Segmentation | R Documentation |
If there is no paired normal, other normal sample with the same genome coordinate also works.
Segmentation( Obj_filtered = NULL, raw_counts = NULL, ref_counts = NULL, hmm_states = c(0.5, 1.5, 1.8), hmm_sd = 0.2, hmm_p = 1e-06, nmean = 100, plot_seg = TRUE, rds_path = NULL, adj = 0, max_qt = 0.99 )
Obj_filtered |
An Alleloscope object. |
raw_counts |
A binned coverage matrix (m1 bin by n1 cell) with values being read counts in DNA sequencing data for all chromosomal regions of tumor sample. n1 can be 1 for bulk sample. |
ref_counts |
A binned coverage matrix (m2 bin by n2 cell) with values being read counts in DNA sequencing data for all chromosomal regions of normal sample. n2 can be 1 for bulk sample. Numbers of bins (rows) should be the same in the paired chromosomal regions for the paired samples |
hmm_states |
An ordered vector for the HMM numeric states (deletion, 1-copy gain, 2-copy gains). |
hmm_sd |
Numeric. Fixed standard deviation for the HMM states. |
hmm_p |
Numeric. Transition probability for the HMM algorithm. |
nmean |
Integer. Width of moving window for runmean. |
plot_seg |
Logical (TRUE/ FALSE). Whether or not to plot the segmentation result. |
rds_path |
The path for saving the rds files for the estimated results for each region. |
adj |
Numeric. Value for tumor coverage adjustment. |
max_qt |
Numeric value in 0,1. Setting the maximum value to the max_qt quantile to avoid extreme values. |
A Alleloscope object with "seg_table" added.
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