(Q30940258)

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

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27 June 2017

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

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27 June 2017

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Lander ES

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27 June 2017

David Altshuler

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Altshuler D

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27 June 2017

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Pollara VJ

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27 June 2017

Cowles CR

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27 June 2017

Van Etten WJ

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27 June 2017

Baldwin J

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27 June 2017

Linton L

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27 June 2017

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1 September 2000

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27 June 2017

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27 June 2017

407

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27 June 2017

6803

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27 June 2017

513-516

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27 June 2017

The new genomics: global views of biology

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Variations on a theme: cataloging human DNA sequence variation

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The future of genetic studies of complex human diseases

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Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

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

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Genetic epidemiology of single-nucleotide polymorphisms.

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https://api.crossref.org/works/10.1038%2F35035083

7 January 2021

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Human whole-genome shotgun sequencing

1 reference

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Base-calling of automated sequencer traces using phred. II. Error probabilities

1 reference

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

1 reference

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Single nucleotide polymorphism hunting in cyberspace

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A general approach to single-nucleotide polymorphism discovery.

1 reference

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

1 reference

https://api.crossref.org/works/10.1038%2F35035083

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

1 reference

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

1 reference

https://api.crossref.org/works/10.1038%2F35035083

7 January 2021

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

1 reference

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An SNP map of human chromosome 22.

1 reference

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A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

1 reference

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Reading bits of genetic information: methods for single-nucleotide polymorphism analysis

1 reference

https://api.crossref.org/works/10.1038%2F35035083

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Basic local alignment search tool

1 reference

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Sequence diversity in 36 candidate genes for cardiovascular disorders

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7 January 2021

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10.1038/35035083

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Europe PubMed Central

PubMed publication ID

27 June 2017

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PubMed publication ID

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Europe PubMed Central

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27 June 2017

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