ChepkwonyChatterjee: Difference between revisions
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Human vision science has been generally defined based on the presence of four types of photopigments in the retina: rods and three types of cones. Rods are responsible for peripheral vision under scotopic and mesopic lighting conditions. Rods are generally not associated with color vision. The cones on the other hand are present in the foveal region and are responsible for color vision. The L,M,S cones are sensitive to different wavelength ranges of light. | Human vision science has been generally defined based on the presence of four types of photopigments in the retina: rods and three types of cones. Rods are responsible for peripheral vision under scotopic and mesopic lighting conditions. Rods are generally not associated with color vision. The cones on the other hand are present in the foveal region and are responsible for color vision. The L,M,S cones are sensitive to different wavelength ranges of light. | ||
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There has been a recent discovery [http://www.jneurosci.org/content/20/2/600.full] of | There has been a recent discovery [http://www.jneurosci.org/content/20/2/600.full] of another type of non-rod non-cone photopigment in the human retina, and this is melanopsin present in the specialized ganglion cells of the retina. Melanopsin in the retina has been studied to the extent that its primary function has been determined to be signaling changes in ambient light levels to the brain throughout the day for unconscious visual reflexes, such as pupillary constriction, and regulating a number of daily behavioral and physiological rhythms, collectively called circadian rhythms. It has been suspected that Melanopsin may play some role in the human visual system as well. The role of melanopsin in color vision and temporally varying light intensity patterns is an emerging research area. | ||
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== MNI space == | == MNI space == | ||
Revision as of 21:13, 17 March 2012
LED Flicker system design
Background
Human vision science has been generally defined based on the presence of four types of photopigments in the retina: rods and three types of cones. Rods are responsible for peripheral vision under scotopic and mesopic lighting conditions. Rods are generally not associated with color vision. The cones on the other hand are present in the foveal region and are responsible for color vision. The L,M,S cones are sensitive to different wavelength ranges of light.
There has been a recent discovery [1] of another type of non-rod non-cone photopigment in the human retina, and this is melanopsin present in the specialized ganglion cells of the retina. Melanopsin in the retina has been studied to the extent that its primary function has been determined to be signaling changes in ambient light levels to the brain throughout the day for unconscious visual reflexes, such as pupillary constriction, and regulating a number of daily behavioral and physiological rhythms, collectively called circadian rhythms. It has been suspected that Melanopsin may play some role in the human visual system as well. The role of melanopsin in color vision and temporally varying light intensity patterns is an emerging research area.
MNI space
MNI is an abbreviation for Montreal Neurological Institute.
Methods
Measuring retinotopic maps
Retinotopic maps were obtained in 5 subjects using Population Receptive Field mapping methods Dumoulin and Wandell (2008). These data were collected for another research project in the Wandell lab. We re-analyzed the data for this project, as described below.
Subjects
Subjects were 5 healthy volunteers.
MR acquisition
Data were obtained on a GE scanner. Et cetera.
MR Analysis
The MR data was analyzed using mrVista software tools.
Pre-processing
All data were slice-time corrected, motion corrected, and repeated scans were averaged together to create a single average scan for each subject. Et cetera.
PRF model fits
PRF models were fit with a 2-gaussian model.
MNI space
After a pRF model was solved for each subject, the model was trasnformed into MNI template space. This was done by first aligning the high resolution t1-weighted anatomical scan from each subject to an MNI template. Since the pRF model was coregistered to the t1-anatomical scan, the same alignment matrix could then be applied to the pRF model.
Once each pRF model was aligned to MNI space, 4 model parameters - x, y, sigma, and r^2 - were averaged across each of the 6 subjects in each voxel.
Et cetera.
Results - What you found
Retinotopic models in native space
Some text. Some analysis. Some figures.
Retinotopic models in individual subjects transformed into MNI space
Some text. Some analysis. Some figures.
Retinotopic models in group-averaged data on the MNI template brain
Some text. Some analysis. Some figures. Maybe some equations.
Equations
If you want to use equations, you can use the same formats that are use on wikipedia.
See wikimedia help on formulas for help.
This example of equation use is copied and pasted from wikipedia's article on the DFT.
The sequence of N complex numbers x0, ..., xN−1 is transformed into the sequence of N complex numbers X0, ..., XN−1 by the DFT according to the formula:
where i is the imaginary unit and is a primitive N'th root of unity. (This expression can also be written in terms of a DFT matrix; when scaled appropriately it becomes a unitary matrix and the Xk can thus be viewed as coefficients of x in an orthonormal basis.)
The transform is sometimes denoted by the symbol , as in or or .
The inverse discrete Fourier transform (IDFT) is given by
Retinotopic models in group-averaged data projected back into native space
Some text. Some analysis. Some figures.
Conclusions
Here is where you say what your results mean.
References - Resources and related work
References
Software
Appendix I - Code and Data
Code
Data
Appendix II - Work partition (if a group project)
Brian and Bob gave the lectures. Jon mucked around on the wiki.