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Quality and completeness of SNP databases
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
title
Quality and completeness of SNP databases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
main subject
database
0 references
author
David Altshuler
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
Stacey Gabriel
series ordinal
2
object named as
Stacey B Gabriel
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
David Reich
series ordinal
1
object named as
David E Reich
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
language of work or name
English
0 references
publication date
24 March 2003
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
published in
Nature Genetics
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stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
volume
33
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
page(s)
457-458
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
exact match
https://scigraph.springernature.com/pub.10.1038/ng1133
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cites work
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
1 reference
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reference URL
https://api.crossref.org/works/10.1038%2FNG1133
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7 January 2021
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The Sequence of the Human Genome
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reference URL
https://api.crossref.org/works/10.1038%2FNG1133
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7 January 2021
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inferred from DOI database lookup
Single-nucleotide polymorphisms in the public domain: how useful are they?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage disequilibrium in the human genome
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The structure of haplotype blocks in the human genome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variation is the spice of life
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reference URL
https://api.crossref.org/works/10.1038%2FNG1133
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7 January 2021
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inferred from DOI database lookup
Genetic structure of human populations
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chip-based genotyping by mass spectrometry
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Initial sequencing and analysis of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1133
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1133
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
PubMed ID
12652301
1 reference
stated in
Europe PubMed Central
PubMed ID
12652301
retrieved
31 July 2017
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