Bayesian hidden Markov models to identify RNA–protein interaction sites in PAR‐CLIP
The photoactivatable ribonucleoside enhanced cross‐linking immunoprecipitation (PAR‐
CLIP) has been increasingly used for the global mapping of RNA–protein interaction sites …
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 …
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 …
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 …
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
We consider a Bayesian hierarchical model for the integration of gene expression levels
with comparative genomic hybridization (CGH) array measurements collected on the same …
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 …
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
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 …
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
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 …
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
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 …
the development and progression of cancer. The technique yields fluorescence ratios that …
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 …