Supplemental data to accompany a manuscript in preparation presently entitled:
Combining genome-scale Drosophila 3D neuroanatomical data by bridging template brains. James D. Manton, Aaron D. Ostrovsky, Lea Goetz, Marta Costa, Torsten Rohlfing, Gregory S.X.E. Jefferis
biorxiv preprint available at doi: 10.1101/006353
Template | URL |
---|---|
IS2 | http://dx.doi.org/10.5281/zenodo.10595 |
JFRC2 | http://dx.doi.org/10.5281/zenodo.10567 |
FCWB | http://dx.doi.org/10.5281/zenodo.10568 |
T1 | http://dx.doi.org/10.5281/zenodo.10590 |
IBNWB | http://dx.doi.org/10.5281/zenodo.10569 |
Cell07 | http://dx.doi.org/10.5281/zenodo.10570 |
D. Melanogaster | http://dx.doi.org/10.5281/zenodo.10591 |
D. Simulans | http://dx.doi.org/10.5281/zenodo.10594 |
D. Virilis | http://dx.doi.org/10.5281/zenodo.10593 |
Please ensure that you cite the original authors when making use of the following data in any publication. We would also request that you cite the VFB project (see here). The registrations for the Janelia FlyLight data, along with the mirroring registrations and bridging registrations used in the processing of the Ito and Cachero & Ostrovsky datasets were generated by members of the Jefferis group. Please contact us, using the contact information in the preprint, for citation info if you wish to use the data in a paper.
We found that the presence of the lamina in the original images decreased the registration success rate, although for the vast majority (3436 out of 3501) the central brain still registered well. The list of images with good overall registration (goodimages) is here. The list of images with good central brain registration (goodbrains) is here. Following registration, the reformatted images were quantised to 8 bit.
The registered data are available here.
The original data was described in this paper (Jenett et al., 2012, Cell Rep. 2(4): 991--1001).
We used a flipping registration based on a spatially calibrated version of the JFRC/VFB template brain (JFRC2) to take data from the fly's right to the fly's left, which is where the original data lives. Specifically, we used this JFRC2 mirror registration and this JFRC2 flipping registration as described in the readme here.
The registered data are available here.
The original data was described in this paper (Ito et al., 2013, Curr. Biol. 23(8): 644--655).
We used a specific crop (vertical offset of 94 pixels) of the registered stacks supplied by Tzumin Lee in order to correct an offset difference and result in stacks in the same space as the JFRC2 template brain.
The registered data are available here.
The original data was described in this paper (Yu et al., 2013, Curr. Biol. 23(8): 633-43).
JFRC2 registered images of the fruitless neuroblast clones are provided here.
Both male and female versions are provided regardless of whether a sexual dimorphism was observed. The data were cross-registered against the JFRC2 template by applying JFRC2_IS2 bridging registration. The original data (registered against IS2 template) are available here.
The original data was described in this paper (Cachero et al., 2010, Curr. Biol. 20(18): 1589--1601).
The transformations between different reference spaces described in the paper use the CMTK registration suite. For convenience this functionality has been wrapped in an R package, nat.templatebrains, which allows users to make transformations by naming template brain objects. For greater convenience some of these registrations are available in a single R package nat.flybrains, which allows objects to be transformed with a single line of code having R itself and CMTK as the sole external dependencies.