Cargando…
A Computational Framework Discovers New Copy Number Variants with Functional Importance
Structural variants which cause changes in copy numbers constitute an important component of genomic variability. They account for 0.7% of genomic differences in two individual genomes, of which copy number variants (CNVs) are the largest component. A recent population-based CNV study revealed the n...
Autores principales: | Banerjee, Samprit, Oldridge, Derek, Poptsova, Maria, Hussain, Wasay M., Chakravarty, Dimple, Demichelis, Francesca |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066184/ https://www.ncbi.nlm.nih.gov/pubmed/21479260 http://dx.doi.org/10.1371/journal.pone.0017539 |
Ejemplares similares
-
Impact of constitutional copy number variants on biological pathway evolution
por: Poptsova, Maria, et al.
Publicado: (2013) -
Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays
por: Oldridge, Derek A., et al.
Publicado: (2010) -
A large interactive visual database of copy number variants discovered in taurine cattle
por: Kommadath, Arun, et al.
Publicado: (2019) -
CODEX: a normalization and copy number variation detection method for whole exome sequencing
por: Jiang, Yuchao, et al.
Publicado: (2015) -
A machine learning framework for genotyping the structural variations with copy number variant
por: Zheng, Tian, et al.
Publicado: (2020)