Description Usage Arguments Examples
View source: R/variantCalling.R
Tumor-normal pair somatic variant calling using RADIA
1 2 3 4 5 6 7 8 9 10 11 12 | radiaCalling(
tumor_file,
normal_file,
sample_name,
ref,
out_path,
radia_path,
python_radia,
samtools,
threads,
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. |
python_radia |
Path to the python binary with all the RADIA prerequisites. |
samtools |
Path of samtools binary. |
threads |
Number of threads to use in the analysis. |
1 2 3 4 5 6 7 8 9 10 11 | ## Not run:
radiaCalling(tumor_file = 'raw/sample_tumor.bam',
normal_file = 'raw/sample_normal.bam',
sample_name = 'sample'
ref = 'ref/hg38.fa',
out_path = 'rst',
radia_path = '/bin/radia/scripts',
python_radia = 'venv/radia/bin/python',
samtools = '/bin/samtools')
## End(Not run)
|
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