Toward genome-wide SNP genotyping (Q40419131)

20 September 2017

title

Toward genome-wide SNP genotyping (English)

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20 September 2017

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Ann-Christine Syvänen

series ordinal

1

object named as

Ann-Christine Syvänen

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publication date

1 June 2005

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20 September 2017

language of work or name

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20 September 2017

volume

37 Suppl

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20 September 2017

page(s)

S5-10

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Genome-wide association studies for common diseases and complex traits

20 September 2017

cites work

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The International HapMap Project

21 January 2018

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Whole-genome patterns of common DNA variation in three human populations

21 January 2018

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Genotype prediction using a dense map of SNPs

21 January 2018

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Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations

21 January 2018

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21 January 2018

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[21] Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction

21 January 2018

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Multiplex genotype determination at a large number of gene loci

21 January 2018

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The elimination of primer-dimer accumulation in PCR

21 January 2018

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Large-scale genotyping of complex DNA.

21 January 2018

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An SNP map of the human genome generated by reduced representation shotgun sequencing

21 January 2018

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Flexible use of high-density oligonucleotide arrays for single-nucleotide polymorphism discovery and validation

21 January 2018

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Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

21 January 2018

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

21 January 2018

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Multiplexed genotyping with sequence-tagged molecular inversion probes

21 January 2018

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Highly multiplexed molecular inversion probe genotyping: over 10,000 targeted SNPs genotyped in a single tube assay

21 January 2018

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A genome-wide scalable SNP genotyping assay using microarray technology

21 January 2018

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Accessing genetic variation: genotyping single nucleotide polymorphisms

21 January 2018

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Methods for Genotyping Single Nucleotide Polymorphisms

21 January 2018

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Algorithms for large-scale genotyping microarrays

21 January 2018

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A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

21 January 2018

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Universal DNA microarray method for multiplex detection of low abundance point mutations

21 January 2018

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Quantitative phenotypic analysis of yeast deletion mutants using a highly parallel molecular bar-coding strategy

21 January 2018

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Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays

21 January 2018

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SBE-TAGS: an array-based method for efficient single-nucleotide polymorphism genotyping

21 January 2018

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Multiplex SNP genotyping in pooled DNA samples by a four-colour microarray system

21 January 2018

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A microsphere-based assay for multiplexed single nucleotide polymorphism analysis using single base chain extension

21 January 2018

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Parallel gene analysis with allele-specific padlock probes and tag microarrays

21 January 2018

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Decoding randomly ordered DNA arrays

21 January 2018

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Guidelines for genotyping in genomewide linkage studies: single-nucleotide-polymorphism maps versus microsatellite maps

21 January 2018

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Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

21 January 2018

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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

21 January 2018

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Template-directed dye-terminator incorporation (TDI) assay: a homogeneous DNA diagnostic method based on fluorescence resonance energy transfer

21 January 2018

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Application of pooled genotyping to scan candidate regions for association with HDL cholesterol levels

21 January 2018

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The impact of SNP density on fine-scale patterns of linkage disequilibrium

21 January 2018

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Arrayed primer extension: solid-phase four-color DNA resequencing and mutation detection technology

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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Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellites

21 January 2018

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An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.

21 January 2018

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Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus

21 January 2018

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A high-throughput SNP typing system for genome-wide association studies

21 January 2018

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The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

21 January 2018

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Variation is the spice of life

21 January 2018

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7 January 2021

The future of genetic studies of complex human diseases

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7 January 2021

Haplotype tagging for the identification of common disease genes

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7 January 2021

From signatures to models: understanding cancer using microarrays

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7 January 2021

Array comparative genomic hybridization and its applications in cancer

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7 January 2021

Genetic analysis of amplified DNA with immobilized sequence-specific oligonucleotide probes

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7 January 2021

AFLP: a new technique for DNA fingerprinting

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7 January 2021

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

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7 January 2021

Light-directed, spatially addressable parallel chemical synthesis

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7 January 2021

Padlock Probes: Circularizing Oligonucleotides for Localized DNA Detection

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7 January 2021

Highly parallel SNP genotyping

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7 January 2021

A Ligase-Mediated Gene Detection Technique

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7 January 2021

Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

1 reference

7 January 2021

A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E

1 reference

7 January 2021

Analyzing and comparing nucleic acid sequences by hybridization to arrays of oligonucleotides: evaluation using experimental models

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7 January 2021

Light-generated oligonucleotide arrays for rapid DNA sequence analysis

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7 January 2021

High-Throughput Variation Detection and Genotyping Using Microarrays

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7 January 2021

Mutation detection by solid phase primer extension

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7 January 2021

Minisequencing: a specific tool for DNA analysis and diagnostics on oligonucleotide arrays.

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7 January 2021

Flow cytometry-based minisequencing: a new platform for high-throughput single-nucleotide polymorphism scoring

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7 January 2021

Universal DNA array detection of small insertions and deletions in BRCA1 and BRCA2

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7 January 2021

Genome-wide association studies: theoretical and practical concerns

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7 January 2021

A highly informative SNP linkage panel for human genetic studies.

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7 January 2021

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

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7 January 2021

Identifiers

DOI

10.1038/NG1558

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Dimensions Publication ID

20 September 2017

1046319442

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