Institution
Helsinki Institute for Information Technology
Facility•Espoo, Finland•
About: Helsinki Institute for Information Technology is a facility organization based out in Espoo, Finland. It is known for research contribution in the topics: Population & Bayesian network. The organization has 630 authors who have published 1962 publications receiving 63426 citations.
Papers published on a yearly basis
Papers
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TL;DR: It is found that text chat always increased heart rate synchrony but HR visualization only with non-co-located dyads and physiological linkage was strongly connected to self-reported social presence.
Abstract: We investigated how technologically mediating two different components of emotion – communicative expression and physiological state – to group members affects physiological linkage and self-reported feelings in a small group during video viewing. In different conditions the availability of second screen text chat (communicative expression) and visualization of group level physiological heart rates and their dyadic linkage (physiology) was varied. Within this four person group two participants formed a physically co-located dyad and the other two were individually situated in two separate rooms. We found that text chat always increased heart rate synchrony but HR visualization only with non-co-located dyads. We also found that physiological linkage was strongly connected to self-reported social presence. The results encourage further exploration of the possibilities of sharing group member’s physiological components of emotion by technological means to enhance mediated communication and strengthen social presence.
17 citations
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08 Jul 2010TL;DR: This work presents the first exponential family multi-view learning methods of the partial least squares and canonical correlation analysis, based on a unified representation of EPCA as matrix factorization of the natural parameters of exponential family.
Abstract: Exponential family extensions of principal component analysis (EPCA) have received a considerable amount of attention in recent years, demonstrating the growing need for basic modeling tools that do not assume the squared loss or Gaussian distribution. We extend the EPCA model toolbox by presenting the first exponential family multi-view learning methods of the partial least squares and canonical correlation analysis, based on a unified representation of EPCA as matrix factorization of the natural parameters of exponential family. The models are based on a new family of priors that are generally usable for all such factorizations. We also introduce new inference strategies, and demonstrate how the methods outperform earlier ones when the Gaussianity assumption does not hold.
17 citations
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15 Jul 2019TL;DR: In this paper, the authors propose a Bayesian model for metabolic flux analysis, which couples all fluxes jointly together in a simple truncated multivariate posterior distribution, which reveals informative flux couplings.
Abstract: Motivation Metabolic flux balance analysis (FBA) is a standard tool in analyzing metabolic reaction rates compatible with measurements, steady-state and the metabolic reaction network stoichiometry. Flux analysis methods commonly place model assumptions on fluxes due to the convenience of formulating the problem as a linear programing model, while many methods do not consider the inherent uncertainty in flux estimates. Results We introduce a novel paradigm of Bayesian metabolic flux analysis that models the reactions of the whole genome-scale cellular system in probabilistic terms, and can infer the full flux vector distribution of genome-scale metabolic systems based on exchange and intracellular (e.g. 13C) flux measurements, steady-state assumptions, and objective function assumptions. The Bayesian model couples all fluxes jointly together in a simple truncated multivariate posterior distribution, which reveals informative flux couplings. Our model is a plug-in replacement to conventional metabolic balance methods, such as FBA. Our experiments indicate that we can characterize the genome-scale flux covariances, reveal flux couplings, and determine more intracellular unobserved fluxes in Clostridium acetobutylicum from 13C data than flux variability analysis. Availability and implementation The COBRA compatible software is available at github.com/markusheinonen/bamfa. Supplementary information Supplementary data are available at Bioinformatics online.
17 citations
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TL;DR: This work explores several complete and incomplete search techniques for finding minimal, or at least small, tile sets and also assess the reliability of the solutions obtained according to the kinetic Tile Assembly Model.
17 citations
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TL;DR: This work addresses the scalability limitations of the BF-based forwarding protocols by partitioning end-hosts into clusters by proposing several algorithms to do the partitioning so as to decrease the overall traffic in the network.
17 citations
Authors
Showing all 632 results
Name | H-index | Papers | Citations |
---|---|---|---|
Dimitri P. Bertsekas | 94 | 332 | 85939 |
Olli Kallioniemi | 90 | 353 | 42021 |
Heikki Mannila | 72 | 295 | 26500 |
Jukka Corander | 66 | 411 | 17220 |
Jaakko Kangasjärvi | 62 | 146 | 17096 |
Aapo Hyvärinen | 61 | 301 | 44146 |
Samuel Kaski | 58 | 522 | 14180 |
Nadarajah Asokan | 58 | 327 | 11947 |
Aristides Gionis | 58 | 292 | 19300 |
Hannu Toivonen | 56 | 192 | 19316 |
Nicola Zamboni | 53 | 128 | 11397 |
Jorma Rissanen | 52 | 151 | 22720 |
Tero Aittokallio | 52 | 271 | 8689 |
Juha Veijola | 52 | 261 | 19588 |
Juho Hamari | 51 | 176 | 16631 |