create_chrom_map: Create chromosome map from marker map
In SimRVSequences: Simulate Genetic Sequence Data for Pedigrees
Description
Usage
Arguments
Value
View source: R/marker_map_functions.R
Description
INTENDED FOR INTERNAL USE ONLY
Usage
1
create_chrom_map(SNV_map)
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.
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Description Usage Arguments Value
View source: R/marker_map_functions.R
Description
INTENDED FOR INTERNAL USE ONLY
Usage
1 | create_chrom_map(SNV_map)
|
Arguments
SNV_map |
Data frame. A data frame that catalogs the SNVs in |
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.
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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