Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Peter Sarkozy"'
Autor:
Andrea Vereczkei, Zsolt Demetrovics, Anna Szekely, Peter Sarkozy, Peter Antal, Agnes Szilagyi, Maria Sasvari-Szekely, Csaba Barta
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e66592 (2013)
BACKGROUND: Heroin dependence is a debilitating psychiatric disorder with complex inheritance. Since the dopaminergic system has a key role in rewarding mechanism of the brain, which is directly or indirectly targeted by most drugs of abuse, we focus
Externí odkaz:
https://doaj.org/article/98c77ee9fa364b83b6355b03727ff7d0
Publikováno v:
Orvosi Hetilap. 162:1079-1088
Összefoglaló. A fejlett társadalmak egészségügyi rendszereinek legnagyobb kihívását az öregedéssel összefüggő, korfüggő betegségek jelentik. Annak megértéséhez, hogy az egyes genetikai variánsoknak mi a szerepük egy korfüggő b
Publikováno v:
IFMBE Proceedings ISBN: 9789811051210
Oxford Nanopore Technologies’ (ONT) MinION device is capable of reading single molecule DNA strands tens of thousands of bases long, by passing a strand through a nanopore and recording the changes in electric current. The error rate of the platfor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::450e376547454fac5711515b3f78fbd1
https://doi.org/10.1007/978-981-10-5122-7_61
https://doi.org/10.1007/978-981-10-5122-7_61
Autor:
Maria Sasvari-Szekely, Peter Sarkozy, Zsofia Nemoda, Péter Antal, Zsolt Demetrovics, Anna Szekely, Gábor Varga
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :281-288
Twin studies suggest 45% heritability of trait impulsivity. Results from candidate gene studies to date are contradictory; impulsivity phenotypes were measured by different behavioral and questionnaire methods related either to the dopaminergic or to
Publikováno v:
BMC Genomics
Background The low concordance between different variant calling methods still poses a challenge for the wide-spread application of next-generation sequencing in research and clinical practice. A wide range of variant annotations can be used for filt
Publikováno v:
First European Biomedical Engineering Conference for Young Investigators ISBN: 9789812875723
Variant calling, the identification of DNA sites that differ from a reference sequence using Next Generation Sequencing (NGS) methods is still an inherently error prone process. Quality scores of variant calling results in NGS studies is a key utilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c477c6d24f3a34ade8747d82db007a25
https://doi.org/10.1007/978-981-287-573-0_11
https://doi.org/10.1007/978-981-287-573-0_11
Publikováno v:
Periodica Polytechnica Electrical Engineering and Computer Science. 61:231
Electronic, nanopore based single molecule real-time DNA sequencing technology offers very long, albeit lower accuracy reads in sharp contrast to existing next-generation sequencing methods, which offer short, high-accuracy reads in abundance. We pro
Autor:
András Falus, András Gézsi, Gergely Hajós, Gabor Hullam, Peter Sarkozy, Péter Antal, Csaba Szalai, András Millinghoffer
Publikováno v:
Probabilistic Graphical Models for Genetics, Genomics, and Postgenomics ISBN: 0198709021
Probabilistic Graphical Models for Genetics, Genomics, and Postgenomics
Probabilistic Graphical Models for Genetics, Genomics, and Postgenomics
The relative scarcity of the results reported by genetic association studies (GAS) prompted many research directions. Despite the centrality of the concept of association in GASs, refined concepts of association are missing; meanwhile, various featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e9ec4f245ad7ba10f37786919ee8428
https://doi.org/10.1093/acprof:oso/9780198709022.003.0013
https://doi.org/10.1093/acprof:oso/9780198709022.003.0013
Autor:
László Tamás, Peter Sarkozy, Zoltán Takácsi-Nagy, Gergely Léránt, Maria Godeny, Erika Toth, Laszlo Javor, Gábor Polony, András Boér
Publikováno v:
Pathology oncology research : POR. 21(4)
Pilot studies have shown promising results in characterizing head and neck tumors (HNT) using dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI), differentiating between malignant and benign lesions and evaluating changes in response to c
Autor:
András Gézsi, Zsuzsanna Pál, András Millinghoffer, Gábor Hullám, Peter Sarkozy, Edit I. Buzás, Sanjeev K. Srivastava, Bence Bolgár, Péter Antal
Publikováno v:
Methods in Molecular Biology ISBN: 9781493904037
Rich dependency structures are often formed in genetic association studies between the phenotypic, clinical, and environmental descriptors. These descriptors may not be standardized, and may encompass various disease definitions and clinical endpoint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ddb8f4a19937cbf37501ceb15cfbb72
https://doi.org/10.1007/978-1-4939-0404-4_14
https://doi.org/10.1007/978-1-4939-0404-4_14