Frequencies for 22 loci from the prototype 24-plex STR panel from Thermo Fisher.

datasets

Analysis of DNA mixtures involving relatives by computation of likelihood ratios that account for dropout and drop-in, mutations, silent alleles and population
substructure. This is useful in kinship cases, like non-invasive prenatal paternity testing, where deductions about individuals' relationships rely on DNA mixtures,
and in criminal cases where the contributors to a mixed DNA stain may be related. Relationships are represented
by pedigrees and can include kinship between more than two individuals. The main function is relMix() and its graphical user interface relMixGUI().
The implementation and method is described in Dorum et al. (2017) <doi:10.1007/s00414-016-1526-x>, Hernandis et al. (2019)
<doi:10.1016/j.fsigss.2019.09.085> and Kaur et al. (2016) <doi:10.1007/s00414-015-1276-1>.

Guro Dorum

relMix

Relationship Inference for DNA Mixtures

Elias Hernandis

Navreet Kaur

Thore Egeland

Magnus Dehli Vigeland

db2 function

A data frame with 206 observations on the following 3 variables.<dl>
 <dt><code>Marker</code></dt>
<dd>a factor with levels corresponding to name of markers</dd> <dt><code>Allele</code></dt>
<dd>a numeric vector denoting allele</dd> <dt><code>Frequency</code></dt>
<dd>a numeric vector in (0,1)</dd></dl>

Format

Allele database for 22 markers — db2

A data frame with 206 observations on the following 3 variables.<dl>
 <dt><code>Marker</code></dt>
<dd>a factor with levels corresponding to name of markers</dd>

 <dt><code>Allele</code></dt>
<dd>a numeric vector denoting allele</dd>

 <dt><code>Frequency</code></dt>
<dd>a numeric vector in (0,1)</dd>

</dl>

db2: Allele database for 22 markers

Description

Usage

Arguments

Format

Details

Examples