Pages that link to "Item:Q1876991"

The following pages link to Hidden Markov models approach to the analysis of array CGH data (Q1876991):

Displaying 29 items.

• A model selection approach for multiple sequence segmentation and dimensionality reduction (Q143696) (← links)
• MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts (Q312518) (← links)
• A semiparametric Bayesian model for comparing DNA copy numbers (Q318959) (← links)
• Modeling read counts for CNV detection in exome sequencing data (Q458185) (← links)
• The screening and ranking algorithm to detect DNA copy number variations (Q714382) (← links)
• Using GWAS data to identify copy number variants contributing to common complex diseases (Q908135) (← links)
• Fast estimation of posterior probabilities in change-point analysis through a constrained hidden Markov model (Q1615137) (← links)
• A heuristic, iterative algorithm for change-point detection in abrupt change models (Q1643024) (← links)
• Hidden Markov models for the assessment of chromosomal alterations using high-throughput SNP arrays (Q2271345) (← links)
• Sparse latent factor models with interactions: analysis of gene expression data (Q2443144) (← links)
• A statistical method to detect chromosomal regions with DNA copy number alterations using SNP-array-based CGH data (Q2500263) (← links)
• A Coarse-to-Fine Approach to Computing the k-Best Viterbi Paths (Q3011869) (← links)
• Identification of Differential Aberrations in Multiple-Sample Array CGH Studies (Q3013965) (← links)
• Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change-Point Approach (Q3064251) (← links)
• Detecting Genomic Aberrations Using Products in a Multiscale Analysis (Q3064252) (← links)
• Nonparametric multivariate breakpoint detection for the means, variances, and covariances of a discrete time stochastic process (Q3145403) (← links)
• PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data (Q3303594) (← links)
• A continuous-index hidden Markov jump process for modeling DNA copy number data (Q3305000) (← links)
• A shifting level model algorithm that identifies aberrations in array-CGH data (Q3305020) (← links)
• Bayesian Hidden Markov Modeling of Array CGH Data (Q3632657) (← links)
• A Bayesian HMM with random effects and an unknown number of states for DNA copy number analysis (Q4922611) (← links)
• Prediction in Cancer Genomics Using Topological Signatures and Machine Learning (Q5118370) (← links)
• Bayesian–frequentist hybrid model with application to the analysis of gene copy number changes (Q5124819) (← links)
• Quasi-hidden Markov model and its applications in change-point problems (Q5222477) (← links)
• A Modified Bayes Information Criterion with Applications to the Analysis of Comparative Genomic Hybridization Data (Q5427394) (← links)
• A Segmentation/Clustering Model for the Analysis of Array CGH Data (Q5434903) (← links)
• Multiscale Change Point Inference (Q5743255) (← links)
• A Latent Class Model with Hidden Markov Dependence for Array CGH Data (Q5850980) (← links)
• Moment estimation in discrete shifting level model applied to fast array-CGH segmentation (Q6552759) (← links)