Array comparative genomic hybridization (aCGH) is one of the techniques that can be used to detect copy number variations in DNA sequences in high resolution. It has been identified that abrupt changes in the human genome play a vital role in the progression and development of many complex diseases. In this study we propose two distinct hybrid algorithms that combine efficient sequential change-point detection procedures (the Shiryaev-Roberts procedure and the cumulative sum control chart (CUSUM) procedure) with the Cross-Entropy method, which is an evolutionary stochastic optimization technique to estimate both the number of change-points and their corresponding locations in aCGH data. The proposed hybrid algorithms are applied to both art...
We model DNA count data as a multiple change point problem, in which the data are divided in to diff...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...
Array comparative genomic hybridization (aCGH) is one of the techniques that can be used to detect c...
Array comparative genomic hybridization (aCGH) is one of the techniques that can be used to detect c...
Thesis by publication.Spine title: The CE method and multiple change-point detection.Includes biblio...
Array comparative genome hybridization (aCGH) is a widely used methodology to detect copy number var...
Array comparative genome hybridization (aCGH) is a widely used methodology to detect copy number var...
Genomes of eukaryotic organisms vary in GC ratio, that is, share of DNA bases such that C or G as co...
Genome research is one of the most interesting and important areas of the science nowadays. It is we...
It is well-known that many genomes are highly structured. So determining domains of similar pattern ...
Detection and characterization of genomic structural variations are essential in identifying disease...
The genomes of complex organisms, including the human genome, are known to vary in GC content along ...
The genomes of complex organisms, including the human genome, are known to vary in GC content along ...
We model DNA count data as a multiple change point problem, in which the data are divided in to diff...
We model DNA count data as a multiple change point problem, in which the data are divided in to diff...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...
Array comparative genomic hybridization (aCGH) is one of the techniques that can be used to detect c...
Array comparative genomic hybridization (aCGH) is one of the techniques that can be used to detect c...
Thesis by publication.Spine title: The CE method and multiple change-point detection.Includes biblio...
Array comparative genome hybridization (aCGH) is a widely used methodology to detect copy number var...
Array comparative genome hybridization (aCGH) is a widely used methodology to detect copy number var...
Genomes of eukaryotic organisms vary in GC ratio, that is, share of DNA bases such that C or G as co...
Genome research is one of the most interesting and important areas of the science nowadays. It is we...
It is well-known that many genomes are highly structured. So determining domains of similar pattern ...
Detection and characterization of genomic structural variations are essential in identifying disease...
The genomes of complex organisms, including the human genome, are known to vary in GC content along ...
The genomes of complex organisms, including the human genome, are known to vary in GC content along ...
We model DNA count data as a multiple change point problem, in which the data are divided in to diff...
We model DNA count data as a multiple change point problem, in which the data are divided in to diff...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...
Motivation: Knowing the exact locations of multiple change points in genomic sequences serves severa...