Description Usage Arguments Examples
View source: R/variantCalling.R
Tumor-normal pair somatic variant calling using SomaticSniper
1 2 3 4 5 6 7 8 9 10 11 | somaticsniperCalling(
tumor_file,
normal_file,
sample_name,
ref,
out_path,
somatic_sniper,
fpfilter,
perl,
bcftools
)
|
tumor_file |
Tumor bam to file to perform the variant calling. |
normal_file |
Normal bam to file to perform the variant calling. |
ref |
Path for the reference genome to use for the alignment (fasta format) and the corresponding indexes generated with bwa index and a dictionary index file generated by CreateSequenceDictionary gatk tool. |
out_path |
Path where the output of the analysis will be saved. |
somatic_sniper |
Path of SomaticSniper binary. |
perl |
Path of perl executable. |
1 2 3 4 5 6 7 8 9 | ## Not run:
somaticsniperCalling(tumor_file = 'raw/sample_tumor.bam',
normal_file = 'raw/sample_normal.bam',
sample_name = 'sample'
ref = 'ref/hg38.fa',
out_path = 'rst',
somatic_sniper = '/bin/bam-somaticsniper')
## End(Not run)
|
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