Reference-free method for conducting EWAS while deconvoluting DNA methylation
arising as mixtures of cell types.  The older method
(Houseman et al., 2014,<doi:10.1093/bioinformatics/btu029>) is similar to
surrogate variable analysis (SVA and ISVA), except that it makes additional use
of a biological mixture assumption.
The newer method (Houseman et al., 2016, <doi:10.1186/s12859-016-1140-4>) is similar
to non-negative matrix factorization, with additional constraints
and additional utilities.

EWAS using Reference-Free DNA Methylation Mixture Deconvolution

package-ubuntu-20.04-r-4.0.5#cran#RefFreeEWAS-2.2

<p>Print method for objects of type BootRefFreeEwasModel
</p>

## S3 method for class 'BootRefFreeEwasModel'
print(x,...)

<table summary="R argblock">
<tr valign="top">
<td><code>x</code></td>
<td>
<p>BootRefFreeEwasModel object to print</p>
</td>
</tr>
<tr valign="top">
<td><code>...</code></td>
<td>
<p>(Unused).</p>
</td>
</tr>
</table>

<p>See <code><a href="RefFreeEwasModel.html">RefFreeEwasModel</a></code> for example.
</p>

package-ubuntu-20.04-r-4.0.5#cran#RefFreeEWAS-2.2#docs#print.BootRefFreeEwasModel

print.BootRefFreeEwasModel

Description

Usage

Arguments

Details

RefFreeEWAS

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`x`	BootRefFreeEwasModel object to print
`...`	(Unused).