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Consider a set of classes and an uncertain input. Suppose, we do not have access to data and only have knowledge of perfect experts between a few classes in the set. What constitutes a consistent set of opinions? How can we use this to predict the opinions of experts on missing sub-domains? In this paper, we define a framework to analyze this problem. In particular, we define an expert graph where vertices represent classes and edges represent binary experts on the topics of their vertices. We derive necessary conditions for an expert graph to be valid. Further, we show that these conditions are also sufficient if the graph is a cycle, which can yield unintuitive results. Using these conditions, we provide an algorithm to obtain upper and lower bounds on the weights of unknown edges in an expert graph.

Deep neural networks (DNNs) typically have many weights. When errors appear in their weights, which are usually stored in non-volatile memories, their performance can degrade significantly. We review two recently presented approaches that improve the robustness of DNNs in complementary ways. In the first approach, we use error-correcting codes as external redundancy to protect the weights from errors. A deep reinforcement learning algorithm is used to optimize the redundancy-performance tradeoff. In the second approach, internal redundancy is added to neurons via coding. It enables neurons to perform robust inference in noisy environments.

Data is one of the most important assets of the information age, and its societal impact is undisputed. Yet, rigorous methods of assessing the quality of data are lacking. In this paper, we propose a formal definition for the quality of a given dataset. We assess a dataset’s quality by a quantity we call the expected diameter, which measures the expected disagreement between two randomly chosen hypotheses that explain it, and has recently found applications in active learning. We focus on Boolean hyperplanes, and utilize a collection of Fourier analytic, algebraic, and probabilistic methods to come up with theoretical guarantees and practical solutions for the computation of the expected diameter. We also study the behaviour of the expected diameter on algebraically structured datasets, conduct experiments that validate this notion of quality, and demonstrate the feasibility of our techniques.

Deep Neural Networks (DNNs) are a revolutionary force in the ongoing information revolution, and yet their intrinsic properties remain a mystery. In particular, it is widely known that DNNs are highly sensitive to noise, whether adversarial or random. This poses a fundamental challenge for hardware implementations of DNNs, and for their deployment in critical applications such as autonomous driving.In this paper we construct robust DNNs via error correcting codes. By our approach, either the data or internal layers of the DNN are coded with error correcting codes, and successful computation under noise is guaranteed. Since DNNs can be seen as a layered concatenation of classification tasks, our research begins with the core task of classifying noisy coded inputs, and progresses towards robust DNNs.We focus on binary data and linear codes. Our main result is that the prevalent parity code can guarantee robustness for a large family of DNNs, which includes the recently popularized binarized neural networks. Further, we show that the coded classification problem has a deep connection to Fourier analysis of Boolean functions.In contrast to existing solutions in the literature, our results do not rely on altering the training process of the DNN, and provide mathematically rigorous guarantees rather than experimental evidence.

Erwin Chargaff in 1950 made an experimental observation that the count of A is equal to the count of T and the count of C is equal to the count of G in DNA. This observation played a crucial role in the discovery of the double stranded helix structure by Watson and Crick. However, this symmetry was also observed in single stranded DNA. This phenomenon was termed as the 2nd Chargaff Rule. This symmetry has been verified experimentally in genomes of several different species not only for mononucleotides but also for reverse complement pairs of larger lengths upto a small error. While the symmetry in double stranded DNA is related to base pairing and replication mechanisms, the symmetry in a single stranded DNA is still a mystery in its function and source. In this work, we define a sequence generation model based on reverse complement tandem duplications. We show that this model generates sequences that satisfy the 2nd Chargaff Rule even when the duplication lengths are very small when compared to the length of sequences. We also provide estimates on the number of generations that are needed by this model to generate sequences that satisfy the 2nd Chargaff Rule. We provide theoretical bounds on the disruption in symmetry for different values of duplication lengths under this model. Moreover, we experimentally compare the disruption in the symmetry incurred by our model with what is observed in human genome data.

Duplication mutations play a critical role in the generation of biological sequences. Simultaneously, they have a deleterious effect on data stored using in-vivo DNA data storage. While duplications have been studied both as a sequence-generation mechanism and in the context of error correction, for simplicity these studies have not taken into account the presence of other types of mutations. In this work, we consider the capacity of duplication mutations in the presence of point-mutation noise, and so quantify the generation power of these mutations. We show that if the number of point mutations is vanishingly small compared to the number of duplication mutations of a constant length, the generation capacity of these mutations is zero. However, if the number of point mutations increases to a constant fraction of the number of duplications, then the capacity is nonzero. Lower and upper bounds for this capacity are also presented. Another problem that we study is concerned with the mismatch between code design and channel in data storage in the DNA of living organisms with respect to duplication mutations. In this context, we consider the uncertainty of such a mismatched coding scheme measured as the maximum number of input codewords that can lead to the same output.

The ability to store data in the DNA of a living organism has applications in a variety of areas including synthetic biology and watermarking of patented genetically-modified organisms. Data stored in this medium is subject to errors arising from various mutations, such as point mutations, indels, and tandem duplication, which need to be corrected to maintain data integrity. In this paper, we provide error-correcting codes for errors caused by tandem duplications, which create a copy of a block of the sequence and insert it in a tandem manner, i.e., next to the original. In particular, we present a family of codes for correcting errors due to tandem-duplications of a fixed length and any number of errors. We also study codes for correcting tandem duplications of length up to a given constant k, where we are primarily focused on the cases of k = 2, 3.

The majority of the human genome consists of repeated sequences. An important type of repeats common in the human genome are tandem repeats, where identical copies appear next to each other. For example, in the sequence AGTCTGTGC,TGTG is a tandem repeat, namely, generated from AGTCTGC by a tandem duplication of length 2. In this work, we investigate the possibility of generating a large number of sequences from a small initial string (called the seed) by tandem duplications of bounded length. Our results include exact capacity values for certain tandem duplication string systems with alphabet sizes 2, 3, and 4. In addition, motivated by the role of DNA sequences in expressing proteins via RNA and the genetic code, we define the notion of the expressiveness of a tandem duplication system, as the feasibility of expressing arbitrary substrings. We then completely characterize the expressiveness of tandem duplication systems for general alphabet sizes and duplication lengths. Noticing that a system with capacity = 1 is expressive, we prove that for an alphabet size ≥ 4, the capacity is strictly smaller than 1, independent of the seed and the duplication lengths. The proof of this limit on the capacity (note that the genomic alphabet size is 4), is related to an interesting result by Axel Thue from 1906 which states that there exist arbitrary length sequences with no tandem repeats (square-free) for alphabet size ≥ 3. Finally, our results illustrate that duplication lengths play a more significant role than the seed in generating a large number of sequences for these systems.