Validation of next-generation sequencing for comprehensive chromosome screening of embryos Allen Kung, Santiago Munné, Brandon Bankowski, Alison Coates, Dagan Wells Reproductive BioMedicine Online Volume 31, Issue 6, Pages 760-769 (December 2015) DOI: 10.1016/j.rbmo.2015.09.002 Copyright © 2015 Reproductive Healthcare Ltd. Terms and Conditions
Figure 1 Comparison of a BlueGnome array-comparative genomic hybridization (aCGH) profile to next-generation sequencing (NGS)-produced Integrated Genome Viewer (IGV) profile. An example of a blastocyst sample processed using both aCGH and NGS (Illumina microarrays and the Ion Torrent PGM). The upper panel is the graphical visualization of the NGS analysis using IGV. The lower panel is the graphical representation of the array profile. Both samples presented are scored as an XY, monosomy 4, 11, and a partial monosomy on chromosome 13 from q21.32 to q34. Reproductive BioMedicine Online 2015 31, 760-769DOI: (10.1016/j.rbmo.2015.09.002) Copyright © 2015 Reproductive Healthcare Ltd. Terms and Conditions