Cargando…
jCompoundMapper: An open source Java library and command-line tool for chemical fingerprints
BACKGROUND: The decomposition of a chemical graph is a convenient approach to encode information of the corresponding organic compound. While several commercial toolkits exist to encode molecules as so-called fingerprints, only a few open source implementations are available. The aim of this work is...
Autores principales: | Hinselmann, Georg, Rosenbaum, Lars, Jahn, Andreas, Fechner, Nikolas, Zell, Andreas |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033338/ https://www.ncbi.nlm.nih.gov/pubmed/21219648 http://dx.doi.org/10.1186/1758-2946-3-3 |
Ejemplares similares
-
Estimation of the applicability domain of kernel-based machine learning models for virtual screening
por: Fechner, Nikolas, et al.
Publicado: (2010) -
Optimal assignment methods for ligand-based virtual screening
por: Jahn, Andreas, et al.
Publicado: (2009) -
Efficient extraction of canonical spatial relationships using a recursive enumeration of k-subsets
por: Hinselmann, Georg, et al.
Publicado: (2010) -
Automatic pharmacophore model generation using weighted substructure assignments
por: Jahn, Andreas, et al.
Publicado: (2010) -
Kernel-based estimation of the applicability domain of QSAR models
por: Fechner, Nikolas, et al.
Publicado: (2010)