Свойство | Тип | Описание | |
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BamPath | string | ||
Chromosome | string | ||
MinimumMapQ | int | ||
OutputPath | string | ||
VcfPath | string |
Метод | Описание | |
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Run ( ) : int | ||
SNVReviewer ( string chromosome, string vcfPath, string bamPath, string outputPath, int minMapQ ) : System |
Метод | Описание | |
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LoadVariants ( string vcfPath ) : void |
Step 1: Load the normal het SNVs of interest.
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ProcessBamFile ( string bamPath ) : void |
Step 2: Get the ref and variant allele frequencies for the variants of interest, in the tumor bam file.
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WriteResults ( string outputPath ) : void |
Step 3: Summarize results to a simple tab-delimited file.
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Метод | Описание | |
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ProcessReadBases ( BamAlignment read, int nextVariantIndex ) : void |
Use the CIGAR string to map bases to chromosome positions, and check whether we see the ref base or the variant allele for our variants of interest.
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protected LoadVariants ( string vcfPath ) : void | ||
vcfPath | string | |
Результат | void |
protected ProcessBamFile ( string bamPath ) : void | ||
bamPath | string | |
Результат | void |
public SNVReviewer ( string chromosome, string vcfPath, string bamPath, string outputPath, int minMapQ ) : System | ||
chromosome | string | |
vcfPath | string | |
bamPath | string | |
outputPath | string | |
minMapQ | int | |
Результат | System |
protected WriteResults ( string outputPath ) : void | ||
outputPath | string | |
Результат | void |