SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis. (Q30706997)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12140336%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

SNP genotyping on pooled DNAs: comparison of genotyping technologies and a semi automated method for data storage and analysis (English)

1 reference

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11 November 2019

1 reference

1

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11 November 2019

David J. Porteous

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11 November 2019

Peter M. Visscher

3

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Douglas H R Blackwood

1 reference

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9

Walter J Muir

1 reference

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11 November 2019

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Kathryn L Evans

1 reference

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11 November 2019

6

Stewart W Morris

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11 November 2019

4

Helen S Torrance

1 reference

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11 November 2019

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Colin A M Semple

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11 November 2019

author name string

Stéphane J Ballereau

2

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11 November 2019

Jeni Pinson

5

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11 November 2019

Marian L Thomson

7

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11 November 2019

language of work or name

English

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publication date

1 August 2002

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11 November 2019

published in

Nucleic Acids Research

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11 November 2019

volume

30

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11 November 2019

issue

15

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11 November 2019

page(s)

e74

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Accessing genetic variation: genotyping single nucleotide polymorphisms

11 November 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER)

20 June 2018

1 reference

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The effect that genotyping errors have on the robustness of common linkage-disequilibrium measures

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: practice, problems and promise

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Association study designs for complex diseases

20 June 2018

1 reference

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Precise estimation of allele frequencies of single-nucleotide polymorphisms by a quantitative SSCP analysis of pooled DNA.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Searching for genetic determinants in the new millennium

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

High-throughput SNP allele-frequency determination in pooled DNA samples by kinetic PCR.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

The impact of genotyping error on family-based analysis of quantitative traits

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

A 6.9-Mb high-resolution BAC/PAC contig of human 4p15.3-p16.1, a candidate region for bipolar affective disorder.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=137092

Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12140336

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12140336

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Determining SNP allele frequencies in DNA pools

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12140336

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GNF070

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12140336%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12140336%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12140336%20AND%20SRC:MED&resulttype=core&format=json