create_chrom_map: Create chromosome map from marker map

Description Usage Arguments Value

View source: R/marker_map_functions.R

Description

INTENDED FOR INTERNAL USE ONLY

Usage

1

Arguments

SNV_map

Data frame. A data frame that catalogs the SNVs in haplos. If the read_slim function was used to import SLiM data to R, the data frame Mutations is of the proper format for SNV_map. However, users must add the variable is_CRV to this data frame, see details.

Value

a dataframe catalouging the start and stop positions, in base pairs, for each chromosome. We use this information to determine what regions to simulate recombination over.


SimRVSequences documentation built on July 1, 2020, 6:03 p.m.