Recursive HMM to identify CNV boundaries using allele data
r.sub |
Optional matrix of alt allele count in single cells. If not provided, internal r.sc matrix is used. |
n.sub |
Optional matrix of site coverage count in single cells. If not provided, internal n.sc matrix is used. |
l.sub |
Optional vector of alt allele count in pooled single cells or bulk. If not provided, internal l vector is used. |
n.bulk.sub |
Optional vector of site coverage count in pooled single cells or bulk. If not provided, internal n.bulk vector is used. |
min.traverse |
Depth traversal to look for subclonal CNVs. Higher depth, potentially smaller subclones detectable. (default: 3) |
t |
HMM transition parameter. Higher number, more transitions. (default: 1e-6) |
pd |
Probability of lesser allele detection in deleted region (ie. due to error) |
pn |
Probability of lesser allele detection in neutral region (ie. 0.5 - error rate) |
min.num.snps |
Minimum number of snps in candidate CNV |
trim |
Trim boundary SNPs |
init |
Boolean whether to initialize |
verbose |
Verbosity(default: FALSE) |
... |
Additional parameters to pass to calcAlleleCnvProb |
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