Cargando…
Insertion-deletions burden in copy number polymorphisms of the Tibetan population
BACKGROUND: Many studies have been conducted to identify either insertions-deletions (inDels) or copy number variations (CNVs) in humans, but few studies have been conducted to identify both of these forms coexisting in the same region. AIMS AND OBJECTIVES: To map the functionally significant sites...
Autores principales: | Veerappa, Avinash M., Vishweswaraiah, Sangeetha, Lingaiah, Kusuma, Murthy, N. Megha, Suresh, Raviraj V., Belur, Keshava, Ramachandra, Nallur B., Tejaswini, Patel, Niveditha B., Gowda, P. K. Supriya |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228569/ https://www.ncbi.nlm.nih.gov/pubmed/25400346 http://dx.doi.org/10.4103/0971-6866.142888 |
Ejemplares similares
-
Global Spectrum of Copy Number Variations Reveals Genome Organizational Plasticity and Proposes New Migration Routes
por: Veerappa, Avinash M., et al.
Publicado: (2015) -
Unravelling the Complexity of Human Olfactory Receptor Repertoire by Copy Number Analysis across Population Using High Resolution Arrays
por: Veerappa, Avinash M., et al.
Publicado: (2013) -
Copy Number Variations Burden on miRNA Genes Reveals Layers of Complexities Involved in the Regulation of Pathways and Phenotypic Expression
por: Veerappa, Avinash M., et al.
Publicado: (2014) -
Identifying the risk of producing aneuploids using meiotic recombination genes as biomarkers: A copy number variation approach
por: Suresh, Raviraj V., et al.
Publicado: (2017) -
Copy Number Variation Burden on Asthma Subgenome in Normal Cohorts Identifies Susceptibility Markers
por: Vishweswaraiah, Sangeetha, et al.
Publicado: (2015)