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. 2017;34:E005. doi: 10.1017/S0952523817000025

Imaging the adult zebrafish cone mosaic using optical coherence tomography—CORRIGENDUM

ALISON L HUCKENPAHLER, MELISSA A WILK, ROBERT F COOPER, FRANCIE MOEHRING, BRIAN A LINK, JOSEPH CARROLL, ROSS F COLLERY
PMCID: PMC8054337  PMID: 28965523

doi: https://doi.org/10.1017/S0952523816000092. Published by Cambridge University Press, 17 October, 2016.

When originally published, the article by the author included the wrong information in Figure 2, panel 2B as shown on page 3. The measurement was incorrectly listed as 257µm instead of 238µm.

The authors apologize for this error.

The corrected version of Figure 2, together with the full caption are shown below.

Fig. 2.

Fig. 2.

Deriving the lateral scale of in vivo OCT images of the fli1:eGFP zebrafish retina. (A) En face image generated by positioning the custom contour within the RNFL. Measurements (in pixels) were taken between multiple blood vessel branch points (white dots). (B) Corresponding ex vivo fluorescent microscopy image of the same retina, with measurements (in µm) taken between the same blood vessel branch points in (A). The OCT:microscopy measurements were averaged for each eye and used to determine the size of the OCT scan in µm. A scaling coefficient for each scan was calculated as the ratio between the measured size of the OCT scan to the nominal OCT scan size (in this case, 1200 µm). (C) The scaling coefficient for each scan was plotted against the axial length for that eye and fit with a linear model. Error bars represent one standard deviation for each eye.

Reference

  1. Huckenpahler A.L., Wilk M.A., Cooper R.F., Moehring F., Link B.A., Carroll J., & Collery R.F. (2016). Imaging the adult zebrafish cone mosaic using optical coherence tomography. Visual Neuroscience, 33, E011, 1 -7. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Visual Neuroscience are provided here courtesy of Cambridge University Press

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