This function calls variants in a sample.
1 2 3 4 5 6 7 8 | vcf_bcftools(
region = "",
bin_path = "tools/bcftools/bcftools",
bam = "",
ref_genome = "",
output_dir = "",
verbose = FALSE
)
|
region |
Region to analyze. Optional |
bin_path |
Path to fastQC executable. Default path tools/gatk/gatk. |
bam |
Path to bam file. |
ref_genome |
Path to reference genome fasta file. |
output_dir |
Path to the output directory. |
verbose |
Enables progress messages. Default False. |
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