Demo Data from VLDB 2026 / reviewers in the wild / expert
Vida Ravanmehr
dblp:71/10504
· DBLP profile ↗
8ranked-venue papers
5as first author
1since 2021 · last 2023
0000-0002-3971-1083ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 6 · 3 first-author · 1 since 2021Theory of computation · 2 · 2 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.
| Interdisciplinary, comprehensive, and emerging computing
2 papers |
Bioinformatics and computational biology · 73% Computational science and engineering · 27% |
Topics — the 5 heaviest of 6, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › network bioinformatics › biological network analysis
biological knowledge graph |
0.7 | 1 | 2023 | KG-Hub - building and exchanging biological knowledge graphs · Bioinform. 2023 |
Bioinformatics and computational biology › genomics
genomic data compression |
0.3 | 1 | 2018 | ChIPWig: a random access-enabling lossless and lossy compression method for ChIP-seq data · Bioinform. 2018 |
Computational science and engineering
graph learning |
0.2 | 1 | 2023 | KG-Hub - building and exchanging biological knowledge graphs · Bioinform. 2023 |
Computational science and engineering › graph learning
link prediction |
0.2 | 1 | 2023 | KG-Hub - building and exchanging biological knowledge graphs · Bioinform. 2023 |
Bioinformatics and computational biology
epigenomics |
0.1 | 1 | 2018 | ChIPWig: a random access-enabling lossless and lossy compression method for ChIP-seq data · Bioinform. 2018 |
Methods — techniques the papers use, named apart from their topics
node embedding · 0.7graph machine learning · 0.7extract-transform-load · 0.7optimal point density design · 0.3nonuniform quantization · 0.3
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2023 | KG-Hub - building and exchanging biological knowledge graphsabstractMOTIVATION: Knowledge graphs (KGs) are a powerful approach for integrating heterogeneous data and making inferences in biology and many other domains, but a coherent solution for constructing, exchanging, and facilitating the downstream use of KGs is lacking. RESULTS: Here we present KG-Hub, a platform that enables standardized construction, exchange, and reuse of KGs. Features include a simple, modular extract-transform-load pattern for producing graphs compliant with Biolink Model (a high-level data model for standardizing biological data), easy integration of any OBO (Open Biological and Biomedical Ontologies) ontology, cached downloads of upstream data sources, versioned and automatically updated builds with stable URLs, web-browsable storage of KG artifacts on cloud infrastructure, and easy reuse of transformed subgraphs across projects. Current KG-Hub projects span use cases including COVID-19 research, drug repurposing, microbial-environmental interactions, and rare disease research. KG-Hub is equipped with tooling to easily analyze and manipulate KGs. KG-Hub is also tightly integrated with graph machine learning (ML) tools which allow automated graph ML, including node embeddings and training of models for link prediction and node classification. AVAILABILITY AND IMPLEMENTATION: https://kghub.org. J. Harry Caufield, Tim E. Putman, Kevin Schaper, Deepak R. Unni, Harshad Hegde, Tiffany Callahan, Luca Cappelletti, Sierra A. T. Moxon, Vida Ravanmehr, Seth Carbon, Lauren E. Chan, Katherina G. Cortes, Kent A. Shefchek, Glass Elsarboukh, James P. Balhoff, Tommaso Fontana, Nicolas Matentzoglu, Richard M. Bruskiewich, Anne E. Thessen, Nomi L. Harris, Monica C. Munoz-Torres, Melissa A. Haendel, Peter N. Robinson, Marcin P. Joachimiak, Chris Mungall, Justin T. Reese |
Bioinform. | 9 |
| 2018 | ChIPWig: a random access-enabling lossless and lossy compression method for ChIP-seq dataabstractMotivation: Chromatin immunoprecipitation sequencing (ChIP-seq) experiments are inexpensive and time-efficient, and result in massive datasets that introduce significant storage and maintenance challenges. To address the resulting Big Data problems, we propose a lossless and lossy compression framework specifically designed for ChIP-seq Wig data, termed ChIPWig. ChIPWig enables random access, summary statistics lookups and it is based on the asymptotic theory of optimal point density design for nonuniform quantizers. Results: We tested the ChIPWig compressor on 10 ChIP-seq datasets generated by the ENCODE consortium. On average, lossless ChIPWig reduced the file sizes to merely 6% of the original, and offered 6-fold compression rate improvement compared to bigWig. The lossy feature further reduced file sizes 2-fold compared to the lossless mode, with little or no effects on peak calling and motif discovery using specialized NarrowPeaks methods. The compression and decompression speed rates are of the order of 0.2 sec/MB using general purpose computers. Availability and implementation: The source code and binaries are freely available for download at https://github.com/vidarmehr/ChIPWig-v2, implemented in C ++. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online. Vida Ravanmehr, Minji Kim 0007, Zhiying Wang 0001, Olgica Milenkovic |
Bioinform. | 1 |
| 2018 | Paired threshold graphs
Vida Ravanmehr, Gregory J. Puleo, Sadegh Bolouki, Olgica Milenkovic |
Discret. Appl. Math. | 1 |
| 2016 | Doubly threshold graphs for social network modelingabstractThreshold graphs are recursive deterministic network models that capture properties of certain social and economic interactions. One drawback of these graph families is that they they have limited constrained generative attachment rules. To mitigate this problem, we introduce a new class of graphs termed Doubly Threshold (DT) graphs which may be succinctly described through vertex weights that govern the existence of edges via two inequalities. One inequality imposes the constraint that the sum of weights of adjacent vertices has to exceed a specified threshold. The second inequality ensures that adjacent vertices have a bounded difference of their weights. We provide a succinct characterization and decomposition of DT graphs and analyze their forbidden induced subgraphs which we compare to those of known social networks. We also present a method for performing vertex weight assignments on DT graphs that satisfy the defining constraints. Vida Ravanmehr, Sadegh Bolouki, Gregory J. Puleo, Olgica Milenkovic |
ITW | 1 |
| 2014 | GBP-based detection and symmetric information rate for rectangular-grain TDMR modelabstractTwo dimensional magnetic recording (TDMR) is a new paradigm in data storage which envisions densities up to 10 Tb/in2as a result of drastically reducing bit to grain ratio. In order to reach this goal aggressive write (shingled writing) and read process are used in TDMR. Kavcic et al. proposed a simple magnetic grain model called the granular tiling model which captures the essence of read/write process in TDMR. Capacity bounds for this model indicate that 0.6 user bit per grain densities are possible, however, previous attempt to reach capacities are not close to the channel capacity. In this paper, we provide a truly two-dimensional detection scheme for the granular tiling model based on generalized belief propagation (GBP). Factor graph interpretation of the detection problem is provided and formulated in this paper. Then, GBP is employed to compute marginal a posteriori probabilities for the constructed factor graph. Simulation results show huge improvements in detection. A lower bound on the symmetric information rate (SIR) is also derived for this model based on GBP detector. Mehrdad Khatami, Vida Ravanmehr, Bane Vasic |
ISIT | 2 |
| 2014 | Check-hybrid GLDPC codes: Systematic elimination of trapping sets by super checksabstractIn this paper, we propose a new approach to constructing a class of check-hybrid generalized low-density parity-check (GLDPC) codes which are free of small trapping sets. This approach is based on converting selected checks of an LDPC code involving a trapping set to super checks corresponding to a shorter error correcting component code. In particular, we follow two goals in constructing the check-hybrid GLDPC codes: First, the super checks are replaced based on the knowledge of trapping sets of the global LDPC code. We show that by converting only some single checks to super checks the decoder corrects the errors on a trapping set and hence eliminates the trapping set. Second, the number of super checks required for eliminating certain trapping sets is minimized to reduce the rate-loss. We first give an algorithm to find a set of critical checks in a trapping set of an LDPC code and then we provide some upper bounds on the minimum number of critical checks needed to eliminate certain trapping sets in the parity-check matrix of an LDPC code. A possible fixed set for a class of check-hybrid codes is also given. Vida Ravanmehr, David Declercq, Bane Vasic |
ISIT | 1 |
| 2012 | Quasi-cyclic codes exhibiting the gene regulatory network of the cell cycleabstractWe present an artificial Boolean network exhibiting the behaviour similar to that of the cell cycle: three phases and checkpoints between them. The phases follow the increase of the cell mass, while checkpoints ensure that internal errors are corrected before moving to the next phase. The network can tolerate up to one gene mutation and one transient error in gene expressions. It has only 6 genes and is the smallest and simplest network with such behavior. It is based on a special type of error correction codes, resulting in an elegant and symmetric network topology and highly symmetric attractor basin. Vida Ravanmehr, Bane Vasic |
CIBCB | 1 |
| 2012 | An Information Theoretic Approach to Constructing Robust Boolean Gene Regulatory NetworksabstractWe introduce a class of finite systems models of gene regulatory networks exhibiting behavior of the cell cycle. The model is an extension of a Boolean network model. The system spontaneously cycles through a finite set of internal states, tracking the increase of an external factor such as cell mass, and also exhibits checkpoints in which errors in gene expression levels due to cellular noise are automatically corrected. We present a 7-gene network based on Projective Geometry codes, which can correct, at every given time, one gene expression error. The topology of a network is highly symmetric and requires using only simple Boolean functions that can be synthesized using genes of various organisms. The attractor structure of the Boolean network contains a single cycle attractor. It is the smallest nontrivial network with such high robustness. The methodology allows construction of artificial cell cycle gene regulatory networks with the number of phases larger than in natural cell cycle. Bane Vasic, Vida Ravanmehr, Anantha Raman Krishnan |
IEEE ACM Trans. Comput. Biol. Bioinform. | 2 |