run_hatchet | R Documentation |
Preprocess sequencing data
run_hatchet(
tumour = NULL,
normal = NULL,
chromosomes = NULL,
env_hatchet = build_default_python_enviroment_list()$env_hatchet,
config = build_default_hatchet_config(),
ref_genome = build_default_reference_list()$HG19$reference$genome,
...
)
tumour |
Path to a single or multiple BAM files |
normal |
Path to a normal matched BAM file |
chromosomes |
Select chromosomes to analyze. Default NULL |
env_hatchet |
Hatchet conda enviroment |
config |
Hatchet configuration for each step |
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