create_chrom_map

<p>Data frame. A data frame that catalogs the SNVs in <code>haplos</code>.  If the <code><a rd-options="" href="/link/read_slim?package=SimRVSequences&version=0.2.7" data-mini-rdoc="SimRVSequences::read_slim">read_slim</a></code> function was used to import SLiM data to <code>R</code>, the data frame <code>Mutations</code> is of the proper format for <code>SNV_map</code>.  However, users must add the variable <code>is_CRV</code> to this data frame, see details.</p>

SNV_map

internal

Methods to simulate genetic sequence data for pedigrees, with
functionality to simulate genetic heterogeneity among pedigrees.
Christina Nieuwoudt, Angela Brooks-Wilson,
and Jinko Graham (2019) <doi:10.1101/534552>.

Christina Nieuwoudt

SimRVSequences

Simulate Genetic Sequence Data for Pedigrees

Jinko Graham

create_chrom_map function

<p>Data frame. A data frame that catalogs the SNVs in <code>haplos</code>.  If the <code><a rd-options='' href='read_slim'>read_slim</a></code> function was used to import SLiM data to <code>R</code>, the data frame <code>Mutations</code> is of the proper format for <code>SNV_map</code>.  However, users must add the variable <code>is_CRV</code> to this data frame, see details.</p>

create_chrom_map: Create chromosome map from marker map

Description

Usage

Arguments

Value