O'Rawe, Jason, Fang, Han, Rynearson, Shawn, Robison, Reid J., Kiruluta, Edward S., Higgins, Gerald, Eilbeck, Karen, Reese, Martin G., Lyon, Gholson J. (August 2013) Supplemental figure 2 for "Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.". [Image] (Unpublished)
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Abstract
Illumina CLIA Whole genome sequencing data summarized in the form of a Circos plot. We show here a sum-mary of the genomic coordinates corresponding to the 344 genes that were clinically evaluated by the Illumina CLIA WGS pipeline, the frequency of IGN validated SNVs across the genome (plotted in red) and a summary of highly confident copy number variants (CNVs) that were simultaneously detected by the Estimation by Read Depth with SNVs (ERDS) and Copy Number Analysis Method (CNAM) detec-tion methods (plotted in black). Duplications and deletions are depicted as elevations and declinations, respectively.
Item Type: | Image |
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Subjects: | Investigative techniques and equipment Investigative techniques and equipment > assays Investigative techniques and equipment > assays > next generation sequencing Investigative techniques and equipment > assays > whole genome sequencing |
CSHL Authors: | |
Communities: | CSHL labs > Lyon lab |
Depositing User: | Matt Covey |
Date: | 16 August 2013 |
Date Deposited: | 16 Aug 2013 15:18 |
Last Modified: | 16 Aug 2013 15:18 |
URI: | https://repository.cshl.edu/id/eprint/28536 |
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