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Advances in multifocal methods for imaging human brain activity

机译:多焦点方法对人脑活动进行成像的研究进展

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The typical multifocal stimulus used in visual evoked potential (VEP) studies consists of about 60 checkerboard stimulus patches each independently contrast reversed according to an m-sequence. Cross correlation of the response (EEG, MEG, ERG, or fMRI) with the m-sequence results in a series of response kernels for each response channel and each stimulus patch. In the past the number and complexity of stimulus patches has been constrained by graphics hardware, namely the use of look-up-table (LUT) animation methods. To avoid such limitations we replaced the LUTs with true color graphic sprites to present arbitrary spatial patterns. To demonstrate the utility of the method we have recorded simultaneously from 192 cortically scaled stimulus patches each of which activate about 12mm~2 of cortex in area V1. Because of the sparseness of cortical folding, very small stimulus patches and robust estimation of dipole source orientation, the method opens a new window on precise spatio-temporal mapping of early visual areas. The use of sprites also enables multiplexing stimuli such that at each patch location multiple stimuli can be presented. We have presented patterns with different orientations (or spatial frequencies) at the same patch locations but independently temporally modulated, effectively doubling the number of stimulus patches, to explore cell population interactions at the same cortical locus. We have also measured nonlinear responses to adjacent pairs of patches, thereby getting an edge response that doubles the spatial sampling density to about 1.8 mm on cortex.
机译:视觉诱发电位(VEP)研究中使用的典型多焦点刺激物由大约60个棋盘刺激斑块组成,每个斑块刺激块根据m序列独立地反转。响应(EEG,MEG,ERG或fMRI)与m序列的互相关会为每个响应通道和每个刺激斑块生成一系列响应内核。在过去,刺激补丁的数量和复杂性一直受到图形硬件的限制,即使用查找表(LUT)动画方法。为了避免此类限制,我们用真彩色图形精灵替换了LUT,以呈现任意的空间图案。为了证明该方法的实用性,我们同时记录了192个皮质缩放的刺激斑块,每个斑块都激活了V1区域约12mm〜2的皮质。由于皮质折叠的稀疏性,很小的刺激斑块和偶极子源方位的可靠估计,该方法为早期视觉区域的精确时空映射开辟了新窗口。子画面的使用还使得能够复用刺激,从而可以在每个贴片位置呈现多个刺激。我们已经提出了在相同贴片位置具有不同方向(或空间频率)但独立地进行时间调制的模式,有效地使刺激贴片的数量增加了一倍,以探索相同皮质位点上的细胞群体相互作用。我们还测量了对相邻补丁对的非线性响应,从而获得了边缘响应,该响应使皮质上的空间采样密度加倍,达到约1.8 mm。

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