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<package>
  <name>penncnv</name>
  <version>2009.08.27</version>
  <doc>
    <title>penncnv</title>
    <description>
        <text lang="en"> CNV detection from Illumina whole-genome SNP genotyping arrays. 
          It has been extended to handle candidate gene SNP arrays, to handle recent 
          high-density arrays with non-polymorphic markers (so-called CN markers),
          and to handle Affymetrix genome-wide arrays.</text>
     </description>
     <authors>Wang K</authors>
     <reference>Wang K, Li M, Hadley D, Liu R, Glessner J, Grant S, Hakonarson H, Bucan M. PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genome Research 17:1665-1674, 2007</reference>
     <reference>Diskin SJ, Li M, Hou C, Yang S, Glessner J, Hakonarson H, Bucan M, Maris JM, Wang K. Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms Nucleic Acids Research 36:e126, 2008</reference>
    <reference>Wang K, Chen Z, Tadesse MG, Glessner J, Grant SFA, Hakonarson H, Bucan M, Li M. Modeling genetic inheritance of copy number variations Nucleic Acids Research 36:e138, 2008</reference>
    <homepagelink>http://www.openbioinformatics.org/penncnv/</homepagelink>
    <sourcelink>http://www.openbioinformatics.org/penncnv/penncnv_download.html</sourcelink>
  </doc>
</package>