Embryo at 16 hpf*
Embryo at 20 hpf
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* hours post fertilization
Live Embryo imaged with Light Sheet Microscopy: Nuclei, Membrane
In-situ Specimen at 16 hpf imaged with Confocal Microscopy: Nuclei, Pax3/7
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Feature - based
Intensity - based
(Source: MathWorks)
Mette Handberg-Thorsager
Mette Handberg-Thorsager
The number of cell nuclei is used as a measure for staging the in-situ specimen
Number of cell nuclei in in-situ specimens at 16 and 20 hpf
Selection of the correct time point is based on maximum bi-partite matching
Feature Detection with Automatic Scale Selection, Lindeberg, T., International Journal of Computer Vision, 1998
Live Embryo: Nuclei. Cell nuclei positions were fitted to an ellipsoid
In-situ Specimen: Nuclei. Cell nuclei positions were fitted to an ellipsoid
Choosing a few corresponding nuclei helps estimate the underlying transform
Live Embryo: Nuclei, Membrane
In-situ Specimen: Nuclei
Maximum Bi-partite Matching helps fine-tune the transform
Live Embryo: Nuclei
In-situ Specimen AFTER transformation: Nuclei
In-situ Specimen BEFORE transformation: Nuclei
Live Embryo: Nuclei
In-situ Specimen imaged with Confocal Microscopy: Nuclei, pax3/7
In-situ Specimen imaged with Confocal Microscopy: Nuclei, pax6
Co-expression (Max z-projection ), obtained using ProSPr *
* Whole-organism cellular gene expression atlas, Vergara et al, PNAS June 6, 2017 114 (23) 5878-5885
Future: By-passing the hand-picking of corresponding nuclei
Future: Adding Single Cell RNA-Sequencing data to the mix
Developmental Cell Lineage
Mette Handberg-Thorsager
Mette Handberg-Thorsager
Bruno Vellutini
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