(Q41014616)

25 September 2017

SNP discovery in pooled samples with mismatch repair detection (English)

1 reference

25 September 2017

1 reference

Hossein Fakhrai-Rad

1

1 reference

25 September 2017

Jianbiao Zheng

2

1 reference

25 September 2017

Thomas D Willis

3

1 reference

25 September 2017

Kee Wong

4

1 reference

25 September 2017

Kent Suyenaga

5

1 reference

25 September 2017

Martin Moorhead

6

1 reference

25 September 2017

Jim Eberle

7

1 reference

25 September 2017

Yvonne R Thorstenson

8

1 reference

25 September 2017

Ted Jones

9

1 reference

25 September 2017

Ronald W Davis

10

1 reference

25 September 2017

Eugeni Namsaraev

11

1 reference

25 September 2017

Malek Faham

12

1 reference

25 September 2017

1 July 2004

1 reference

25 September 2017

1 reference

25 September 2017

14

1 reference

25 September 2017

7

1 reference

25 September 2017

1404-1412

1 reference

The International HapMap Project

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Human genome sequence variation and the influence of gene history, mutation and recombination

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

The structure of haplotype blocks in the human genome

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

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

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Characterization of single-nucleotide polymorphisms in coding regions of human genes

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Mechanisms and biological effects of mismatch repair

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

26 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Mismatch repair detection (MRD): high-throughput scanning for DNA variations

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

DNA pooling in mutation detection with reference to sequence analysis

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

A first-generation linkage disequilibrium map of human chromosome 22

19 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Comparative Analysis of Human DNA Variations by Fluorescence-Based Sequencing of PCR Products

2 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=442157

Variation is the spice of life

2 December 2018

1 reference

12 December 2020

Haplotype tagging for the identification of common disease genes

1 reference

12 December 2020

Detection of rare K-ras codon 12 mutations using allele-specific competitive blocker PCR

1 reference

12 December 2020

Rapid and simultaneous detection of multiple mutations by pooled and multiplex single nucleotide primer extension: application to the study of insulin-responsive glucose transporter and insulin receptor mutations in non-insulindependent diabetes

1 reference

12 December 2020

Detection of basepair substitution mutation at a frequency of 1 x 10(-7) by combining two genotypic selection methods, MutEx enrichment and allele-specific competitive blocker PCR

1 reference

12 December 2020

High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC)

1 reference

12 December 2020

Identifiers

DOI

10.1101/GR.2373904

1 reference

25 September 2017

1 reference

25 September 2017

PubMed publication ID

15231755

1 reference