Virtual Karyotyping Reveals Greater Chromosomal Stability in Neural Cells Derived by Transdifferentiation than Those from Stem Cells  Uri Weissbein, Uri.

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Virtual Karyotyping Reveals Greater Chromosomal Stability in Neural Cells Derived by Transdifferentiation than Those from Stem Cells  Uri Weissbein, Uri Ben-David, Nissim Benvenisty  Cell Stem Cell  Volume 15, Issue 6, Pages 687-691 (December 2014) DOI: 10.1016/j.stem.2014.10.018 Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 1 Chromosomal Aberrations in Mouse Neural Cells Either Differentiated from Pluripotent and Adult Stem Cells or Transdifferentiated (A) Schematic representation of the differentiation pathways into neural cells. (B) E-karyotyping analysis of neural cells differentiated from different sources. Shown are moving average plots of representative examples for genomic aberrations in neural cells. A gray background represents aneuploidy as recognized by the PCF algorithm. (C) Distribution of the studies according to the samples’ source and genomic status. Each sector is labeled with the percentage of studies out of the total number of studies, and the absolute number of studies is mentioned within brackets. (D) Ideograms representing the chromosomal aberrations identified in mouse neural cells. Chromosomal aberrations in samples from similar cells from the same study are interconnected by a line. Bars to the right of the chromosomes represent gains and bars to the left represent deletions. Cell Stem Cell 2014 15, 687-691DOI: (10.1016/j.stem.2014.10.018) Copyright © 2014 Elsevier Inc. Terms and Conditions

Figure 2 Chromosomal Abnormalities in Human Neural Cells Either Differentiated from Pluripotent and Adult Stem Cells or Transdifferentiated (A) E-karyotyping analysis of human neural cells. Shown are moving average plots of representative examples for chromosomal aneuploidies in neural cells derived from different sources. A gray background represents aneuploidy as recognized by the PCF algorithm. (B) Distribution of the studies according to the samples’ source and genomic status. Each sector is labeled with the percentage of studies out of the total number of studies, and the absolute number of studies is mentioned within brackets. (C) Ideograms representing the chromosomal aberrations identified in human neural cells. Chromosomal aberrations in samples from similar cells from the same study are interconnected by a line. Bars to the right of the chromosomes represent chromosome gain, and bars to the left represent chromosome loss. (D) Bar plot of the percentage of aberrant samples from each source of neural cells. The transdifferentiation samples are divided by the type of the reprogramming factors used. NF, neural factors; NF+PF, neural factors together with pluripotency factors. Cell Stem Cell 2014 15, 687-691DOI: (10.1016/j.stem.2014.10.018) Copyright © 2014 Elsevier Inc. Terms and Conditions