Changes for page 2. Example of use
Last modified by puchades on 2020/10/06 13:18
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... ... @@ -1,20 +1,28 @@ 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 (Oh et al.2014).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^^ . 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]] 9 9 10 10 == (% style="color:#c0392b" %)How can I map the position of my reconstructed neuron?(%%) == 11 11 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.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. 13 13 14 14 15 15 17 +(% style="text-align:center" %) 16 16 [[image:QNII_neuron_recons.png||height="600" width="565"]] 17 17 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 + 18 18 == (% style="color:#c0392b" %)How can I count my labelled cells?(%%) == 19 19 20 20 ... ... @@ -26,3 +26,8 @@ 26 26 27 27 28 28 == (% style="color:#c0392b" %)How can I map the position of my electrode?(%%) == 37 + 38 + 39 + 40 + 41 +~1. (Oh et al. 2014)