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Read-depth based approach on whole genome resequencing data reveals important insights into the copy number variation (CNV) map of major global buffalo breeds

BACKGROUND: Elucidating genome-wide structural variants including copy number variations (CNVs) have gained increased significance in recent times owing to their contribution to genetic diversity and association with important pathophysiological states. The present study aimed to elucidate the high-...

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Detalles Bibliográficos
Autores principales: Ahmad, Sheikh Firdous, Chandrababu Shailaja, Celus, Vaishnav, Sakshi, Kumar, Amit, Gaur, Gyanendra Kumar, Janga, Sarath Chandra, Ahmad, Syed Mudasir, Malla, Waseem Akram, Dutt, Triveni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10580622/
https://www.ncbi.nlm.nih.gov/pubmed/37845620
http://dx.doi.org/10.1186/s12864-023-09720-8