In this thesis, a multifactor dimensionality reduction based method on associative classification is employed to identify higher-order SNP interactions for enhancing the understanding of the genetic architecture of complex diseases. Further, this thesis explored the application of deep learning techniques by providing new clues into the interaction analysis. The performance of the deep learning method is maximized by unifying deep neural networks with a random forest for achieving reliable interactions in the presence of noise
The genetic epidemiology behind the complex diseases are characterised by multiple factors acting to...
We show that by representing Single Nucleotide Polymorphism (SNP) data to a neural network in a way ...
The study of Single Nucleotide Polymorphisms (SNPs) associated with human diseases is important for...
There have been many studies that depict genotype phenotype relationships by identifying genetic var...
The complexity of phenotype-genotype mapping are characterised by non-linear interactions between ge...
The susceptibility of complex diseases are characterised by numerous genetic, lifestyle, and environ...
The extent to which genetic interactions affect observed phenotypes is generally unknown because cur...
Revealing the underlying complex architecture of human diseases has received considerable attention ...
In this era of genome-wide association studies (GWAS), the quest for understanding the genetic archi...
Identification and characterization of interactions between genes have been increasingly explored in...
The complexity of phenotype-genotype mapping are characterised by non-linear interactions between ge...
Funding Information: The work used computer resources of the Aalto University School of Science Scie...
Background. As time passes, the field of biology is constantly revolutionised by the rapid emergence...
<div><p>Single Nucleotide Polymorphisms (SNPs) found in Genome-Wide Association Study (GWAS) mainly ...
Single Nucleotide Polymorphisms (SNPs) found in Genome-Wide Association Study (GWAS) mainly influenc...
The genetic epidemiology behind the complex diseases are characterised by multiple factors acting to...
We show that by representing Single Nucleotide Polymorphism (SNP) data to a neural network in a way ...
The study of Single Nucleotide Polymorphisms (SNPs) associated with human diseases is important for...
There have been many studies that depict genotype phenotype relationships by identifying genetic var...
The complexity of phenotype-genotype mapping are characterised by non-linear interactions between ge...
The susceptibility of complex diseases are characterised by numerous genetic, lifestyle, and environ...
The extent to which genetic interactions affect observed phenotypes is generally unknown because cur...
Revealing the underlying complex architecture of human diseases has received considerable attention ...
In this era of genome-wide association studies (GWAS), the quest for understanding the genetic archi...
Identification and characterization of interactions between genes have been increasingly explored in...
The complexity of phenotype-genotype mapping are characterised by non-linear interactions between ge...
Funding Information: The work used computer resources of the Aalto University School of Science Scie...
Background. As time passes, the field of biology is constantly revolutionised by the rapid emergence...
<div><p>Single Nucleotide Polymorphisms (SNPs) found in Genome-Wide Association Study (GWAS) mainly ...
Single Nucleotide Polymorphisms (SNPs) found in Genome-Wide Association Study (GWAS) mainly influenc...
The genetic epidemiology behind the complex diseases are characterised by multiple factors acting to...
We show that by representing Single Nucleotide Polymorphism (SNP) data to a neural network in a way ...
The study of Single Nucleotide Polymorphisms (SNPs) associated with human diseases is important for...