(Q24802893)

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Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping

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scholarly article

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Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping (English)

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single-nucleotide polymorphism

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based on heuristic

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whole genome sequencing

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Bryan J Barratt

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Bryan J Barratt

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Deborah J Smyth

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Neil M Walker

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12

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John A Todd

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Anne Smith

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1

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Rebecca Pask

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10

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Luc J Smink

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Alex C Lam

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Sarah Nutland

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Helen E Rance

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Rebecca C J Twells

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Rebecca C J Twells

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Meera Sebastian

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publication date

27 July 2004

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BMC Biotechnology

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4

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1

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15

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

7 April 2017

Association of the T-cell regulatory gene CTLA4 with susceptibility to autoimmune disease

1 reference

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7 April 2017

The future of genetic studies of complex human diseases

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

7 April 2017

Comprehensive human genome amplification using multiple displacement amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

7 April 2017

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Whole genome amplification: abundant supplies of DNA from precious samples or clinical specimens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Quantitative evaluation by minisequencing and microarrays reveals accurate multiplexed SNP genotyping of whole genome amplified DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Unbiased whole-genome amplification directly from clinical samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Genetic associations in large versus small studies: an empirical assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 September 2017

Parameters for reliable results in genetic association studies in common disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=514612

28 November 2018

Haplotype tagging for the identification of common disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15279678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BeadArray technology: enabling an accurate, cost-effective approach to high-throughput genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/15279678

12 December 2020

based on heuristic

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Multiple displacement amplification prior to single nucleotide polymorphism genotyping in epidemiologic studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/15279678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15279678

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1472-6750-4-15

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