create_chrom_map: Create chromosome map from marker map
In simrvprojects/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.
simrvprojects/SimRVSequences documentation built on March 12, 2020, 1:33 a.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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