Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 5.
Figure 5.

Connectivity maps of complex, HPV-associated genomic structural variation in HNSCC cell lines. Schematics of genomic target loci before (top) and after (bottom) HPV integration in HNSCC cell lines (A) UM-SCC-47 and (B) UPCI:SCC090, chromosome 6. Target gene schematic and connectivity map features are as described in the Figure 4 legend. HPV breakpoint numbers are listed in Supplemental Table 3. These schematics including the viral insertions are not drawn to scale. A short inversion in the viral sequence flanking breakpoint 3 is not shown. (Parentheses) Genomic segments with indicated fold amplification (x N) calculated from WGS data; (upside-down letters) inverted segments. See Supplemental Figure 9 for connectivity maps for both UD-SCC-2 and UPCI:SCC090, chromosome 9.

This Article

  1. Genome Res. 24: 185-199

Preprint Server