Загрузка...
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...
Сохранить в:
| Опубликовано в: : | Mob DNA |
|---|---|
| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
BioMed Central
2016
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4967303/ https://ncbi.nlm.nih.gov/pubmed/27478512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13100-016-0072-x |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|