arXiv subjects

Olgica Milenkovic

Publications and source records attributed to Olgica Milenkovic.

At least 109 records · Page 6Linked to original sources

arXiv2016

Weakly Mutually Uncorrelated Codes

We introduce the notion of weakly mutually uncorrelated (WMU) sequences, motivated by applications in DNA-based storage systems and synchronization protocols. WMU sequences are characterized by the property that no sufficiently long suffix of one sequence is the prefix of the same or another sequence. In addition, WMU sequences used in DNA-based storage systems are required to have balanced compositions of symbols and to be at large mutual Hamming distance from each other. We present a number of constructions for balanced, error-correcting WMU codes using Dyck paths, Knuth's balancing principle, prefix synchronized and cyclic codes.

cs.IT↗

arXiv2016

Balanced Permutation Codes

Motivated by charge balancing constraints for rank modulation schemes, we introduce the notion of balanced permutations and derive the capacity of balanced permutation codes. We also describe simple interleaving methods for permutation code constructions and show that they approach capacity

cs.IT↗

arXiv2016

A new correlation clustering method for cancer mutation analysis

Cancer genomes exhibit a large number of different alterations that affect many genes in a diverse manner. It is widely believed that these alterations follow combinatorial patterns that have a strong connection with the underlying molecular interaction networks and functional pathways. A better understanding of the generative mechanisms behind the mutation rules and their influence on gene communities is of great importance for the process of driver mutations discovery and for identification of network modules related to cancer development and progression. We developed a new method for cancer mutation pattern analysis based on a constrained form of correlation clustering. Correlation clustering is an agnostic learning method that can be used for general community detection problems in which the number of communities or their structure is not known beforehand. The resulting algorithm, named $C^3$, leverages mutual exclusivity of mutations, patient coverage, and driver network concentration principles; it accepts as its input a user determined combination of heterogeneous patient data, such as that available from TCGA (including mutation, copy number, and gene expression information), and creates a large number of clusters containing mutually exclusive mutated genes in a particular type of cancer. The cluster sizes may be required to obey some useful soft size constraints, without impacting the computational complexity of the algorithm. To test $C^3$, we performed a detailed analysis on TCGA breast cancer and glioblastoma data and showed that our algorithm outperforms the state-of-the-art CoMEt method in terms of discovering mutually exclusive gene modules and identifying driver genes. Our $C^3$ method represents a unique tool for efficient and reliable identification of mutation patterns and driver pathways in large-scale cancer genomics studies.

cs.LG↗

arXiv2015

Codes for DNA Storage Channels

We consider the problem of assembling a sequence based on a collection of its substrings observed through a noisy channel. The mathematical basis of the problem is the construction and design of sequences that may be discriminated based on a collection of their substrings observed through a noisy channel. We explain the connection between the sequence reconstruction problem and the problem of DNA synthesis and sequencing, and introduce the notion of a DNA storage channel. We analyze the number of sequence equivalence classes under the channel mapping and propose new asymmetric coding techniques to combat the effects of synthesis and sequencing noise. In our analysis, we make use of restricted de Bruijn graphs and Ehrhart theory for rational polytopes.

cs.IT↗

arXiv2015

A Perspective on Future Research Directions in Information Theory

Information theory is rapidly approaching its 70th birthday. What are promising future directions for research in information theory? Where will information theory be having the most impact in 10-20 years? What new and emerging areas are ripe for the most impact, of the sort that information theory has had on the telecommunications industry over the last 60 years? How should the IEEE Information Theory Society promote high-risk new research directions and broaden the reach of information theory, while continuing to be true to its ideals and insisting on the intellectual rigor that makes its breakthroughs so powerful? These are some of the questions that an ad hoc committee (composed of the present authors) explored over the past two years. We have discussed and debated these questions, and solicited detailed inputs from experts in fields including genomics, biology, economics, and neuroscience. This report is the result of these discussions.

cs.IT↗

arXiv2015

DNA-Based Storage: Trends and Methods

We provide an overview of current approaches to DNA-based storage system design and accompanying synthesis, sequencing and editing methods. We also introduce and analyze a suite of new constrained coding schemes for both archival and random access DNA storage channels. The mathematical basis of our work is the construction and design of sequences over discrete alphabets that avoid pre-specified address patterns, have balanced base content, and exhibit other relevant substring constraints. These schemes adapt the stored signals to the DNA medium and thereby reduce the inherent error-rate of the system.

cs.ET↗

arXiv2015

Code Construction and Decoding Algorithms for Semi-Quantitative Group Testing with Nonuniform Thresholds

We analyze a new group testing scheme, termed semi-quantitative group testing, which may be viewed as a concatenation of an adder channel and a discrete quantizer. Our focus is on non-uniform quantizers with arbitrary thresholds. For the most general semi-quantitative group testing model, we define three new families of sequences capturing the constraints on the code design imposed by the choice of the thresholds. The sequences represent extensions and generalizations of Bh and certain types of super-increasing and lexicographically ordered sequences, and they lead to code structures amenable for efficient recursive decoding. We describe the decoding methods and provide an accompanying computational complexity and performance analysis.

cs.IT↗

arXiv2015

Poisson Group Testing: A Probabilistic Model for Boolean Compressed Sensing

We introduce a novel probabilistic group testing framework, termed Poisson group testing, in which the number of defectives follows a right-truncated Poisson distribution. The Poisson model has a number of new applications, including dynamic testing with diminishing relative rates of defectives. We consider both nonadaptive and semi-adaptive identification methods. For nonadaptive methods, we derive a lower bound on the number of tests required to identify the defectives with a probability of error that asymptotically converges to zero; in addition, we propose test matrix constructions for which the number of tests closely matches the lower bound. For semi-adaptive methods, we describe a lower bound on the expected number of tests required to identify the defectives with zero error probability. In addition, we propose a stage-wise reconstruction algorithm for which the expected number of tests is only a constant factor away from the lower bound. The methods rely only on an estimate of the average number of defectives, rather than on the individual probabilities of subjects being defective.

cs.IT↗

arXiv2015

Correlation Clustering with Constrained Cluster Sizes and Extended Weights Bounds

We consider the problem of correlation clustering on graphs with constraints on both the cluster sizes and the positive and negative weights of edges. Our contributions are twofold: First, we introduce the problem of correlation clustering with bounded cluster sizes. Second, we extend the regime of weight values for which the clustering may be performed with constant approximation guarantees in polynomial time and apply the results to the bounded cluster size problem.

cs.LG↗

arXiv2015

A Rewritable, Random-Access DNA-Based Storage System

We describe the first DNA-based storage architecture that enables random access to data blocks and rewriting of information stored at arbitrary locations within the blocks. The newly developed architecture overcomes drawbacks of existing read-only methods that require decoding the whole file in order to read one data fragment. Our system is based on new constrained coding techniques and accompanying DNA editing methods that ensure data reliability, specificity and sensitivity of access, and at the same time provide exceptionally high data storage capacity. As a proof of concept, we encoded parts of the Wikipedia pages of six universities in the USA, and selected and edited parts of the text written in DNA corresponding to three of these schools. The results suggest that DNA is a versatile media suitable for both ultrahigh density archival and rewritable storage applications.

cs.IT↗

arXiv2015

Codes for DNA Sequence Profiles

We consider the problem of storing and retrieving information from synthetic DNA media. The mathematical basis of the problem is the construction and design of sequences that may be discriminated based on their collection of substrings observed through a noisy channel. This problem of reconstructing sequences from traces was first investigated in the noiseless setting under the name of "Markov type" analysis. Here, we explain the connection between the reconstruction problem and the problem of DNA synthesis and sequencing, and introduce the notion of a DNA storage channel. We analyze the number of sequence equivalence classes under the channel mapping and propose new asymmetric coding techniques to combat the effects of synthesis and sequencing noise. In our analysis, we make use of restricted de Bruijn graphs and Ehrhart theory for rational polytopes.

cs.IT↗

arXiv2014

Computing Similarity Distances Between Rankings

We address the problem of computing distances between rankings that take into account similarities between candidates. The need for evaluating such distances is governed by applications as diverse as rank aggregation, bioinformatics, social sciences and data storage. The problem may be summarized as follows: Given two rankings and a positive cost function on transpositions that depends on the similarity of the candidates involved, find a smallest cost sequence of transpositions that converts one ranking into another. Our focus is on costs that may be described via special metric-tree structures and on complete rankings modeled as permutations. The presented results include a quadratic-time algorithm for finding a minimum cost decomposition for simple cycles, and a quadratic-time, $4/3$-approximation algorithm for permutations that contain multiple cycles. The proposed methods rely on investigating a newly introduced balancing property of cycles embedded in trees, cycle-merging methods, and shortest path optimization techniques.

cs.DS↗

arXiv2014

Synchronizing Edits in Distributed Storage Networks

We consider the problem of synchronizing data in distributed storage networks under an edit model that includes deletions and insertions. We present two modifications of MDS, regenerating and locally repairable codes that allow updates in the parity-check values to be performed with one round of communication at low bit rates and using small storage overhead. Our main contributions are novel protocols for synchronizing both hot and semi-static data and protocols for data deduplication applications, based on intermediary permutation, Vandermonde and Cauchy matrix coding.

cs.IT↗

arXiv2014

String Reconstruction from Substring Compositions

Motivated by mass-spectrometry protein sequencing, we consider a simply-stated problem of reconstructing a string from the multiset of its substring compositions. We show that all strings of length 7, one less than a prime, or one less than twice a prime, can be reconstructed uniquely up to reversal. For all other lengths we show that reconstruction is not always possible and provide sometimes-tight bounds on the largest number of strings with given substring compositions. The lower bounds are derived by combinatorial arguments and the upper bounds by algebraic considerations that precisely characterize the set of strings with the same substring compositions in terms of the factorization of bivariate polynomials. The problem can be viewed as a combinatorial simplification of the turnpike problem, and its solution may shed light on this long-standing problem as well. Using well known results on transience of multi-dimensional random walks, we also provide a reconstruction algorithm that reconstructs random strings over alphabets of size $\ge4$ in optimal near-quadratic time.

cs.DM↗

arXiv2014

Synchronizing Rankings via Interactive Communication

We consider the problem of exact synchronization of two rankings at remote locations connected by a two-way channel. Such synchronization problems arise when items in the data are distinguishable, as is the case for playlists, tasklists, crowdvotes and recommender systems rankings. Our model accounts for different constraints on the communication throughput of the forward and feedback links, resulting in different anchoring, syndrome and checksum computation strategies. Information editing is assumed of the form of deletions, insertions, block deletions/insertions, translocations and transpositions. The protocols developed under the given model are order-optimal with respect to genie aided lower bounds.

cs.IT↗

arXiv2013

Multipermutation Codes in the Ulam Metric for Nonvolatile Memories

We address the problem of multipermutation code design in the Ulam metric for novel storage applications. Multipermutation codes are suitable for flash memory where cell charges may share the same rank. Changes in the charges of cells manifest themselves as errors whose effects on the retrieved signal may be measured via the Ulam distance. As part of our analysis, we study multipermutation codes in the Hamming metric, known as constant composition codes. We then present bounds on the size of multipermutation codes and their capacity, for both the Ulam and the Hamming metrics. Finally, we present constructions and accompanying decoders for multipermutation codes in the Ulam metric.

cs.IT↗

arXiv2013

MCUIUC -- A New Framework for Metagenomic Read Compression

Metagenomics is an emerging field of molecular biology concerned with analyzing the genomes of environmental samples comprising many different diverse organisms. Given the nature of metagenomic data, one usually has to sequence the genomic material of all organisms in a batch, leading to a mix of reads coming from different DNA sequences. In deep high-throughput sequencing experiments, the volume of the raw reads is extremely high, frequently exceeding 600 Gb. With an ever increasing demand for storing such reads for future studies, the issue of efficient metagenomic compression becomes of paramount importance. We present the first known approach to metagenome read compression, termed MCUIUC (Metagenomic Compression at UIUC). The gist of the proposed algorithm is to perform classification of reads based on unique organism identifiers, followed by reference-based alignment of reads for individually identified organisms, and metagenomic assembly of unclassified reads. Once assembly and classification are completed, lossless reference based compression is performed via positional encoding. We evaluate the performance of the algorithm on moderate sized synthetic metagenomic samples involving 15 randomly selected organisms and describe future directions for improving the proposed compression method.

q-bio.GN↗

arXiv2013

MetaPar: Metagenomic Sequence Assembly via Iterative Reclassification

We introduce a parallel algorithmic architecture for metagenomic sequence assembly, termed MetaPar, which allows for significant reductions in assembly time and consequently enables the processing of large genomic datasets on computers with low memory usage. The gist of the approach is to iteratively perform read (re)classification based on phylogenetic marker genes and assembler outputs generated from random subsets of metagenomic reads. Once a sufficiently accurate classification within genera is performed, de novo metagenomic assemblers (such as Velvet or IDBA-UD) or reference based assemblers may be used for contig construction. We analyze the performance of MetaPar on synthetic data consisting of 15 randomly chosen species from the NCBI database through the effective gap and effective coverage metrics.

q-bio.QM↗