swMATH19390MaRDI QIDQ31217FDOQ31217
Author name not available (Why is that?)
Official website: http://genome.cshlp.org/content/17/11/1665.short
Cited In (30)
- Leveraging local identity-by-descent increases the power of case/control GWAS with related individuals
- Semiparametric hidden Markov model with non-parametric regression
- iBATCGH: integrative Bayesian analysis of transcriptomic and CGH data
- 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
- oligo
- Pedcheck
- BioHMM
- BRLMM
- VanillaICE
- IMPUTE
- CGHclassify
- CNV-seq
- dChipSNP
- PLASQ
- CNVassoc
- iBATCGH
- PICNIC
- COMPADRE
- CARAT
- FASeg
- GenoSNP
- On the accuracy of the MAP inference in HMMs
- Using GWAS data to identify copy number variants contributing to common complex diseases
- Segmentation and estimation for SNP microarrays: A Bayesian multiple change-point approach
- 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
This page was built for software: PennCNV
