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Variation resources at UC Santa Cruz

The variation resources within the University of California Santa Cruz Genome Browser include polymorphism data drawn from public collections and analyses of these data, along with their display in the context of other genomic annotations. Primary data from dbSNP is included for many organisms, with...

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Detalles Bibliográficos
Autores principales: Thomas, Daryl J., Trumbower, Heather, Kern, Andrew D., Rhead, Brooke L., Kuhn, Robert M., Haussler, David, Kent, W. James
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781230/
https://www.ncbi.nlm.nih.gov/pubmed/17151077
http://dx.doi.org/10.1093/nar/gkl953
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author Thomas, Daryl J.
Trumbower, Heather
Kern, Andrew D.
Rhead, Brooke L.
Kuhn, Robert M.
Haussler, David
Kent, W. James
author_facet Thomas, Daryl J.
Trumbower, Heather
Kern, Andrew D.
Rhead, Brooke L.
Kuhn, Robert M.
Haussler, David
Kent, W. James
author_sort Thomas, Daryl J.
collection PubMed
description The variation resources within the University of California Santa Cruz Genome Browser include polymorphism data drawn from public collections and analyses of these data, along with their display in the context of other genomic annotations. Primary data from dbSNP is included for many organisms, with added information including genomic alleles and orthologous alleles for closely related organisms. Display filtering and coloring is available by variant type, functional class or other annotations. Annotation of potential errors is highlighted and a genomic alignment of the variant's flanking sequence is displayed. HapMap allele frequencies and linkage disequilibrium (LD) are available for each HapMap population, along with non-human primate alleles. The browsing and analysis tools, downloadable data files and links to documentation and other information can be found at .
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spelling pubmed-17812302007-02-22 Variation resources at UC Santa Cruz Thomas, Daryl J. Trumbower, Heather Kern, Andrew D. Rhead, Brooke L. Kuhn, Robert M. Haussler, David Kent, W. James Nucleic Acids Res Articles The variation resources within the University of California Santa Cruz Genome Browser include polymorphism data drawn from public collections and analyses of these data, along with their display in the context of other genomic annotations. Primary data from dbSNP is included for many organisms, with added information including genomic alleles and orthologous alleles for closely related organisms. Display filtering and coloring is available by variant type, functional class or other annotations. Annotation of potential errors is highlighted and a genomic alignment of the variant's flanking sequence is displayed. HapMap allele frequencies and linkage disequilibrium (LD) are available for each HapMap population, along with non-human primate alleles. The browsing and analysis tools, downloadable data files and links to documentation and other information can be found at . Oxford University Press 2007-01 2006-12-06 /pmc/articles/PMC1781230/ /pubmed/17151077 http://dx.doi.org/10.1093/nar/gkl953 Text en © 2006 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Thomas, Daryl J.
Trumbower, Heather
Kern, Andrew D.
Rhead, Brooke L.
Kuhn, Robert M.
Haussler, David
Kent, W. James
Variation resources at UC Santa Cruz
title Variation resources at UC Santa Cruz
title_full Variation resources at UC Santa Cruz
title_fullStr Variation resources at UC Santa Cruz
title_full_unstemmed Variation resources at UC Santa Cruz
title_short Variation resources at UC Santa Cruz
title_sort variation resources at uc santa cruz
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781230/
https://www.ncbi.nlm.nih.gov/pubmed/17151077
http://dx.doi.org/10.1093/nar/gkl953
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