allele under consideration
Map from sequenced bases -> number of reads supporting that allele
Map from allelic mixtures to log10 likelihoods
allele under consideration
allele under consideration
Map from sequenced bases -> number of reads supporting that allele
extra information, including filters, we compute about a potential call
extra information, including filters, we compute about a potential call
Total depth of all reads contributing an allele.
Map from allelic mixtures to log10 likelihoods
Fraction of reads supporting this allele (variant allele frequency).
return a new instance including the given annotations
return a new instance including the given annotations
Summary of evidence for a particular somatic allele in a single tumor RNA sample.
allele under consideration
Map from sequenced bases -> number of reads supporting that allele
Map from allelic mixtures to log10 likelihoods