Results 161 to 170 of about 27,549 (205)
Haplotype applications in genomic selection. [PDF]
MacNish TR, Bergmann T, Edwards D.
europepmc +1 more source
On the limits of detection of epistatic higher-order interactions
Camacho-Mateu J +4 more
europepmc +1 more source
Epistasis and the changing fitness landscapes of SARS-CoV-2
Sesta L, Neher RA.
europepmc +1 more source
Since Bateson's discovery that genes can suppress the phenotypic effects of other genes, gene interactions—called epistasis—have been the topic of a vast research effort. Systems and developmental biologists study epistasis to understand the genotype–phenotype map, whereas evolutionary biologists recognize the fundamental importance of epistasis for ...
Timothy Cooper +2 more
exaly +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Dynamics in Epistasis Analysis
IEEE/ACM Transactions on Computational Biology and Bioinformatics, 2018Finding regulatory relationships between genes, including the direction and nature of influence between them, is a fundamental challenge in the field of molecular genetics. One classical approach to this problem is epistasis analysis. Broadly speaking, epistasis analysis infers the regulatory relationships between a pair of genes in a genetic pathway ...
Aseel Awdeh +3 more
openaire +2 more sources
Symbolic Modeling of Epistasis
Human Heredity, 2007The workhorse of modern genetic analysis is the parametric linear model. The advantages of the linear modeling framework are many and include a mathematical understanding of the model fitting process and ease of interpretation. However, an important limitation is that linear models make assumptions about the nature of the data being modeled.
Jason H, Moore +5 more
openaire +2 more sources
Epistasis in Neuropsychiatric Disorders
Trends in Genetics, 2017The contribution of epistasis to human disease remains unclear. However, several studies have now identified epistatic interactions between common variants that increase the risk of a neuropsychiatric disorder, while there is growing evidence that genetic interactions contribute to the pathogenicity of rare, multigenic copy-number variants (CNVs) that ...
openaire +2 more sources

