BioHMM
From MaRDI portal
Cited in
(21)- Fast estimation of posterior probabilities in change-point analysis through a constrained hidden Markov model
- Sparse latent factor models with interactions: analysis of gene expression data
- A hierarchical Bayesian model for inference of copy number variants and their association to gene expression
- CGHclassify
- CNV-seq
- Segmentation and estimation for SNP microarrays: A Bayesian multiple change-point approach
- CNVassoc
- PennCNV
- PICNIC
- A continuous-index hidden Markov jump process for modeling DNA copy number data
- A shifting level model algorithm that identifies aberrations in array-CGH data
- TigrScan
- GlimmerHMM
- COMPADRE
- WBDev
- A decision-theoretic approach for segmental classification
- Modeling read counts for CNV detection in exome sequencing data
- ExomeCNV
- CARAT
- A Bayesian HMM with random effects and an unknown number of states for DNA copy number analysis
- A latent class model with hidden Markov dependence for array CGH data
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