Zobrazeno 1 - 10
of 963
pro vyhledávání: '"Laemmle, A."'
Real-world applications of machine learning models are often subject to legal or policy-based regulations. Some of these regulations require ensuring the validity of the model, i.e., the approximation error being smaller than a threshold. A global me
Externí odkaz:
http://arxiv.org/abs/2406.07474
Surrogate models based on machine learning methods have become an important part of modern engineering to replace costly computer simulations. The data used for creating a surrogate model are essential for the model accuracy and often restricted due
Externí odkaz:
http://arxiv.org/abs/2310.00110
Autor:
Laemmle-Ruff, Ingrid, Fryk, Jesse J., Shenton, Priya, Clothier, Hazel J., Parsons, Sarah, Iles, Linda, White, Clare, Murray, Michael, Buttery, Jim, Crawford, Nigel W.
Publikováno v:
In Vaccine 2 December 2024 42(26)
Autor:
Barra, Diana, Donadio, Carlo, Lämmle, Luca, Perez Filho, Archimedes, Stamatopoulos, Leonidas, Valente, Alessio, Kontopoulos, Nikolaos, Parisi, Roberta, Stanislao, Corrado, Aiello, Giuseppe
Publikováno v:
In Quaternary International 15 November 2024 710:66-94
Autor:
Kropp, Michael, Lämmle, Manuel, Herkel, Sebastian, Henning, Hans-Martin, Velte-Schäfer, Andreas
Publikováno v:
In Energy & Buildings 1 February 2025 328
Publikováno v:
In Aquaculture 15 January 2025 594
Autor:
Ayer, Joaquim Ernesto Bernardes, Lämmle, Luca, Mincato, Ronaldo Luiz, Donadio, Carlo, Avramidis, Pavlos, Pereira, Sueli Yoshinaga
Publikováno v:
In Groundwater for Sustainable Development August 2024 26
Publikováno v:
In Molecular Genetics and Metabolism August 2024 142(4)
Autor:
Déborah Mathis, Jasmine Koch, Sophie Koller, Kay Sauter, Christa Flück, Anne-Christine Uldry, Patrick Forny, D. Sean Froese, Alexander Laemmle
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 39, Iss , Pp 101066- (2024)
Mitochondrial malate dehydrogenase 2 (MDH2) is crucial to cellular energy generation through direct participation in the tricarboxylic acid (TCA) cycle and the malate aspartate shuttle (MAS). Inherited MDH2 deficiency is an ultra-rare metabolic disea
Externí odkaz:
https://doaj.org/article/56cf900502d140459292f6c91fed6cfd
Autor:
Mathis, Déborah, Koch, Jasmine, Koller, Sophie, Sauter, Kay, Flück, Christa, Uldry, Anne-Christine, Forny, Patrick, Froese, D. Sean, Laemmle, Alexander
Publikováno v:
In Molecular Genetics and Metabolism Reports June 2024 39