Results 261 to 270 of about 1,217,732 (304)

Copy Number Variation Shapes Structural Genomic Diversity Associated With Ecological Adaptation in the Wild Tomato Solanum chilense. [PDF]

Mol Biol Evol
Wei K, Stam R, Tellier A, Silva-Arias GA.   +3 more
europepmc   +1 more source

The role of AMY1 gene copy number variation in dental caries susceptibility: insights from a Turkish population. [PDF]

BMC Oral Health
Hatipoğlu Ö, Saydam F.
europepmc   +1 more source

Analysis of sequence-based copy number variation detection tools for cancer studies [PDF]

, 2014
Cai, Zhengqiu, Nabavi, Sheida, Tonellato, Peter J   +2 more
core  

A benchmarking study of copy number variation inference methods using single-cell RNA-sequencing data. [PDF]

Precis Clin Med
Chen X, Fang LT, Chen Z, Chen W, Wu H, Zhu B, Moos M, Farmer A, Zhang X, Xiong W, Gong S, Jones W, Mason CE, Wu S, Xiao C, Wang C.   +15 more
europepmc   +1 more source

Detection of <i>Ureaplasma parvum</i> in amniotic fluids via reanalysis of prenatal copy number variation sequencing data: an exploratory study. [PDF]

Front Cell Infect Microbiol
Wang G, Chen W, Chen X, Hou H, Zhang J, Han Z.   +5 more
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

Copy-number variation

Nature Reviews Microbiology, 2020
This study reports that extensive copy number variations occur in the presence of azole antifungal drugs in Candida albicans, which might cause phenotypic and population-level heterogeneity observed in clinical isolates.
A. Jeremy Willsey, Montana T. Morris
exaly   +5 more sources

Copy Number Variation

2018
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversions and copy number variants (CNVs, gain or loss of DNA). The latter can range from sub-microscopic events to complete chromosomal aneuploidies. Small CNVs are often benign but those larger than 250 kb are strongly associated with morbid consequences ...
Aurélien, Macé, Zoltán, Kutalik, Armand, Valsesia   +2 more
openaire   +3 more sources

Copy Number Variation

2010
Recent genetic epidemiology studies have been dominated by genome-wide association (GWA) studies using single nucleotide polymorphisms (SNPs). However, a form of structural genomic variation, termed copy number variation (CNV), is also widespread throughout the human genome, and can be highly polymorphic between individuals.
Wain, LV, Tobin, MD
openaire   +3 more sources