Correction of depth intensity attenuation in confocal images of drosophila embryos

Manuel G. Forero; J. Pennack; A. R. Learte; A. Hidalgo

Correction of depth intensity attenuation in confocal images of drosophila embryos

Manuel G. Forero, J. Pennack, A. R. Learte, A. Hidalgo

Resultado de la investigación: Contribución a una conferencia › Artículo

Resumen

Idioma original	Inglés estadounidense
Páginas	397-400
Número de páginas	356
Estado	Publicada - 1 dic 2006
Publicado de forma externa	Sí
Evento	AIP Conference Proceedings - Duración: 1 dic 2006 → …

Conferencia

Conferencia	AIP Conference Proceedings
Período	1/12/06 → …

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Forero, M. G., Pennack, J., Learte, A. R., & Hidalgo, A. (2006). Correction of depth intensity attenuation in confocal images of drosophila embryos. 397-400. Papel presentado en AIP Conference Proceedings, .

@conference{73e64216ecd54f29ae5b36a0b32f026a,

title = "Correction of depth intensity attenuation in confocal images of drosophila embryos",

abstract = "It is common in confocal microscopy that, despite careful selection of embedding media, objectives etc., signal intensity drops with increasing focus depth (e.g in thick tissue samples). 3D confocal images suffer from intensity and contrast attenuation with depth. This problem causes difficulties in the analysis and visualisation of biological samples. We present a very simple and straightforward procedure to solve this problem in images where the objects of interest are embedded in deeper tissue layers. Here, we analyze cells stained in the deeper layers of the nervous system of Drosophila embryos. {\textcopyright} 2006 American Institute of Physics.",

author = "Forero, {Manuel G.} and J. Pennack and Learte, {A. R.} and A. Hidalgo",

year = "2006",

month = dec,

day = "1",

language = "American English",

pages = "397--400",

note = "AIP Conference Proceedings ; Conference date: 01-12-2006",

}

TY - CONF

T1 - Correction of depth intensity attenuation in confocal images of drosophila embryos

AU - Forero, Manuel G.

AU - Pennack, J.

AU - Learte, A. R.

AU - Hidalgo, A.

PY - 2006/12/1

Y1 - 2006/12/1

N2 - It is common in confocal microscopy that, despite careful selection of embedding media, objectives etc., signal intensity drops with increasing focus depth (e.g in thick tissue samples). 3D confocal images suffer from intensity and contrast attenuation with depth. This problem causes difficulties in the analysis and visualisation of biological samples. We present a very simple and straightforward procedure to solve this problem in images where the objects of interest are embedded in deeper tissue layers. Here, we analyze cells stained in the deeper layers of the nervous system of Drosophila embryos. © 2006 American Institute of Physics.

AB - It is common in confocal microscopy that, despite careful selection of embedding media, objectives etc., signal intensity drops with increasing focus depth (e.g in thick tissue samples). 3D confocal images suffer from intensity and contrast attenuation with depth. This problem causes difficulties in the analysis and visualisation of biological samples. We present a very simple and straightforward procedure to solve this problem in images where the objects of interest are embedded in deeper tissue layers. Here, we analyze cells stained in the deeper layers of the nervous system of Drosophila embryos. © 2006 American Institute of Physics.

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M3 - Paper

SP - 397

EP - 400

T2 - AIP Conference Proceedings

Y2 - 1 December 2006

ER -