Figlerowicz, MarekNature Publishing GroupRepBudzko, L., Marcinkowska-Swojak, M., Jackowiak, P., Kozlowski, P., Figlerowicz, M., 2016. Copy number variation of genes involved in the hepatitis C virus-human inter- actome. Sci. Rep. 6, 31340....
Copy number variations (CNVs) refer to frequently observed structural variations in the form of deletions or duplications greater than 50 base pairs16, which cover more of the genome (total bases) and have a higher mutation rate than single nucleotide polymorphisms (SNPs)17. Similar to SNPs, CNV...
Diet and the evolution of human amylase gene copy number variation. Nat Genet. 2007;39:1256–60. 6. Hollox EJ, Hoh B-P. Human gene copy number variation and infectious disease. Hum Genet. 2014;133:1217–33. 7. Lee C, Scherer SW. The clinical context of copy number variation in the...
Integration of copy number variation and gene expression profiling To identify the significant driver genes that exhibited CNV and gene expression alterations, we integrated the data of significant CNVs and DEGs. Hierarchical clustering analysis of the CNV-driven DEGs was performed using the pheatmap pac...
Copy number variation and antigenic repertoire 来自 国家科技图书文献中心 喜欢 0 阅读量: 34 作者:Armour,AL John 摘要: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human traits and on other model organisms, including ...
Copy number variations (CNVs), which are important source for genetic and phenotypic variation, have been shown to be associated with disease as well as important QTLs, especially in domesticated animals. However, little is known about the CNVs in silkwo
Association of copy number variation of the 15q11.2 BP1-BP2 region with cortical and subcortical morphology and cognition. JAMA Psychiatry. 2019;77:1–11. 86. Maillard AM, Ruef A, Pizzagalli F, Migliavacca E, Hippolyte L, Adaszewski S, et al. The 16p11.2 locus modulates brain structures...
PCR-Based Detection of DNA Copy Number Variation 来自 Springer 喜欢 0 阅读量: 31 作者: M Mehrotra 摘要: Copy number variations are important polymorphisms that can influence gene expression within and close to the rearranged region, and results in phenotypic variation. Techniques that detect ...
(National Center for Biotechnology Journal of Human Genetics CNVs in XLMR S Honda et al 592 Information, http://www.ncbi.nlm.nih.gov/) and not registered in the Database of Genomic Variants (DGVs, http://projects.tcag.ca/ variation/) in the male proband, we examined other family ...
15. Zhang ZD, Gerstein MB: Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model. BMC ... ZD Zhang,J Du,H Lam,... - 《Bmc Genomics》 被引量: 90发表: 2011年 The Human Genome Diversity Project: A Case Study in Coproduction....