FindMaxRepeatIns

Return the number of repeat units in which an insertion
is embedded.

internal

Analysis and visualization of experimentally elucidated mutational
signatures -- the kind of analysis and visualization in Boot et al.,
"In-depth characterization of the cisplatin mutational signature in
human cell lines and in esophageal and liver tumors", Genome Research 2018,
<doi:10.1101/gr.230219.117> and
"Characterization of colibactin-associated mutational signature in an
Asian oral squamous cell carcinoma and in other mucosal tumor types",
Genome Research 2020 <doi:10.1101/gr.255620.119>.
'ICAMS' stands for In-depth Characterization
and Analysis of Mutational Signatures. 'ICAMS' has functions to read in
variant call files (VCFs) and to collate the corresponding catalogs of
mutational spectra and to analyze and plot catalogs of mutational spectra
and signatures. Handles both "counts-based" and "density-based" (i.e.
representation as mutations per megabase) mutational spectra or signatures.

Steve Rozen

ICAMS

In-Depth Characterization and Analysis of Mutational Signatures
('ICAMS')

FindMaxRepeatIns function

<dl><dt>context</dt>
<dd>A string into which <code>rep.unit.seq</code> was
inserted at position <code>pos</code>.</dd>
<dt>rep.unit.seq</dt>
<dd>The inserted sequence and candidate repeat unit
sequence.</dd>
<dt>pos</dt>
<dd><code>rep.unit.seq</code> is understood to be inserted between
positions <code>pos</code> and <code>pos + 1</code>.</dd></dl>

Arguments

Return the number of repeat units in which an insertion
is embedded. — FindMaxRepeatIns

<dl>

<dt>context</dt>
<dd>A string into which <code>rep.unit.seq</code> was
inserted at position <code>pos</code>.</dd>


<dt>rep.unit.seq</dt>
<dd>The inserted sequence and candidate repeat unit
sequence.</dd>


<dt>pos</dt>
<dd><code>rep.unit.seq</code> is understood to be inserted between
positions <code>pos</code> and <code>pos + 1</code>.</dd>

</dl>

FindMaxRepeatIns: Return the number of repeat units in which an insertion is embedded.

Description

Usage

Value

Arguments

Details