COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing (Q34109720)

31 July 2017

title

COLD-PCR enrichment of rare cancer mutations prior to targeted amplicon resequencing (English)

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31 July 2017

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John Quackenbush

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author name string

Coren A Milbury

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31 July 2017

Mick Correll

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31 July 2017

Renee Rubio

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31 July 2017

G Mike Makrigiorgos

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31 July 2017

language of work or name

English

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publication date

21 December 2011

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31 July 2017

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31 July 2017

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31 July 2017

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31 July 2017

page(s)

580-589

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Comprehensive next-generation cancer genome sequencing in the era of targeted therapy and personalized oncology

31 July 2017

cites work

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5 July 2018

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COLD-PCR: improving the sensitivity of molecular diagnostics assays

5 July 2018

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Clinical cancer genomics: how soon is now?

5 July 2018

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Ice-COLD-PCR enables rapid amplification and robust enrichment for low-abundance unknown DNA mutations

5 July 2018

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Increased sensitivity of KRAS mutation detection by high-resolution melting analysis of COLD-PCR products

5 July 2018

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5 July 2018

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The mutation spectrum revealed by paired genome sequences from a lung cancer patient

5 July 2018

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5 July 2018

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Heteroplasmic mitochondrial DNA mutations in normal and tumour cells

5 July 2018

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Ultra deep sequencing detects a low rate of mosaic mutations in tuberous sclerosis complex

5 July 2018

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5 July 2018

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COLD-PCR-enhanced high-resolution melting enables rapid and selective identification of low-level unknown mutations

5 July 2018

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Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

5 July 2018

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Two-round coamplification at lower denaturation temperature-PCR (COLD-PCR)-based sanger sequencing identifies a novel spectrum of low-level mutations in lung adenocarcinoma

5 July 2018

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Improved base calling for the Illumina Genome Analyzer using machine learning strategies

5 July 2018

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The Sequence Alignment/Map format and SAMtools

5 July 2018

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Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

5 July 2018

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Quantification of rare allelic variants from pooled genomic DNA

5 July 2018

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Coamplification at lower denaturation temperature-PCR increases mutation-detection selectivity of TaqMan-based real-time PCR.

5 July 2018

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5 July 2018

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5 July 2018

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Circulating mutant DNA to assess tumor dynamics

5 July 2018

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5 July 2018

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Direct resequencing of the complete ERBB2 coding sequence reveals an absence of activating mutations in ERBB2 amplified breast cancer

5 July 2018

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

5 July 2018

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The consensus coding sequences of human breast and colorectal cancers

5 July 2018

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Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer

5 July 2018

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p53 mutation heterogeneity in cancer

5 July 2018

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Increased detection sensitivity for KRAS mutations enhances the prediction of anti-EGFR monoclonal antibody resistance in metastatic colorectal cancer.

5 July 2018

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Importance of c-kit mutation detection method sensitivity in prognostic analyses of t(8;21)(q22;q22) acute myeloid leukemia

28 October 2018

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Rapid and sensitive detection of KRAS mutation after fast-COLD-PCR enrichment and high-resolution melting analysis.

28 October 2018

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Multiplex Amplification Coupled with COLD-PCR and High Resolution Melting Enables Identification of Low-Abundance Mutations in Cancer Samples with Low DNA Content

28 October 2018

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Next-generation sequencing of the TET2 gene in 355 MDS and CMML patients reveals low-abundance mutant clones with early origins, but indicates no definite prognostic value

28 October 2018

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Characterization of mitochondrial DNA heteroplasmy using a parallel sequencing system.

28 October 2018

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Cancer: Genomics of metastasis

28 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418918

GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma

28 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418918

The IARC TP53 database: new online mutation analysis and recommendations to users

28 October 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3418918

Deep sequencing of a genetically heterogeneous sample: local haplotype reconstruction and read error correction

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22194627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22194627

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Impact of mutant p53 functional properties on TP53 mutation patterns and tumor phenotype: lessons from recent developments in the IARC TP53 database

1 reference

5 May 2024

https://opencitations.net/index/api/v1/citations/10.1002/HUMU.20495

Identifiers

DOI

10.1373/CLINCHEM.2011.176198

1 reference

31 July 2017

1 reference

31 July 2017

1 reference