Searcharxiv⌕ Search

arXiv subjects

Pierre Baldi

Publications and source records attributed to Pierre Baldi.

93 records · Page 6Linked to original sources

Complex-Valued Autoencoders

Autoencoders are unsupervised machine learning circuits whose learning goal is to minimize a distortion measure between inputs and outputs. Linear autoencoders can be defined over any field and only real-valued linear autoencoder have been studied so far. Here we study complex-valued linear autoencoders where the components of the training vectors and adjustable matrices are defined over the complex field with the $L_2$ norm. We provide simpler and more general proofs that unify the real-valued and complex-valued cases, showing that in both cases the landscape of the error function is invariant under certain groups of transformations. The landscape has no local minima, a family of global minima associated with Principal Component Analysis, and many families of saddle points associated with orthogonal projections onto sub-space spanned by sub-optimal subsets of eigenvectors of the covariance matrix. The theory yields several iterative, convergent, learning algorithms, a clear understanding of the generalization properties of the trained autoencoders, and can equally be applied to the hetero-associative case when external targets are provided. Partial results on deep architecture as well as the differential geometry of autoencoders are also presented. The general framework described here is useful to classify autoencoders and identify general common properties that ought to be investigated for each class, illuminating some of the connections between information theory, unsupervised learning, clustering, Hebbian learning, and autoencoders.

cs.NE↗

Countering Gattaca: Efficient and Secure Testing of Fully-Sequenced Human Genomes (Full Version)

Recent advances in DNA sequencing technologies have put ubiquitous availability of fully sequenced human genomes within reach. It is no longer hard to imagine the day when everyone will have the means to obtain and store one's own DNA sequence. Widespread and affordable availability of fully sequenced genomes immediately opens up important opportunities in a number of health-related fields. In particular, common genomic applications and tests performed in vitro today will soon be conducted computationally, using digitized genomes. New applications will be developed as genome-enabled medicine becomes increasingly preventive and personalized. However, this progress also prompts significant privacy challenges associated with potential loss, theft, or misuse of genomic data. In this paper, we begin to address genomic privacy by focusing on three important applications: Paternity Tests, Personalized Medicine, and Genetic Compatibility Tests. After carefully analyzing these applications and their privacy requirements, we propose a set of efficient techniques based on private set operations. This allows us to implement in in silico some operations that are currently performed via in vitro methods, in a secure fashion. Experimental results demonstrate that proposed techniques are both feasible and practical today.

cs.CR↗

Privacy-Enhanced Methods for Comparing Compressed DNA Sequences

In this paper, we study methods for improving the efficiency and privacy of compressed DNA sequence comparison computations, under various querying scenarios. For instance, one scenario involves a querier, Bob, who wants to test if his DNA string, $Q$, is close to a DNA string, $Y$, owned by a data owner, Alice, but Bob does not want to reveal $Q$ to Alice and Alice is willing to reveal $Y$ to Bob \emph{only if} it is close to $Q$. We describe a privacy-enhanced method for comparing two compressed DNA sequences, which can be used to achieve the goals of such a scenario. Our method involves a reduction to set differencing, and we describe a privacy-enhanced protocol for set differencing that achieves absolute privacy for Bob (in the information theoretic sense), and a quantifiable degree of privacy protection for Alice. One of the important features of our protocols, which makes them ideally suited to privacy-enhanced DNA sequence comparison problems, is that the communication complexity of our solutions is proportional to a threshold that bounds the cardinality of the set differences that are of interest, rather than the cardinality of the sets involved (which correlates to the length of the DNA sequences). Moreover, in our protocols, the querier, Bob, can easily compute the set difference only if its cardinality is close to or below a specified threshold.

cs.CR↗