This function calls structural variants in a pair of tumor-normal or in single tumor/normal samples matched samples using svaba
1 2 3 4 5 6 7 8 9 10 11 12 13 14 | call_sv_svaba(
tumor_bam = "",
bin_path = "tools/svaba/bin/svaba",
bin_path2 = "tools/htslib/bgzip",
bin_path3 = "tools/htslib/tabix",
normal_bam = "",
ref_genome = "",
threads = 3,
output_name = "",
targets = "",
dbsnp_indels = "",
verbose = FALSE,
output_dir = ""
)
|
tumor_bam |
REQUIRED Path to tumor bam file. |
bin_path |
REQUIRED Path to svaba binary executable. Default path tools/svaba/svaba. |
bin_path2 |
REQUIRED Path to bgzip binary executable. Default path tools/htslib/bgzip. |
bin_path3 |
REQUIRED Path to tabix binary executable. Default path tools/htslib/tabix. |
normal_bam |
OPTIONAL Path to germline bam file. |
ref_genome |
REQUIRED Path to reference genome fasta file. |
threads |
OPTIONAL Number of threads to use. Default 3. |
output_name |
OPTIONAL Name for the output. |
targets |
OPTIONAL BED file with capture target regions. |
dbsnp_indels |
OPTIONAL Database with indel annotations. |
verbose |
OPTIONAL Enables progress messages. Default False. |
output_dir |
OPTIONAL Path to the output directory. |
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