(Q36099362)

12 August 2017

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title

Applications of whole-genome high-density SNP genotyping (English)

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12 August 2017

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whole genome sequencing

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David W Craig

1

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12 August 2017

Dietrich A Stephan

series ordinal

2

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12 August 2017

publication date

1 March 2005

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Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

12 August 2017

published in

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12 August 2017

volume

5

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12 August 2017

issue

2

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12 August 2017

page(s)

159-170

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Patterns of linkage disequilibrium in the human genome

12 August 2017

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

21 January 2018

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Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function

21 January 2018

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Highly parallel SNP genotyping

21 January 2018

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Decoding randomly ordered DNA arrays

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A highly informative SNP linkage panel for human genetic studies.

21 January 2018

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Association testing by DNA pooling: an effective initial screen

21 January 2018

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Mining disease susceptibility genes through SNP analyses and expression profiling using MALDI-TOF mass spectrometry

21 January 2018

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21 January 2018

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A 3.9-centimorgan-resolution human single-nucleotide polymorphism linkage map and screening set.

21 January 2018

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A HOX gene mutation in a family with isolated congenital vertical talus and Charcot-Marie-Tooth disease

21 January 2018

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Comparison of microsatellites versus single-nucleotide polymorphisms in a genome linkage screen for prostate cancer-susceptibility Loci

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Genomewide linkage searches for Mendelian disease loci can be efficiently conducted using high-density SNP genotyping arrays

21 January 2018

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Construction of multilocus genetic linkage maps in humans

21 January 2018

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dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

21 January 2018

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Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays

21 January 2018

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Genome-wide detection of LOH in prostate cancer using human SNP microarray technology

21 January 2018

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Single nucleotide polymorphism array analysis of flow-sorted epithelial cells from frozen versus fixed tissues for whole genome analysis of allelic loss in breast cancer

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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How many diseases does it take to map a gene with SNPs?

21 January 2018

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Searching for genetic determinants in the new millennium

21 January 2018

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Linkage disequilibrium in the human genome

21 January 2018

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Haplotype blocks and linkage disequilibrium in the human genome

21 January 2018

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Association study designs for complex diseases

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Detect and adjust for population stratification in population-based association study using genomic control markers: an application of Affymetrix Genechip Human Mapping 10K array.

21 January 2018

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A polygenic basis for late-onset disease

21 January 2018

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Genetic association mapping at the crossroads: which test and why? Overview and practical guidelines

21 January 2018

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

21 January 2018

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Amino acid variant in the kinase binding domain of dual-specific A kinase-anchoring protein 2: a disease susceptibility polymorphism

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

Genotyping pooled DNA on microarrays: a systematic genome screen of thousands of SNPs in large samples to detect QTLs for complex traits.

21 January 2018

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dbSNP: the NCBI database of genetic variation

21 January 2018

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The Sequence of the Human Genome

21 January 2018

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Bayesian approach to discovering pathogenic SNPs in conserved protein domains

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

A full-likelihood method for the evaluation of causality of sequence variants from family data

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

Amino acid difference formula to help explain protein evolution

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

Human Gene Mutation Database (HGMD): 2003 update

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

New developments in high-throughput resequencing and variation detection using high density microarrays

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

A General Model for the Genetic Analysis of Pedigree Data

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

21 January 2018

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https://api.crossref.org/works/10.1586%2F14737159.5.2.159

21 January 2018

Identifiers

DOI

10.1586/14737159.5.2.159

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12 August 2017

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