Description Usage Arguments Details Value
View source: R/Read_SBS_VCF_and_BAMs_to_verify_DBSs.R
Aggressively merge SBSs into DBSs then determine whether sequencing reads in fact support DBSs.
1 2 3 4 5 6 7 8 9 10 11 | Read_SBS_VCF_and_BAMs_to_verify_DBSs(
input.vcf,
Nbam.name,
Tbam.name,
variant.caller,
N.slice.dir = tempfile(),
T.slice.dir = tempfile(),
unlink.slice.dir = TRUE,
outfile = NULL,
verbose = 0
)
|
input.vcf |
If a character string, then the path to a VCF file; otherwise A a single VCF "file" as a data.frame or similar object. |
Nbam.name |
The name of the BAM file for the normal sample corresponding to |
Tbam.name |
The name of the BAM file for the tumor sample corresponding to |
variant.caller |
One of |
N.slice.dir |
Directory for the slices of the normal BAM. Created if necessary. |
T.slice.dir |
Directory for the slices of the tumor BAM.
Created if necessary. Must be different than |
unlink.slice.dir |
If |
outfile |
If not |
verbose |
If > 0 print a message when starting the number of slices
generated every |
Note: argument input.vcf
must be a file path.
This function creates a new VCF file.
See Read_DBS_VCF_and_BAMs_to_verify_DBSs
for details.
Same as Read_DBS_VCF_and_BAMs_to_verify_DBSs
.
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