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pro vyhledávání: '"Anett Fekete"'
Autor:
Anett FEKETE, Zoltán PORKOLÁB
Publikováno v:
Studia Universitatis Babes-Bolyai: Series Informatica, Vol 68, Iss 1 (2023)
Program comprehension is a continuously important topic in computer science since the spread of personal computers, and several program comprehension models have been identified as possible directions of active code comprehension. There has been litt
Externí odkaz:
https://doaj.org/article/a27ece6dd4d4410e87896fa82b8f7b95
Autor:
Anett Fekete, Zoltán Porkolab
Publikováno v:
2022 IEEE 16th International Scientific Conference on Informatics (Informatics).
Publikováno v:
INTED2022 Proceedings.
Publikováno v:
MIPRO
Developers' fluctuation in the lifetime of a software product might deteriorate the understanding of the source code to a level where developer expertise of some modules drops to a dangerously low point. It is important for the project management to
Autor:
Anett Fekete, Mate Cserep
Publikováno v:
Computers & Geosciences. 156:104900
As the utilization of LiDAR (Light Detection and Ranging) is getting more affordable and available for a wider audience, the analysis of point clouds constructed by laser scanning is earning more attention. Airborne LiDAR is especially useful in the
Autor:
Béla Melegh, László Balikó, Kim Boycott, Kinga Hadzsiev, Ferenc Nagy, Mónika Szőts, Anett Fekete
Publikováno v:
Orvosi Hetilap. 158:1681-1684
Abstract: In a patient with marked symptoms of Huntington disease after the huntingtin testing, which gave normal result, a whole exome sequencing (WES) has been performed based on an international collaboration. A homozygous G>A nucleotid change in
Autor:
Márta Czakó, András Szabó, Kinga Hadzsiev, Anett Fekete, Béla Melegh, Judit Bene, Ágnes Till, Judith Zima
Publikováno v:
Seizure. 74
Purpose The vast majority of mutations responsible for epilepsy syndromes such as genetic epilepsy with febrile seizures plus (GEFS+) and Dravet syndrome (DS) occur in the gene encoding the type 1 alpha subunit of neuronal voltage-gated sodium channe
Publikováno v:
MIPRO
The maintenance of large, legacy software often results in higher development time and cost due to increasing size and complexity of the codebase and its documentation, their continuously eroding quality and fluctuation among developers. Code compreh
Autor:
Kinga, Hadzsiev, Mónika, Szőts, Anett, Fekete, László, Balikó, Kim, Boycott, Ferenc, Nagy, Béla, Melegh
Publikováno v:
Orvosi hetilap. 158(42)
In a patient with marked symptoms of Huntington disease after the huntingtin testing, which gave normal result, a whole exome sequencing (WES) has been performed based on an international collaboration. A homozygous GA nucleotid change in the exon 34
Autor:
Anett, Fekete, Kinga, Hadzsiev, Judit, Bene, Antónia, Nászai, Petra, Mátyás, Ágnes, Till, Béla, Melegh
Publikováno v:
Orvosi hetilap. 158(12)
This article presents the case of a 62-year-old mother and her 41-year-old daughter, who have had severe neurological symptoms for a few decades. After a long investigation period the definite diagnosis of MERRF syndrome was confirmed. After DNA isol