Abstract
Objective
Brain atlases are important research tools enabling researchers to focus their investigations on specific anatomically defined brain regions and are used in many MRI applications, e.g. in fMRI, morphometry, whole brain spectroscopy, et cetera. Despite their extensive use and numerous versions they usually consist of predefined rigid brain regions with a given level of detail often degrading them to a non-ideal tool in special research topics.
Result
To overcome this intrinsic weakness we present a graphical user interface application which allows researchers to easily create mouse brain atlases with an adjustable user-defined level of detail and coverage to match specific research questions.
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Introduction
In many Magnetic Resonance Imaging (MRI) post-processing procedures brain atlases are used to investigate anatomically defined brain regions like e.g., in functional-MRI, morphometry, whole brain spectroscopy, et cetera. These brain atlases enable researchers to focus their investigations on specific brain areas by combining the voxel-based MR data from one or several brain regions of interest (ROI).
The main limitation of the currently available brain atlases standardly used in MR research (for instance WFU Pickatlas [1], AAL [2], Talairach [3], Dorr [4]) is their inflexibility due to an initial ROI pre-definition. The modification of pre-defined brain regions can be complicated and, thus, the level of detail is fixed. For instance, defining a sub-area within a ROI is usually only possible with considerable effort and requires expert knowledge.
An MRI atlas usually consists of two datasets: 1) an annotation image file which comprises integer numbers in a 3D space, representing the location of anatomically defined brain regions, and 2) a corresponding file (often a text file) which links the numbers of the annotation image with the name of the brain regions.
Material and method
We present a GUI (graphical user interface) application (written in MATLAB, The MathWorks, Inc., Natick, Massachusetts, United States) which allows researchers to easily create mouse brain atlases with an adjustable level of detail and coverage to match specific research questions.
Based on the Allen Mouse Common Coordinate Framework brain atlas [5] the user of our application can select and afterwards export ROIs in a newly created atlas. This procedure yields an image file (in nifty format;.nii) containing the annotation (anatomical) information together with a text file linking the integer numbers of the annotation image with the brain regions. These files can then be used like any other typical atlas-defining files.
The underlying data structure of the Allen Mouse brain atlas is initially given in big brain divisions (e.g., ‘Basic cell groups’, ‘fiber tracts’, etc.) as ‘parent’-regions whose children, grandchildren, great-grandchildren and so on are defining finer, and thus more specific, brain regions. Due to the high resolution of the Allen atlas (up to 10 µm; isotropic) ROIs can reach the level of single neuronal layers. As a compromise between data size and detail of ROIs, we chose the 50 µm variant.
Furthermore, for convenience the annotation image is additionally transformed into the Paxinos space by a SPM batch file, which could be replaced by experienced users (details described in the manual).
Transformation into the Paxinos space
To transform the Allen atlas data into the Paxinos space SPM’s ‘oldnormalize’ function was used with the anatomical/structural image from the Dorr atlas [4] as template, which was previously transformed into the Paxinos space [6, 7]. Since the provided average Nissl image of the Allen atlas was not suitable for a transformation with a satisfactory result (most probably due to different image modalities), we created a simulated anatomical image. To do so, we defined ROIs consisting solely of grey matter, white matter, and cerebrospinal fluid and assigned values to them mimicking the intensity distribution of the template, respectively (see Fig. 1 for results). The thus obtained transformation field is then applied to newly created atlases via an SPM batch file.
Result
In the application, the ROI hierarchical data structure is represented as a tree (Fig. 2, left) which grows with the respective levels of detail. To select ROIs the user right-clicks on a node in the tree (selected regions are in a green font) and the application combines the subjacent defined brain structure. For a coarse visual inspection, a 3D model of the selected ROIs can be presented (the ‘transparency’ slider sets the transparency of a selected ROI, see Fig. 2, right). After creating an atlas, it is immediately presented in the SPM [8] ‘Check Reg’ function, providing the possibility for a more detailed inspection (Fig. 3; with an additional example of the annotation text file).
Further functionalities of our application include:
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Exporting selected ROIs as binary mask files each representing the selected ROIs.
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Selecting the hemisphere: ROIs can be separated in both, or in the left and right hemisphere.
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Possibility to select ‘parental’ ROIs and additionally some of their sub-areas.
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For an easier integration of already established post-processing routines, the created atlas is automatically transformed into the Paxinos space.
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A ‘load’ function based on a.txt file to modify an already created atlas.
The atlas can be used as any other conventional atlas dataset in structural, functional analysis workflows, e.g., in SPM’s ‘imcalc’ routine using an expression like ‘i1.*(i2 = = XX)’ (where XX represents the ROI number), using a binary mask directly in FSL’s ‘fslmask’ routine, or even implement the atlas in other apps like the CONN toolbox (www.nitrc.org/projects/conn, RRID:SCR_009550) [9]. For further details the user is referred to the corresponding manuals of these tools. Furthermore, example scripts of ROI time course extraction are provided in the online repository.
Discussion
The presented application allows scientists to create mouse brain atlases with a level of detail matching their obtained data resolution and/or their specific research question. Due to its simplicity, flexibility, and adaptability we hope that it becomes a useful tool. The application can be downloaded here: https://github.com/DrCarbonCIMH/MouseAtlas.
It should be noted that, as with any other tools, it is the user’s responsibility to take care about the correctness and accuracy of the created data, especially regarding ROI definition and space transformation.
Furthermore, we will explore the possibility to extend the application by other datasets such as developing mouse, rat, or human brain atlases.
References
Maldjian JA, Laurienti PJ, Kraft RA, Burdette JH (2003) An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage 19(3):1233–1239
Rolls ET, Joliot M, Tzourio-Mazoyer N (2015) Implementation of a new parcellation of the orbitofrontal cortex in the automated anatomical labeling atlas. Neuroimage 122:1–5
Talairach J, Tournoux P (1988) Co-planar stereotaxic atlas of the human brain. In: 3-Dimensional proportional system: an approach to cerebral imaging ISBN: 9780865772939
Dorr AE, Lerch JP, Spring S, Kabani N, Henkelman RM (2008) High resolution three-dimensional brain atlas using an average magnetic resonance image of 40 adult C57Bl/6J mice. Neuroimage 42(1):60–69
Lein ES, Hawrylycz MJ, Ao N, Ayres M, Bensinger A, Bernard A, Boe AF, Boguski MS, Brockway KS, Byrnes EJ, Chen L, Chen L, Chen T-M, Chi Chin M, Chong J, Crook BE, Czaplinska A, Dang CN, Datta S, Dee NR, Desaki AL, Desta T, Diep E, Dolbeare TA, Donelan MJ, Dong H-W, Dougherty JG, Duncan BJ, Ebbert AJ, Eichele G, Estin LK, Faber C, Facer BA, Fields R, Fischer SR, Fliss TP, Frensley C, Gates SN, Glattfelder KJ, Halverson KR, Hart MR, Hohmann JG, Howell MP, Jeung DP, Johnson RA, Karr PT, Kawal R, Kidney JM, Knapik RH, Kuan CL, Lake JH, Laramee AR, Larsen KD, Lau C, Lemon TA, Liang AJ, Liu Y, Luong LT, Michaels J, Morgan JJ, Morgan RJ, Mortrud MT, Mosqueda NF, Ng LL, Ng R, Orta GJ, Overly CC, Pak TH, Parry SE, Pathak SD, Pearson OC, Puchalski RB, Riley ZL, Rockett HR, Rowland SA, Royall JJ, Ruiz MJ, Sarno NR, Schaffnit K, Shapovalova NV, Sivisay T, Slaughterbeck CR, Smith SC, Smith KA, Smith BI, Sodt AJ, Stewart NN, Stumpf K-R, Sunkin SM, Sutram M, Tam A, Teemer CD, Thaller C, Thompson CL, Varnam LR, Visel A, Whitlock RM, Wohnoutka PE, Wolkey CK, Wong VY, Wood M, Yaylaoglu MB, Young RC, Youngstrom BL, Feng Yuan X, Zhang B, Zwingman TA, Jones AR (2006) Genome-wide atlas of gene expression in the adult mouse brain. Nature 445:168
Gass N, Weber-Fahr W, Sartorius A, Becker R, Didriksen M, Stensbol TB, Bastlund JF, Meyer-Lindenberg A, Schwarz AJ (2016) An acetylcholine alpha7 positive allosteric modulator rescues a schizophrenia-associated brain endophenotype in the 15q13.3 microdeletion, encompassing CHRNA7. Eur Neuropsychopharmacol 26(7):1150–1160
Paxinos G (2013) Paxinos and Franklin's the mouse brain in stereotaxic coordinates. Academic Press, USA
Penny WD, Friston KJ, Ashburner JT, Kiebel SJ, Nichols TE (2011) Statistical parametric mapping: the analysis of functional brain images. Academic press, USA
Whitfield-Gabrieli S, Nieto-Castanon A (2012) Conn: a functional connectivity toolbox for correlated and anticorrelated brain networks. Brain Connect 2(3):125–141
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MS, LZ, NG and WW-F contributed conception and development of this work; MS and LZ prepared data processing and substantial functionality; NG and WW-F validated data output; All authors contributed application design, test, and handling; All authors contributed to manuscript revision, read, and approved the submitted version.
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All experiments leading to the data used had been performed according to the regulations covering animal experimentation within the European Union (European Communities Council Directive 86/609/EEC) and within the German Animal Welfare Act, and were approved by the German animal welfare authorities (Regierungspräsidium Karlsruhe).
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Sack, M., Zheng, L., Gass, N. et al. Interactive tool to create adjustable anatomical atlases for mouse brain imaging. Magn Reson Mater Phy 34, 183–187 (2021). https://doi.org/10.1007/s10334-020-00866-0
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DOI: https://doi.org/10.1007/s10334-020-00866-0