PennCNV
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Related Items (13)
Fast estimation of posterior probabilities in change-point analysis through a constrained hidden Markov model ⋮ On the accuracy of the MAP inference in HMMs ⋮ Semiparametric hidden Markov model with non-parametric regression ⋮ Leveraging local identity-by-descent increases the power of case/control GWAS with related individuals ⋮ iBATCGH: Integrative Bayesian Analysis of Transcriptomic and CGH Data ⋮ Using GWAS data to identify copy number variants contributing to common complex diseases ⋮ Detecting simultaneous variant intervals in aligned sequences ⋮ A hierarchical Bayesian model for inference of copy number variants and their association to gene expression ⋮ PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data ⋮ A Coarse-to-Fine Approach to Computing the k-Best Viterbi Paths ⋮ Reconstructing DNA copy number by penalized estimation and imputation ⋮ The screening and ranking algorithm to detect DNA copy number variations ⋮ Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change-Point Approach
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