View source: R/RegressHaplo_workflow.R
read_table_to_loci.pipeline | R Documentation |
Given a read table, split variable positions into loci
read_table_to_loci.pipeline(out_dir, max_num_haplotypes = 1200)
out_dir |
output directory for parameter files and assumed directory of read table |
max_num_haplotypes |
the maximum number of haplotypes over the full reference that will be considered. |
The read table is assumed to be in out_dir with filename read_table.csv. The parameter min_cover can (and should) be used to force loci to break across low coverage regions of the reference.
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