Detecting simultaneous changepoints in multiple sequences
We discuss the detection of local signals that occur at the same location in multiple one-
dimensional noisy sequences, with particular attention to relatively weak signals that may …
dimensional noisy sequences, with particular attention to relatively weak signals that may …
DNA copy number profiling in normal and tumor genomes
NR Zhang - Frontiers in Computational and Systems Biology, 2010 - Springer
For a biological sample, the DNA copy number of a genomic region is defined as the
number of copies of the DNA in that region within the genome of the sample, relative to …
number of copies of the DNA in that region within the genome of the sample, relative to …
Bayesian random segmentation models to identify shared copy number aberrations for array CGH data
Array-based comparative genomic hybridization (aCGH) is a high-resolution, high-
throughput technique for studying the genetic basis of cancer. The resulting data consist of …
throughput technique for studying the genetic basis of cancer. The resulting data consist of …
Robust unmixing of tumor states in array comparative genomic hybridization data
D Tolliver, C Tsourakakis, A Subramanian… - …, 2010 - academic.oup.com
Motivation: Tumorigenesis is an evolutionary process by which tumor cells acquire
sequences of mutations leading to increased growth, invasiveness and eventually …
sequences of mutations leading to increased growth, invasiveness and eventually …
Sticky hidden Markov modeling of comparative genomic hybridization
We develop a sticky hidden Markov model (HMM) with a Dirichlet distribution (DD) prior,
motivated by the problem of analyzing comparative genomic hybridization (CGH) data. As …
motivated by the problem of analyzing comparative genomic hybridization (CGH) data. As …
Posterior simulation in countable mixture models for large datasets
S Guha - Journal of the American Statistical Association, 2010 - Taylor & Francis
Mixture models, or convex combinations of a countable number of probability distributions,
offer an elegant framework for inference when the population of interest can be subdivided …
offer an elegant framework for inference when the population of interest can be subdivided …
Detecting copy number variations from array CGH data based on a conditional random field model
XL Yin, J Li - Journal of bioinformatics and computational biology, 2010 - World Scientific
Array comparative genomic hybridization (aCGH) allows identification of copy number
alterations across genomes. The key computational challenge in analyzing copy number …
alterations across genomes. The key computational challenge in analyzing copy number …
Integrative classification and analysis of multiple arrayCGH datasets with probe alignment
Z Tian, R Kuang - Bioinformatics, 2010 - academic.oup.com
Motivation: Array comparative genomic hybridization (arrayCGH) is widely used to measure
DNA copy numbers in cancer research. ArrayCGH data report log-ratio intensities of …
DNA copy numbers in cancer research. ArrayCGH data report log-ratio intensities of …
Robust hidden semi-Markov modeling of array CGH data
As an extension to hidden Markov models, the hidden semi-Markov models allow the
probability distribution of staying in the same state to be a general distribution. Therefore …
probability distribution of staying in the same state to be a general distribution. Therefore …
Segmentation and estimation for SNP microarrays: A Bayesian multiple change-point approach
YC Tai, MN Kvale, JS Witte - Biometrics, 2010 - academic.oup.com
High-density single-nucleotide polymorphism (SNP) microarrays provide a useful tool for the
detection of copy number variants (CNVs). The analysis of such large amounts of data is …
detection of copy number variants (CNVs). The analysis of such large amounts of data is …