Data-robust tight lower bounds to the information carried by spike times of a neuronal population.

We develop new data-robust lower-bound methods to quantify the information carried by the timing of spikes emitted by neuronal populations. These methods have better sampling properties and are tighter than previous bounds based on neglecting correlation in the noise entropy. Our new lower bounds are precise also in the presence of strongly correlated firing. They are not precise only if correlations are strongly stimulus modulated over a long time range. Under conditions typical of many neurophysiological experiments, these techniques permit precise information estimates to be made even with data samples that are three orders of magnitude smaller than the size of the response space.

An exact method to quantify the information transmitted by different mechanisms of correlational coding.

We derive a new method to quantify the impact of correlated firing on the information transmitted by neuronal populations. This new method considers, in an exact way, the effects of high order spike train statistics, with no approximation involved, and it generalizes our previous work that was valid for short time windows and small populations. The new technique permits one to quantify the information transmitted if each cell were to convey fully independent information separately from the information available in the presence of synergy-redundancy effects. Synergy-redundancy effects are shown to arise from three possible contributions: a redundant contribution due to similarities in the mean response profiles of different cells; a synergistic stimulus-dependent correlational contribution quantifying the information content of changes of correlations with stimulus, and a stimulus-independent correlational contribution term that reflects interactions between the distribution of rates of individual cells and the average level of cross-correlation. We apply the new method to simultaneously recorded data from somatosensory and visual cortices. We demonstrate that it constitutes a reliable tool to determine the role of cross-correlated activity in stimulus coding even when high firing rate data (such as multi-unit recordings) are considered.