exons.hg19.X

Exon position extracted from the ensembl database version 61 and on
 chromosome X only.

datasets

Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.

Vincent Plagnol

ExomeDepth

Calls Copy Number Variants from Targeted Sequence Data

exons.hg19.X function

A data frame of exons with the following 4 variables.<dl class="dl-horizontal">
 <dt><code>chromosome</code></dt><dd>a factor with levels <code>X</code> <code>Y</code></dd>
 <dt><code>start</code></dt><dd>a numeric vector</dd>
 <dt><code>end</code></dt><dd>a numeric vector</dd>
 <dt><code>name</code></dt><dd>A character vector of names for the exons</dd>
 </dl>

Format

Positions of exons on build hg19 of the human genome and on chromosome X — exons.hg19.X

A data frame of exons with the following 4 variables.<dl class='dl-horizontal'>
 <dt><code>chromosome</code></dt><dd>a factor with levels <code>X</code> <code>Y</code></dd>
 <dt><code>start</code></dt><dd>a numeric vector</dd>
 <dt><code>end</code></dt><dd>a numeric vector</dd>
 <dt><code>name</code></dt><dd>A character vector of names for the exons</dd>
 </dl>

exons.hg19.X: Positions of exons on build hg19 of the human genome and on chromosome X

Description

Usage

Arguments

Format