Artificial neural networks modeling the in vitro rhizogenesis and acclimatization of Vitis vinifera L.

2010 ◽  
Vol 167 (15) ◽  
pp. 1226-1231 ◽  
Author(s):  
Jorge Gago ◽  
Mariana Landín ◽  
Pedro Pablo Gallego
2013 ◽  
Vol 59 (6) ◽  
pp. 622-635 ◽  
Author(s):  
I.V. Fedyushkina ◽  
V.S. Skvortsov ◽  
I.V. Romero Reyes ◽  
I.S. Levina

A series of 42 steroid ligands was used to predict a binding affinity to progesterone receptor. The molecules were the derivatives of 16a,17a-cycloalkanoprogesterones. Different methods of prediction were used and analyzed such as CoMFA and artificial neural networks. The best result (Q2=0.91) was obtained for a combination of molecular docking, molecular dynamics simulation and artificial neural networks. A predictive power of the model was validated by a group of 8 pentarans synthesized separately and tested in vitro (R2test=0.77). This model can be used to determine the affinity level of the ligand to progesterone receptor and accurate ranking of binding compounds.


1993 ◽  
Vol 39 (11) ◽  
pp. 2248-2253 ◽  
Author(s):  
P K Sharpe ◽  
H E Solberg ◽  
K Rootwelt ◽  
M Yearworth

Abstract We studied the potential benefit of using artificial neural networks (ANNs) for the diagnosis of thyroid function. We examined two types of ANN architecture and assessed their robustness in the face of diagnostic noise. The thyroid function data we used had previously been studied by multivariate statistical methods and a variety of pattern-recognition techniques. The total data set comprised 392 cases that had been classified according to both thyroid function and 19 clinical categories. All cases had a complete set of results of six laboratory tests (total thyroxine, free thyroxine, triiodothyronine, triiodothyronine uptake test, thyrotropin, and thyroxine-binding globulin). This data set was divided into subsets used for training the networks and for testing their performance; the test subsets contained various proportions of cases with diagnostic noise to mimic real-life diagnostic situations. The networks studied were a multilayer perceptron trained by back-propagation, and a learning vector quantization network. The training data subsets were selected according to two strategies: either training data based on cases with extreme values for the laboratory tests with randomly selected nonextreme cases added, or training cases from very pure functional groups. Both network architectures were efficient irrespective of the type of training data. The correct allocation of cases in test data subsets was 96.4-99.7% when extreme values were used for training and 92.7-98.8% when only pure cases were used.


DYNA ◽  
2020 ◽  
Vol 87 (212) ◽  
pp. 244-250
Author(s):  
Luz América Espinosa-Sandoval ◽  
Claudia Isabel Ochoa-Martínez ◽  
Alfredo Adolfo Ayala-Aponte

In Vitro Release modeling (IVR) of nanoencapsulated phenolic compounds (PC) is complex, due to the number of factors involved in the process. Artificial Neural Networks (ANN) are useful tools for its prediction because they consider the effect of all factors on the response. The release at 5h is crucial in kinetics because, in most cases, it is an equilibrium point leading to a constant phase. The objective of this investigation was to predict the IVR of nanoencapsulated PC at 5h using ANN. A database with information from the scientific literature was used. This model permits mathematical correlation of the IVR at 5h with eleven factors. The optimal network configuration consisted of one hidden layer with one neuron. A mathematical model was obtained with a Mean Square Error (MSE) of 0.0516 and a correlation coefficient (r) of 0.8413.


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