f π |
0.1,0.7 |
Vector of length J of initial sample fractions. Default assumes two samples, with low and high tumor content. |
απ |
1.5 |
Determines shape of prior distribution of Δf |
π (N = 0) …π (N = 3), π (N ≥ 5) |
0.01,0.25,0.3,0.2,0.15,0.09 |
Copy Number Priors |
π (M = 0), π (M = 1), π (M ≥ 2) |
0.25,0.5,0.25 |
Minor Allele Copy Number Priors |
αseg |
1E-5 |
Segmentation significance cutoff |
ω |
COSMIC |
Number of cancer variants observed at the position |
FA, FB
|
1,000 Genomes and Exac |
Population Allele Frequencies |
ρSNV, ρindel
|
1E-5, 1E-6 |
Constant for calculating prior somatic |
Fp−SNV, Fp−indel
|
1E-5, 1E-6 |
Population allele frequencies assigned to alleles not seen in input population |
Fmax−somatic
|
2E-5 |
Maximum population allele frequency to be considered a possible somatic variant |
|
10 |
Minimum mapping quality to count read |
|
5 |
Minimum base quality to count base |
T PASS |
0.8 |
Minimum posterior probability of belonging to the PASS group to be called pass |
T Somatic |
0.8 |
Minimum posterior probability of variant is somatic to be called somatic |
T Germline |
0.8 |
Minimum posterior probability of variant is germline to be called germline |
ξ |
3 |
Number of parameter fitting iterations without new global minimum before stopping |
λ |
5 |
Weight of penalty for adding clonal variant group |