Publication
Chromosome structural variants: Epidemiology, identification and contribution to human diseases
| dc.contributor.author | Dong, Zirui | |
| dc.contributor.author | David, Dezso | |
| dc.contributor.author | Gonzaga-Jauregui, Claudia | |
| dc.contributor.author | Morton, Cynthia C. | |
| dc.contributor.author | Zepeda-Mendoza, Cinthya J. | |
| dc.date.accessioned | 2023-02-28T14:53:00Z | |
| dc.date.available | 2023-02-28T14:53:00Z | |
| dc.date.issued | 2022-09-09 | |
| dc.description | Editorial on the Research Topic: Chromosome structural variants: Epidemiology, identification and contribution to human diseases. | pt_PT |
| dc.description.abstract | Human chromosome structural variants (SVs) are balanced/unbalanced genomic abnormalities that include translocation, inversion, insertion, and deletion/duplication (also known as copy-number variants, CNVs) events with a size of >50 bp. Currently, the capability of genome sequencing in the research and clinical fields has increased our capacity to detect cryptic SVs and further delineate the complexity of karyotypically/microarray detectable SVs. This has increased our knowledge of pathogenicity mechanisms by considering dysregulation of gene expression through position effects and complex interactions between gene dosage and mutational burden. However, much of the contribution of SVs to human disease is left to explore, as the incidence of SVs is still underestimated owing to limitations of current sequencing technologies and analytical pipelines, and few studies have comprehensively integrated SV information with single nucleotide variants in congenital diseases. Rigorous investigation of SV pathogenicity is warranted for clinical applications. The Research Topic in this issue is divided into three main sections: three articles demonstrate methodologies in SV identification and pathogenicity annotation; five papers discuss the spectrum of SVs in individuals with different indications; and two reports characterize sequence complexity of SVs [...]. | pt_PT |
| dc.description.sponsorship | CCM acknowledges NIH P01 GM061354 and support by the NIHR Manchester Biomedical Research Centre | pt_PT |
| dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
| dc.identifier.citation | Front Genet. 2022 Sep 9;13:1022918. doi: 10.3389/fgene.2022.1022918. eCollection 2022. Editorial | pt_PT |
| dc.identifier.doi | 10.3389/fgene.2022.1022918 | pt_PT |
| dc.identifier.issn | 1664-8021 | |
| dc.identifier.uri | http://hdl.handle.net/10400.18/8540 | |
| dc.language.iso | eng | pt_PT |
| dc.peerreviewed | yes | pt_PT |
| dc.publisher | Frontiers Media | pt_PT |
| dc.relation.publisherversion | https://www.frontiersin.org/articles/10.3389/fgene.2022.1022918/full | pt_PT |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | pt_PT |
| dc.subject | SV Mechanisms | pt_PT |
| dc.subject | SV Spectrum | pt_PT |
| dc.subject | Annotation and Prediction | pt_PT |
| dc.subject | Genomic Rearrangements | pt_PT |
| dc.subject | Genomic Variation | pt_PT |
| dc.subject | Methodologies & Tools | pt_PT |
| dc.subject | Sequence Complexity | pt_PT |
| dc.subject | Structural Variant | pt_PT |
| dc.subject | Doenças Genéticas | pt_PT |
| dc.subject | Doenças Genómicas | pt_PT |
| dc.title | Chromosome structural variants: Epidemiology, identification and contribution to human diseases | pt_PT |
| dc.type | journal article | |
| dspace.entity.type | Publication | |
| oaire.citation.startPage | 1022918 | pt_PT |
| oaire.citation.title | Frontiers in Genetics | pt_PT |
| oaire.citation.volume | 13 | pt_PT |
| rcaap.embargofct | Acesso de acordo com política editorial da revista. | pt_PT |
| rcaap.rights | openAccess | pt_PT |
| rcaap.type | article | pt_PT |