Changes for page 2. Example of use
Last modified by puchades on 2020/10/06 13:18
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... ... @@ -1,28 +1,19 @@ 1 1 == (% style="color:#c0392b" %)How can I identify brain regions in my images?(%%) == 2 2 3 3 (% class="wikigeneratedid" %) 4 -By using QuickNII, you will be able to register this image series to the mouse reference atlas version of your choice and obtain adapted atlas maps and coordinates. Further, in-plane non-linear adjustments can be made with VisuAlign in order to obtain a more precise registration. The regions shown in the example below are color coded and correspond to Mouse CCFv3_2017 atlas ^^1^^.4 +By using QuickNII, you will be able to register this image series to the mouse reference atlas version of your choice and obtain adapted atlas maps and coordinates. Further, in-plane non-linear adjustments can be made with VisuAlign in order to obtain a more precise registration. The regions shown in the example below are color coded and correspond to Mouse CCFv3_2017 atlas ( Oh et al. 2014). 5 5 6 6 (% class="wikigeneratedid" id="H" %) 7 7 (% style="color:#c0392b" %)[[image:Doublet_illust_NOP_tta.png]] 8 8 9 -Histological data available on EBRAINS: [[DOI 10.25493/AYBB-BXV>>https://kg.ebrains.eu/search/?facet_type[0]=Dataset&q=neuropsin#Dataset/d56b1fe14bb84987a3a2340e21652b2d]] 10 10 11 11 == (% style="color:#c0392b" %)How can I map the position of my reconstructed neuron?(%%) == 12 12 13 -After in-vivo electrophysiology experiments, the recorded neurons are filled with neurobiotin making them visible on histological images. These images are registered to the Mouse atlas CCFv3_2017 ^^1^^. The extracted coordinates of the neuron soma and the coordinates of the neuronal arbor, could then be mapped in the 3D reference space.12 +After in-vivo electrophysiology experiments, the recorded neurons are filled with neurobiotin making them visible on histological images. These images are registered to the Mouse atlas CCFv3_2017 ( Oh et al. 2014). The extracted coordinates of the neuron soma and the coordinates of the neuronal arbor, could then be mapped in the 3D reference space. 14 14 15 15 16 16 17 -(% style="text-align:center" %) 18 -[[image:QNII_neuron_recons.png||height="600" width="565"]] 19 19 20 -(% class="wikigeneratedid" %) 21 -Image from Bjerke et al. 2018. //Front. Neuroinform.// 12:82. [[doi:10.3389/fnana.2018.00082 >>https://www.frontiersin.org/articles/10.3389/fnana.2018.00082/full]] 22 - 23 -(% class="wikigeneratedid" %) 24 -Electrophysiological data available on EBRAINS: DOI: [[10.25493/ADRK-VJP>>https://kg.ebrains.eu/search/?facet_type[0]=Dataset&q=grillner#Dataset/749eab9b-3159-4eb8-a36b-85757208e3c1]] 25 - 26 26 == (% style="color:#c0392b" %)How can I count my labelled cells?(%%) == 27 27 28 28 ... ... @@ -33,7 +33,4 @@ 33 33 Image from Groeneboom NE, Yates SC, Puchades MA and Bjaalie JG (2020) Nutil: A Pre- and Post-processing Toolbox for Histological Rodent Brain Section Images. //Front. Neuroinform.// 14:37. doi: [[10.3389/fninf.2020.00037>>url:https://www.frontiersin.org/articles/10.3389/fninf.2020.00037/full]] 34 34 35 35 36 - 37 - 38 - 39 -~1. (Oh et al. 2014) 27 +== (% style="color:#c0392b" %)How can I map the position of my electrode?(%%) ==