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Combining allele-specific fluorescent probes and restriction assay in real-time PCR to achieve SNP scoring beyond allele ratios of 1:1000.

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FLAG assay as a novel method for real-time signal generation during PCR: application to detection and genotyping of KRAS codon 12 mutations

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28 September 2017

Selective amplification of rare mutations using locked nucleic acid oligonucleotides that competitively inhibit primer binding to wild-type DNA.

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28 September 2017

s-RT-MELT for rapid mutation scanning using enzymatic selection and real time DNA-melting: new potential for multiplex genetic analysis

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Detection of Ki-ras mutations in tissue and plasma samples of patients with pancreatic cancer using PNA-mediated PCR clamping and hybridisation probes

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28 September 2017

High sensitivity EndoV mutation scanning through real-time ligase proofreading

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28 September 2017

Inverse PCR-based RFLP scanning identifies low-level mutation signatures in colon cells and tumors

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Ligation of a primer at a mutation: a method to detect low level mutations in DNA.

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28 September 2017

A sensitive scanning technology for low frequency nuclear point mutations in human genomic DNA.

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28 September 2017

Restriction endonuclease-mediated selective polymerase chain reaction: a novel assay for the detection of K-ras mutations in clinical samples

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28 September 2017

A pre-Columbian Y chromosome-specific transition and its implications for human evolutionary history

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28 September 2017

Mutation detection using immobilized mismatch binding protein (MutS).

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28 September 2017

Detection of non-homology-containing heteroduplex molecules

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28 September 2017

Resolution of a missense mutant in human genomic DNA by denaturing gradient gel electrophoresis and direct sequencing using in vitro DNA amplification: HPRT Munich

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28 September 2017

Detection of single DNA base differences by competitive oligonucleotide priming

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28 September 2017

Allele-specific enzymatic amplification of beta-globin genomic DNA for diagnosis of sickle cell anemia

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28 September 2017

A novel method for detecting point mutations or polymorphisms and its application to population screening for carriers of phenylketonuria

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28 September 2017

Detection of minority point mutations by modified PCR technique: a new approach for a sensitive diagnosis of tumor-progression markers

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28 September 2017

Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide

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28 September 2017

Characterizing mutations in samples with low-level mosaicism by collection and analysis of DHPLC fractionated heteroduplexes.

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30 May 2018

Genotypic selection methods for the direct analysis of point mutations

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Restriction site mutation analysis, a proposed methodology for the detection and study of DNA base changes following mutagen exposure

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30 May 2018

Rapid and sensitive nonradioactive detection of mutant K-ras genes via 'enriched' PCR amplification

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30 May 2018

Detection of ultrarare somatic mutation in the human TP53 gene by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification

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28 November 2018

Antiprimer quenching-based real-time PCR and its application to the analysis of clinical cancer samples.

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28 November 2018

Wild-type blocking polymerase chain reaction for detection of single nucleotide minority mutations from clinical specimens.

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28 November 2018

Specific detection of bacillus anthracis using a TaqMan mismatch amplification mutation assay

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28 November 2018

Quantification of random genomic mutations.

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PubMed Central

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28 November 2018

Pyrophosphorolysis-activated polymerization (PAP): application to allele-specific amplification

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PubMed Central

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28 November 2018

Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification

1 reference

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https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous detection of multiple single-base alleles at a polymorphic site

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of K-ras mutation in sputum by mutant-allele-specific amplification (MASA)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis using the restriction site mutation (RSM) assay

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sensitive mutation detection in heterogeneous cancer specimens by massively parallel picoliter reactor sequencing

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enrichment methods for mutation detection

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19201784

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1373/CLINCHEM.2008.113035

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4514911

OpenCitations bibliographic resource ID

4514911

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4514911

PMC publication ID

2811432

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4514911

PubMed publication ID

19201784

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4514911

ResearchGate publication ID

23989229

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