CNVVdb: a database of copy number variations across vertebrate genomes.

Feng-Chi Chen, Yen-Zho Chen, Trees-Juen Chuang
Author Information
  1. Feng-Chi Chen: Division of Biostatistics and Bioinformatics, Institute of Population Health Sciences, National Health Research Institutes, Miaoli County 350, Taipei, Taiwan.

Abstract

SUMMARY: CNVVdb is a web interface for identification of putative copy number variations (CNVs) among 16 vertebrate species using the-same-species self-alignments and cross-species pairwise alignments. By querying genomic coordinates in the target species, all the potential paralogous/orthologous regions that overlap > or = 80-100% (adjustable) of the query sequences with user-specified sequence identity (> or = 60% ~ > or = 90%) are returned. Additional information is also given for the genes that are included in the returned regions, including gene description, alternatively spliced transcripts, gene ontology descriptions and other biologically important information. CNVVdb also provides information of pseudogenes and single nucleotide polymorphisms (SNPs) for the CNV-related genomic regions. Moreover, multiple sequence alignments of shared CNVs across species are also provided. With the combination of CNV, SNP, pseudogene and functional information, CNVVdb can be very useful for comparative and functional studies in vertebrates.
AVAILABILITY: CNVVdb is freely accessible at (http://CNVVdb.genomics.sinica.edu.tw).

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MeSH Term

Animals
Databases, Genetic
Gene Dosage
Genetic Variation
Genome
Genomics
Humans
Internet
Polymorphism, Single Nucleotide
Software

Links to CNCB-NGDC Resources

Database Commons: DBC003229 (CNVVdb)

Word Cloud

Created with Highcharts 10.0.0CNVVdbinformationspeciesregions>=alsocopynumbervariationsCNVsvertebratealignmentsgenomicsequencereturnedgeneacrossfunctionalSUMMARY:webinterfaceidentificationputativeamong16usingthe-same-speciesself-alignmentscross-speciespairwisequeryingcoordinatestargetpotentialparalogous/orthologousoverlap80-100%adjustablequerysequencesuser-specifiedidentity60%~90%AdditionalgivengenesincludedincludingdescriptionalternativelysplicedtranscriptsontologydescriptionsbiologicallyimportantprovidespseudogenessinglenucleotidepolymorphismsSNPsCNV-relatedMoreovermultiplesharedprovidedcombinationCNVSNPpseudogenecanusefulcomparativestudiesvertebratesAVAILABILITY:freelyaccessiblehttp://CNVVdbgenomicssinicaedutwCNVVdb:databasegenomes

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