Genome-wide evaluation of the public SNP databases. (Q52956509)

9 May 2018

title

Genome-wide evaluation of the public SNP databases. (English)

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9 May 2018

author

Richard S. Judson

5

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9 May 2018

author name string

Ruhong Jiang

1

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9 May 2018

Jicheng Duan

2

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9 May 2018

Andreas Windemuth

3

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9 May 2018

J Claiborne Stephens

4

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9 May 2018

Chuanbo Xu

6

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9 May 2018

publication date

1 November 2003

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9 May 2018

published in

Pharmacogenomics

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9 May 2018

volume

4

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9 May 2018

page(s)

779-789

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9 May 2018

issue

6

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9 May 2018

Initial sequencing and analysis of the human genome

cites work

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https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

dbSNP: the NCBI database of genetic variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Haplotype variation and linkage disequilibrium in 313 human genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Normal telomere lengths found in cloned cattle

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Quality and completeness of SNP databases

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Base-calling of automated sequencer traces using phred. I. Accuracy assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

An SNP map of human chromosome 22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Data mining of public SNP databases for the selection of intragenic SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Amino acid difference formula to help explain protein evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Recombinational and mutational hotspots within the human lipoprotein lipase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Neighboring-nucleotide effects on single nucleotide polymorphisms: a study of 2.6 million polymorphisms across the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Interrogating a high-density SNP map for signatures of natural selection

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Genomics. New mapping project splits the community.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Human genome. Reaching their goal early, sequencing labs celebrate

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

DNA variability of human genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

… as consortium plans free SNP map of human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2FPHGS.4.6.779.22821

10.1517/PHGS.4.6.779.22821

21 January 2018

Identifiers

DOI

1 reference

9 May 2018

release_anwe2yp5sbhrlb472d5j46xyaa

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/anwe2yp5sbhrlb472d5j46xyaa

mapped directly with Wikidata item

24 November 2022

based on heuristic

PubMed ID

14596641

1 reference

9 May 2018