Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1034001
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dc.contributor.authorSILVA, J. M. dapt_BR
dc.contributor.authorROMANIUC, A. R.pt_BR
dc.contributor.authorCAETANO, A. R.pt_BR
dc.contributor.authorGIACHETTO, P. F.pt_BR
dc.contributor.authorYAMAGISHI, M. E. B.pt_BR
dc.date.accessioned2016-01-15T11:11:11Zpt_BR
dc.date.available2016-01-15T11:11:11Zpt_BR
dc.date.created2016-01-15pt_BR
dc.date.issued2015pt_BR
dc.identifier.citationIn: PLANT & ANIMAL GENOME CONFERENCE, 23., 2015, San Diego, CA. [Abstracts...]. San Diego: [s.n.], 2015.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1034001pt_BR
dc.descriptionCNVs (Copy Number Variations) are defined as copy number variations of DNA fragments typically larger than one kilobase (Kb), but less than five megabases (Mb). They represent a genomic disequilibrium that alters the ploidy in a specific locus within an individual, which may also be observed with varying frequencies within a population. An initial study estimated that 12% of the human genome shows this type of structural variation. Reliable tools have been developed to detect CNVs from molecular data produced with three main platforms: Comparative Genomic Hybridization (CGH) arrays, Single Nucleotide Polymorphism (SNP) genotyping arrays, and DNA Next-Generation Sequencing (NGS). However, processes for merging overlapping CNVs into a meaningful set of discrete Copy Number Variable Regions (CNVRs) need improvement, particularly when several CNV patterns co-exist within the same genomic locus. Available algorithms frequently merge noncontiguous CNVRs or fragment large CNVRs into multiple regions. A new web-based software (Java Merging Copy Number Variants: JM-CNV) was developed to address the aforementioned issues.pt_BR
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectCopy Number Variationspt_BR
dc.subjectBioinformáticapt_BR
dc.titleJava Merging Copy Number Variants (JM-CNV): a new algorithm for identifying Copy Number Variant Regions (CNVR).pt_BR
dc.typeResumo em anais e proceedingspt_BR
dc.date.updated2020-01-21T11:11:11Zpt_BR
dc.subject.nalthesaurusComputer softwarept_BR
dc.subject.nalthesaurusBioinformaticspt_BR
dc.description.notesPAG 2015. Pôster P1170.pt_BR
dc.format.extent2Não paginado.pt_BR
riaa.ainfo.id1034001pt_BR
riaa.ainfo.lastupdate2020-01-21 -02:00:00pt_BR
dc.contributor.institutionJOAQUIM MANOEL DA SILVA, Unemat; ALAN ROBERTO ROMANIUC, CNPTIA; ALEXANDRE RODRIGUES CAETANO, CENARGEN; POLIANA FERNANDA GIACHETTO, CNPTIA; MICHEL EDUARDO BELEZA YAMAGISHI, CNPTIA.pt_BR
Aparece nas coleções:Resumo em anais de congresso (CNPTIA)

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