Bayesian hidden Markov models to identify RNA–protein interaction sites in PAR‐CLIP

J Yun, T Wang, G Xiao - Biometrics, 2014 - Wiley Online Library
The photoactivatable ribonucleoside enhanced cross‐linking immunoprecipitation (PAR‐
CLIP) has been increasingly used for the global mapping of RNA–protein interaction sites …

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 …

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 …

Statistical considerations on NGS data for inferring copy number variations

J Chen - Deep Sequencing Data Analysis, 2021 - Springer
The next-generation sequencing (NGS) technology has revolutionized research in genetics
and genomics, resulting in massive NGS data and opening more fronts to answer …

A Bayesian integrative model for genetical genomics with spatially informed variable selection

A Cassese, M Guindani, M Vannucci - Cancer informatics, 2014 - journals.sagepub.com
We consider a Bayesian hierarchical model for the integration of gene expression levels
with comparative genomic hybridization (CGH) array measurements collected on the same …

MSMAD: a computationally efficient method for the analysis of noisy array CGH data

E Budinska, E Gelnarova, MG Schimek - Bioinformatics, 2009 - academic.oup.com
Motivation: Genome analysis has become one of the most important tools for understanding
the complex process of cancerogenesis. With increasing resolution of CGH arrays, the …

Statistical models for DNA copy number variation detection using read‐depth data from next generation sequencing experiments

T Ji, J Chen - Australian & New Zealand Journal of Statistics, 2016 - Wiley Online Library
Summary In this 'Big Data'era, statisticians inevitably encounter data generated from various
disciplines. In particular, advances in bio‐technology have enabled scientists to produce …

[PDF][PDF] Clinical and genomic strategies for detecting hepatocellular carcinoma in early stages: a systematic review

EM Hashem, MS Mabrouk, AM Eldeib - Am J Biomed Eng, 2015 - researchgate.net
Hepatocellular carcinoma is one of the commonest deadly tumors, and it is usually diagnose
at a late stage, when effective treatment is very difficult. Making its discovery before the …

A latent class model with hidden markov dependence for array cgh data

SM DeSantis, EA Houseman, BA Coull, DN Louis… - …, 2009 - academic.oup.com
Array CGH is a high-throughput technique designed to detect genomic alterations linked to
the development and progression of cancer. The technique yields fluorescence ratios that …

Robust hidden semi-Markov modeling of array CGH data

J Ding, SP Shah - 2010 IEEE International Conference on …, 2010 - ieeexplore.ieee.org
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 …