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Maya Levy

dblp:204/4385 · DBLP profile ↗
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3ranked-venue papers
3as first author
0since 2021 · last 2020
—ORCID · conflict

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-authorTheory of computation · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Theoretical computer science
1 paper
Coding theory · 100%
Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
Storage systems · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › single-cell analysis
single-cell genomics
0.412020
Inferring cellular heterogeneity of associations from single cell genomics · Bioinform. 2020
Coding theory
constrained coding
0.412019
Mutually Uncorrelated Codes for DNA Storage · IEEE Trans. Inf. Theory 2019
Coding theory
error-correcting codes
0.412019
Mutually Uncorrelated Codes for DNA Storage · IEEE Trans. Inf. Theory 2019
Coding theory › constrained coding
runlength-limited codes
0.412019
Mutually Uncorrelated Codes for DNA Storage · IEEE Trans. Inf. Theory 2019
Storage systems › storage devices › molecular data storage
DNA storage
0.112019
Mutually Uncorrelated Codes for DNA Storage · IEEE Trans. Inf. Theory 2019
Storage systems
random access
0.112019
Mutually Uncorrelated Codes for DNA Storage · IEEE Trans. Inf. Theory 2019

Methods — techniques the papers use, named apart from their topics

edit distance · 0.8code construction · 0.8statistical association testing · 0.4
YearPublicationVenuePosition
2020 Inferring cellular heterogeneity of associations from single cell genomics
abstract
MOTIVATION: Cell-to-cell variation has uncovered associations between cellular phenotypes. However, it remains challenging to address the cellular diversity of such associations. RESULTS: Here, we do not rely on the conventional assumption that the same association holds throughout the entire cell population. Instead, we assume that associations may exist in a certain subset of the cells. We developed CEllular Niche Association (CENA) to reliably predict pairwise associations together with the cell subsets in which the associations are detected. CENA does not rely on predefined subsets but only requires that the cells of each predicted subset would share a certain characteristic state. CENA may therefore reveal dynamic modulation of dependencies along cellular trajectories of temporally evolving states. Using simulated data, we show the advantage of CENA over existing methods and its scalability to a large number of cells. Application of CENA to real biological data demonstrates dynamic changes in associations that would be otherwise masked. AVAILABILITY AND IMPLEMENTATION: CENA is available as an R package at Github: https://github.com/mayalevy/CENA and is accompanied by a complete set of documentations and instructions. CONTACT: [email protected]. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Maya Levy, Amit Frishberg, Irit Gat-Viks
Bioinform.1
2019 Mutually Uncorrelated Codes for DNA Storage
abstract
Mutually uncorrelated (MU) codes are a class of codes in which no proper prefix of one codeword is a suffix of another codeword. These codes were originally studied for synchronization purposes and recently, Yazdi et al. showed their applicability to enable random access in DNA storage. In this paper,we follow the research of Yazdi et al. and study MU codes along with their extensions to correct errors and balanced codes. We first review a well-known construction of MU codes and study the asymptotic behavior of its cardinality. This task is accomplished by studying a special class of run-length limited codes that impose the longest run of zeros to be at most some function of the codewords length. We also present an efficient algorithm for this class of constrained codes and show how to use this analysis for MU codes. Next, we extend the results on the run-length limited codes in order to study (dh, dm)-MU codes that impose a minimum Hamming distance of dh between different codewords and dmbetween prefixes and suffixes. In particular, we show an efficient construction of these codes with nearly optimal redundancy. We also provide similar results for the edit distance and balanced MU codes. Last, we draw connections to the problems of comma-free and prefix synchronized codes.
Maya Levy, Eitan Yaakobi
IEEE Trans. Inf. Theory1
2017 Mutually uncorrelated codes for DNA storage
abstract
Mutually Uncorrelated (MU) codes are a class of codes in which no proper prefix of one codeword is a suffix of another codeword. These codes were originally studied for synchronization purposes and recently, Yazdi et al. showed their applicability to enable random access in DNA storage. In this work we follow the research of Yazdi et al. and study MU codes along with their extensions to correct errors and balanced codes. We first review a well known construction of MU codes and study the asymptotic behavior of its cardinality. Then, we present an efficient algorithm for MU codes with linear encoding and decoding complexity. Next, we extend these results for (dh, dm)-MU codes that impose a minimum Hamming distance of dh between different codewords and dmbetween prefixes and suffixes. Particularly we show an efficient construction of these codes with nearly optimal redundancy and draw connections to the problem of comma-free and prefix synchronized codes. Lastly, we provide similar results for the edit distance and balanced MU codes.
Maya Levy, Eitan Yaakobi
ISIT1