PennCNV
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swMATH19390MaRDI QIDQ31217FDOQ31217
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Cited In (13)
- Leveraging local identity-by-descent increases the power of case/control GWAS with related individuals
- Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change-Point Approach
- Semiparametric hidden Markov model with non-parametric regression
- PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data
- iBATCGH: Integrative Bayesian Analysis of Transcriptomic and CGH Data
- On the accuracy of the MAP inference in HMMs
- Using GWAS data to identify copy number variants contributing to common complex diseases
- A Coarse-to-Fine Approach to Computing the k-Best Viterbi Paths
- The screening and ranking algorithm to detect DNA copy number variations
- Fast estimation of posterior probabilities in change-point analysis through a constrained hidden Markov model
- Detecting simultaneous variant intervals in aligned sequences
- A hierarchical Bayesian model for inference of copy number variants and their association to gene expression
- Reconstructing DNA copy number by penalized estimation and imputation
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