Vince Grolmusz

Prof. Vince Grolmusz

PIT Bioinformatics Group, Eötvös Loránd University, H-1117 Budapest, Hungary
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Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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12 December 2010 in Bioinformatics
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GIGábor Iván
Gábor Iván
Vince GrolmuszVince Grolmusz
Vince Grolmusz
Motivation: Enormous and constantly increasing quantity of biological information is represented in metabolic and in protein interaction network databases. Most of these data are freely accessible through large public depositories. The robust analysis of these resources needs novel technologies, being developed today. Results: Here we demonstrate a technique, originating from the PageRank computation for the World Wide Web, for analyzing large interaction networks. The method is fast, scalable and robust, and its capabilities are demonstrated on metabolic network data of the tuberculosis bacterium and the proteomics analysis of the blood of melanoma patients. Availability: The Perl script for computing the personalized PageRank in protein networks is available for non-profit research applications (together with sample input files) at the address: http://uratim.com/pp.zip Contact:grolmusz@cs.elte.hu. Supplementary information: Supplementary data are available at Bioinformatics online.


1 January 2014 in Gene
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Journal Article
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CKCsaba Kerepesi
Csaba Kerepesi
DBDániel Bánky
Dániel Bánky
Vince GrolmuszVince Grolmusz
Vince Grolmusz

15 September 2016 in Cognitive Neurodynamics
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BSBalázs Szalkai
Balázs Szalkai
CKCsaba Kerepesi
Csaba Kerepesi
BVBálint Varga
Bálint Varga
Vince GrolmuszVince Grolmusz
Vince Grolmusz

1 June 2015 in Information Processing Letters
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Vince GrolmuszVince Grolmusz
Vince Grolmusz

1 July 2015 in PLOS ONE
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Journal Article
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BSBalázs Szalkai
Balázs Szalkai
BVBálint Varga
Bálint Varga
Vince GrolmuszVince Grolmusz
Vince Grolmusz
Deep graph-theoretic ideas in the context with the graph of the World Wide Web led to the definition of Google’s PageRank and the subsequent rise of the most popular search engine to date. Brain graphs, or connectomes, are being widely explored today. We believe that non-trivial graph theoretic concepts, similarly as it happened in the case of the World Wide Web, will lead to discoveries enlightening the structural and also the functional details of the animal and human brains. When scientists examine large networks of tens or hundreds of millions of vertices, only fast algorithms can be applied because of the size constraints. In the case of diffusion MRI-based structural human brain imaging, the effective vertex number of the connectomes, or brain graphs derived from the data is on the scale of several hundred today. That size facilitates applying strict mathematical graph algorithms even for some hard-to-compute (or NP-hard) quantities like vertex cover or balanced minimum cut. In the present work we have examined brain graphs, computed from the data of the Human Connectome Project, recorded from male and female subjects between ages 22 and 35. Significant differences were found between the male and female structural brain graphs: we show that the average female connectome has more edges, is a better expander graph, has larger minimal bisection width, and has more spanning trees than the average male connectome. Since the average female brain weighs less than the brain of males, these properties show that the female brain has better graph theoretical properties, in a sense, than the brain of males. It is known that the female brain has a smaller gray matter/white matter ratio than males, that is, a larger white matter/gray matter ratio than the brain of males; this observation is in line with our findings concerning the number of edges, since the white matter consists of myelinated axons, which, in turn, roughly correspond to the connections in the brain graph. We have also found that the minimum bisection width, normalized with the edge number, is also significantly larger in the right and the left hemispheres in females: therefore, the differing bisection widths are independent from the difference in the number of edges.