Identification of polymorphic SVA retrotransposons using a mobile element scanning method for SVA (ME-Scan-SVA)

BACKGROUND: Mobile element insertions are a major source of human genomic variation. SVA (SINE-R/VNTR/Alu) is the youngest retrotransposon family in the human genome and a number of diseases are known to be caused by SVA insertions. However, inter-individual genomic variations generated by SVA inser...

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Detalles Bibliográficos
Autores principales: Ha, Hongseok, Loh, Jui Wan, Xing, Jinchuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967303/
https://www.ncbi.nlm.nih.gov/pubmed/27478512
http://dx.doi.org/10.1186/s13100-016-0072-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4967303/
https://www.ncbi.nlm.nih.gov/pubmed/27478512
http://dx.doi.org/10.1186/s13100-016-0072-x

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