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Web-Based Database and Viewer of East Asian Copy Number Variations
We have discovered copy number variations (CNVs) in 3,578 Korean individuals with the Affymetrix Genome-Wide SNP array 5.0, and 4,003 copy number variation regions (CNVRs) were defined in a previous study. To explore the details of the variants easily in related studies, we built a database, catalog...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korea Genome Organization
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475484/ https://www.ncbi.nlm.nih.gov/pubmed/23105931 http://dx.doi.org/10.5808/GI.2012.10.1.65 |
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author | Kim, Ji-Hong Hu, Hae-Jin Chung, Yeun-Jun |
author_facet | Kim, Ji-Hong Hu, Hae-Jin Chung, Yeun-Jun |
author_sort | Kim, Ji-Hong |
collection | PubMed |
description | We have discovered copy number variations (CNVs) in 3,578 Korean individuals with the Affymetrix Genome-Wide SNP array 5.0, and 4,003 copy number variation regions (CNVRs) were defined in a previous study. To explore the details of the variants easily in related studies, we built a database, cataloging the CNVs and related information. This system helps researchers browsing these variants with gene and structure variant annotations. Users can easily find specific regions with search options and verify them from system-integrated genome browsers with annotations. |
format | Online Article Text |
id | pubmed-3475484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korea Genome Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-34754842012-10-26 Web-Based Database and Viewer of East Asian Copy Number Variations Kim, Ji-Hong Hu, Hae-Jin Chung, Yeun-Jun Genomics Inf Application Note We have discovered copy number variations (CNVs) in 3,578 Korean individuals with the Affymetrix Genome-Wide SNP array 5.0, and 4,003 copy number variation regions (CNVRs) were defined in a previous study. To explore the details of the variants easily in related studies, we built a database, cataloging the CNVs and related information. This system helps researchers browsing these variants with gene and structure variant annotations. Users can easily find specific regions with search options and verify them from system-integrated genome browsers with annotations. Korea Genome Organization 2012-03 2012-03-31 /pmc/articles/PMC3475484/ /pubmed/23105931 http://dx.doi.org/10.5808/GI.2012.10.1.65 Text en Copyright © 2012 by The Korea Genome Organization http://creativecommons.org/licenses/by-nc/3.0 It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/). |
spellingShingle | Application Note Kim, Ji-Hong Hu, Hae-Jin Chung, Yeun-Jun Web-Based Database and Viewer of East Asian Copy Number Variations |
title | Web-Based Database and Viewer of East Asian Copy Number Variations |
title_full | Web-Based Database and Viewer of East Asian Copy Number Variations |
title_fullStr | Web-Based Database and Viewer of East Asian Copy Number Variations |
title_full_unstemmed | Web-Based Database and Viewer of East Asian Copy Number Variations |
title_short | Web-Based Database and Viewer of East Asian Copy Number Variations |
title_sort | web-based database and viewer of east asian copy number variations |
topic | Application Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3475484/ https://www.ncbi.nlm.nih.gov/pubmed/23105931 http://dx.doi.org/10.5808/GI.2012.10.1.65 |
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