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HvrBase++: a phylogenetic database for primate species

HvrBase++ is the improved and extended version of HvrBase. Extensions are made by adding more population-based sequence samples from all primates including humans. The current collection comprises 13 873 hypervariable region I (HVRI) sequences and 4940 hypervariable region II (HVRII) sequences. In a...

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Detalles Bibliográficos
Autores principales: Kohl, Jochen, Paulsen, Ingo, Laubach, Thomas, Radtke, Achim, von Haeseler, Arndt
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347393/
https://www.ncbi.nlm.nih.gov/pubmed/16381963
http://dx.doi.org/10.1093/nar/gkj030
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author Kohl, Jochen
Paulsen, Ingo
Laubach, Thomas
Radtke, Achim
von Haeseler, Arndt
author_facet Kohl, Jochen
Paulsen, Ingo
Laubach, Thomas
Radtke, Achim
von Haeseler, Arndt
author_sort Kohl, Jochen
collection PubMed
description HvrBase++ is the improved and extended version of HvrBase. Extensions are made by adding more population-based sequence samples from all primates including humans. The current collection comprises 13 873 hypervariable region I (HVRI) sequences and 4940 hypervariable region II (HVRII) sequences. In addition, we included 1376 complete mitochondrial genomes, 205 sequences from X-chromosomal loci and 202 sequences from autosomal chromosomes 1, 8, 11 and 16. In order to reduce the introduction of erroneous data into HvrBase++, we have developed a procedure that monitors GenBank for new versions of the current data in HvrBase++ and automatically updates the collection if necessary. For the stored sequences, supplementary information such as geographic origin, population affiliation and language of the sequence donor can be retrieved. HvrBase++ is Oracle based and easily accessible by a web interface (). As a new key feature, HvrBase++ provides an interactive graphical tool to easily access data from dynamically created geographical maps.
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spelling pubmed-13473932006-01-25 HvrBase++: a phylogenetic database for primate species Kohl, Jochen Paulsen, Ingo Laubach, Thomas Radtke, Achim von Haeseler, Arndt Nucleic Acids Res Article HvrBase++ is the improved and extended version of HvrBase. Extensions are made by adding more population-based sequence samples from all primates including humans. The current collection comprises 13 873 hypervariable region I (HVRI) sequences and 4940 hypervariable region II (HVRII) sequences. In addition, we included 1376 complete mitochondrial genomes, 205 sequences from X-chromosomal loci and 202 sequences from autosomal chromosomes 1, 8, 11 and 16. In order to reduce the introduction of erroneous data into HvrBase++, we have developed a procedure that monitors GenBank for new versions of the current data in HvrBase++ and automatically updates the collection if necessary. For the stored sequences, supplementary information such as geographic origin, population affiliation and language of the sequence donor can be retrieved. HvrBase++ is Oracle based and easily accessible by a web interface (). As a new key feature, HvrBase++ provides an interactive graphical tool to easily access data from dynamically created geographical maps. Oxford University Press 2006-01-01 2005-12-28 /pmc/articles/PMC1347393/ /pubmed/16381963 http://dx.doi.org/10.1093/nar/gkj030 Text en © The Author 2006. Published by Oxford University Press. All rights reserved
spellingShingle Article
Kohl, Jochen
Paulsen, Ingo
Laubach, Thomas
Radtke, Achim
von Haeseler, Arndt
HvrBase++: a phylogenetic database for primate species
title HvrBase++: a phylogenetic database for primate species
title_full HvrBase++: a phylogenetic database for primate species
title_fullStr HvrBase++: a phylogenetic database for primate species
title_full_unstemmed HvrBase++: a phylogenetic database for primate species
title_short HvrBase++: a phylogenetic database for primate species
title_sort hvrbase++: a phylogenetic database for primate species
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347393/
https://www.ncbi.nlm.nih.gov/pubmed/16381963
http://dx.doi.org/10.1093/nar/gkj030
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