Centromere reference models for human chromosomes X and Y satellite arrays

The human genome sequence remains incomplete, with multimegabase-sized gaps representing the endogenous centromeres and other heterochromatic regions. Available sequence-based studies within these sites in the genome have demonstrated a role in centromere function and chromosome pairing, necessary t...

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Detalles Bibliográficos
Autores principales: Miga, Karen H., Newton, Yulia, Jain, Miten, Altemose, Nicolas, Willard, Huntington F., Kent, W. James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2014
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975068/
https://www.ncbi.nlm.nih.gov/pubmed/24501022
http://dx.doi.org/10.1101/gr.159624.113

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975068/
https://www.ncbi.nlm.nih.gov/pubmed/24501022
http://dx.doi.org/10.1101/gr.159624.113

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