Capacity of a Class of Deterministic Relay Channels

The capacity of a class of deterministic relay channels with the transmitter input X, the receiver output Y, the relay output Y_1 = f(X, Y), and a separate communication link from the relay to the receiver with capacity R_0, is shown to be C(R_0) = \max_{p(x)} \min \{I(X;Y)+R_0, I(X;Y, Y_1) \}. Thus every bit from the relay is worth exactly one bit to the receiver. Two alternative coding schemes are presented that achieve this capacity. The first scheme, ``hash-and-forward'', is based on a simple yet novel use of random binning on the space of relay outputs, while the second scheme uses the usual ``compress-and-forward''. In fact, these two schemes can be combined together to give a class of optimal coding schemes. As a corollary, this relay capacity result confirms a conjecture by Ahlswede and Han on the capacity of a channel with rate-limited state information at the decoder in the special case when the channel state is recoverable from the channel input and the output.Comment: 17 pages, submitted to IEEE Transactions on Information Theor

A bijection between unicellular and bicellular maps

In this paper we present a combinatorial proof of a relation between the generating functions of unicellular and bicellular maps. This relation is a consequence of the Schwinger-Dyson equation of matrix theory. Alternatively it can be proved using representation theory of the symmetric group. Here we give a bijective proof by rewiring unicellular maps of topological genus $(g+1)$ into bicellular maps of genus $g$ and pairs of unicellular maps of lower topological genera. Our result has immediate consequences for the folding of RNA interaction structures, since the time complexity of folding the transformed structure is $O((n+m)^5)$, where $n,m$ are the lengths of the respective backbones, while the folding of the original structure has $O(n^6)$ time complexity, where $n$ is the length of the longer sequence.Comment: 18 pages, 13 figure