DMRViterbi {DMRMark} | R Documentation |

This function takes M-values and estimated parameters from 'DMRMark', then uses Viterbi algorithm for estimating states' posterior probabilities for each locus.

DMRViterbi(mv, pars, L = rep(1, nrow(mv)), starting = NULL, pd = NULL, region = TRUE, orderBy = c("max", "mean", "median", "min"), VitP = NULL)

`mv` |
The input M-values matrix, NA is not allowed. |

`pars` |
The list of model parameters. Getting by calling 'DMRMark'. |

`L` |
A vector to specify the distance between each probes in bp. $L < 0$ represents change of chromosome. Default is $L = 1$ for all probes. |

`starting` |
A vector to specify the position to initial new chains. We suggest new chains should be initiated at least at starting of new chromosome. When it is null, new chains initiate at beginning and where $L > 100000 or $L < 0$. |

`pd` |
A design matrix, which can be generated by 'stats::model.matrix'. If the M-values are totally paired or single paired, just leave it to be NULL. |

`region` |
If set to TRUE, this function returns the regions formed by Viterbi posterior states. Otherwise, it returns posterior probabilities and states for individual loci. Default is TRUE. |

`orderBy` |
Only enabled when 'region = TRUE'. Order the regions by which statistics? Choice include 'max', 'mean', 'median' and 'min', which orders the regions by the maximum, geometric mean, median or minimum of the posterior probabilities in each region respectively. Default is 'max'. |

`VitP` |
Only enabled when 'region = FALSE'. The minimum posterior probabilities required to be the DMC states. A locus with DMC's posterior probability lower than 'VitP' will in the non-DMC states with highest probabilities. When set to NULL, simply return the MAP states. Default is NULL. |

If 'region = FALSE', the return value is a list contains:

`states` |
The MAP methylation status satisfies the 'VitP'. |

`deltas` |
The matrix with each row corresponds to the posterior probabilities of each locus in which states. |

If 'region = TRUE', the return value is a dataframe with the following fields:

`begin` |
Beginning of each region. In probe index. |

`ending` |
Ending of each region. In probe index. |

`MAP_state` |
The MAP state of each region. |

`minVP` |
The minimum Viterbi posterior probability of the MAP state in each region |

`meanVP` |
The geometric mean of Viterbi posterior probability of the MAP state in each region |

`maxVP` |
The maximum Viterbi posterior probability of the MAP state in each region |

`midVP` |
The median Viterbi posterior probability of the MAP state in each region |

Linghao SHEN <sl013@ie.cuhk.edu.hk>

See `DMRMark`

about model parameter estimation

# DMRViterbi # DMR detection performed on chr18 of a small BLCA dataset from TCGA data(BLCA) # Use a small subset nprobe <- 500 # M-values mv <- BLCA$mv[1:nprobe,] # Distance between probes, L<0 indicates acorssing chromosomes L = BLCA$distance[1:nprobe] # Initialize new chain when probe distance too long # or across different chromosomes newChains <- which((L > 100000) | L < 0) # The starting positions of new chains starting <- c(1, newChains[-length(newChains)]+1) # Run DMRMark with default options pars <- DMRMark(mv, L, starting) # Get the posterior of being certain states results <- DMRViterbi(mv, pars, L, starting) head(results)

[Package *DMRMark* version 1.1.1 Index]