SNPing in the human genome (Q34134790)

31 July 2017

title

SNPing in the human genome (English)

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31 July 2017

Carlson CS

1

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31 July 2017

Newman TL

series ordinal

2

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31 July 2017

Nickerson DA

series ordinal

3

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31 July 2017

publication date

1 February 2001

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Current Opinion in Chemical Biology

31 July 2017

language of work or name

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1 reference

31 July 2017

volume

5

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31 July 2017

issue

1

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31 July 2017

page(s)

78-85

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publication type of scholarly work

31 July 2017

review article

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Positional cloning moves from perditional to traditional

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Searching for genetic determinants in the new millennium

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

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Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28

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The genetically isolated populations of Finland and Sardinia may not be a panacea for linkage disequilibrium mapping of common disease genes

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Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus

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Localization of a small genomic region associated with elevated ACE

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Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs

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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

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Sequence diversity in 36 candidate genes for cardiovascular disorders

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

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Overlapping Genomic Sequences: A Treasure Trove of Single-Nucleotide Polymorphisms

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A general approach to single-nucleotide polymorphism discovery

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Identification of candidate coding region single nucleotide polymorphisms in 165 human genes using assembled expressed sequence tags

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Reliable identification of large numbers of candidate SNPs from public EST data

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Base-Calling of Automated Sequencer Traces UsingPhred. I. Accuracy Assessment

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Single nucleotide polymorphism hunting in cyberspace

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Genome-wide analysis of single-nucleotide polymorphisms in human expressed sequences

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Single-nucleotide polymorphisms can cause different structural folds of mRNA.

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

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

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

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PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

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Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

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Accessing genetic information with high-density DNA arrays

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Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis

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Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography

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Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

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Screening for mutations by enzyme mismatch cleavage with T4 endonuclease VII.

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Detection of mutations in human genes by a new rapid method: cleavage fragment length polymorphism analysis (CFLPA)

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Position and degree of mismatches and the mobility of DNA heteroduplexes

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Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

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

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Multiplex detection of single-nucleotide variations using molecular beacons

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Genetic Bit Analysis: a solid phase method for typing single nucleotide polymorphisms

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From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms

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

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A novel method for detecting point mutations or polymorphisms and its application to population screening for carriers of phenylketonuria

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Multiplexed single nucleotide polymorphism genotyping by oligonucleotide ligation and flow cytometry

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Homogeneous genotyping assays for single nucleotide polymorphisms with fluorescence resonance energy transfer detection

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Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes

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Allelic discrimination using fluorogenic probes and the 5' nuclease assay

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Fluorescence-based DNA minisequence analysis for detection of known single-base changes in genomic DNA

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High-density multiplex detection of nucleic acid sequences: oligonucleotide ligation assay and sequence-coded separation

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

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A Homogeneous, Ligase-Mediated DNA Diagnostic Test

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

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

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

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

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Association mapping of disease loci, by use of a pooled DNA genomic screen

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The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases I. DNA pooling

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Quantitative approach to single-nucleotide polymorphism analysis using MALDI-TOF mass spectrometry

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

1 reference

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

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Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness

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Identifiers

DOI

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31 July 2017

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