Paper
10 March 2015 Quantitative analyses for elucidating mechanisms of cell fate commitment in the mouse blastocyst
Néstor Saiz, Minjung Kang, Alberto Puliafito, Nadine Schrode, Panagiotis Xenopoulos, Xinghua Lou, Stefano Di Talia, Anna-Katerina Hadjantonakis
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Abstract
In recent years we have witnessed a shift from qualitative image analysis towards higher resolution, quantitative analyses of imaging data in developmental biology. This shift has been fueled by technological advances in both imaging and analysis software. We have recently developed a tool for accurate, semi-automated nuclear segmentation of imaging data from early mouse embryos and embryonic stem cells. We have applied this software to the study of the first lineage decisions that take place during mouse development and established analysis pipelines for both static and time-lapse imaging experiments. In this paper we summarize the conclusions from these studies to illustrate how quantitative, single-cell level analysis of imaging data can unveil biological processes that cannot be revealed by traditional qualitative studies.
© (2015) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Néstor Saiz, Minjung Kang, Alberto Puliafito, Nadine Schrode, Panagiotis Xenopoulos, Xinghua Lou, Stefano Di Talia, and Anna-Katerina Hadjantonakis "Quantitative analyses for elucidating mechanisms of cell fate commitment in the mouse blastocyst", Proc. SPIE 9334, Optical Methods in Developmental Biology III, 93340D (10 March 2015); https://doi.org/10.1117/12.2081232
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KEYWORDS
Image segmentation

Proteins

Biological research

Quantitative analysis

Image processing

Biology

Image analysis

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