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In biology, determination is the process of matching a specimen or sample of an organism to a known taxon, for example identifying a plant as belonging to a particular species. Expert taxonomists may perform this task, but structures created by taxonomists are sometimes used by non-specialists.
In computer vision, 3D object recognition involves recognizing and determining 3D information, such as the pose, volume, or shape, of user-chosen 3D objects in a photograph or range scan. Typically, an example of the object to be recognized is presented to a vision system in a controlled environment, and then for an arbitrary input such as a ...
The database of three-dimensional interacting domains (3did) is a biological database containing a catalogue of protein-protein interactions for which a high-resolution 3D structure is known.
Homology model of the DHRS7B protein created with Swiss-model and rendered with PyMOL. Homology modeling, also known as comparative modeling of protein, refers to constructing an atomic-resolution model of the "target" protein from its amino acid sequence and an experimental three-dimensional structure of a related homologous protein (the "template").
The automated identification of biological objects such as insects (individuals) and/or groups (e.g., species, guilds, characters) has been a dream among systematists for centuries. The goal of some of the first multivariate biometric methods was to address the perennial problem of group discrimination and inter-group characterization.
UCSF Chimera (or simply Chimera) is an extensible program for interactive visualization and analysis of molecular structures and related data, including density maps, supramolecular assemblies, sequence alignments, docking results, trajectories, and conformational ensembles. [1]
Identifying moths. Identification in biology is the process of assigning a pre-existing taxon name to an individual organism.Identification of organisms to individual scientific names (or codes) may be based on individualistic natural body features, [1] experimentally created individual markers (e.g., color dot patterns), or natural individualistic molecular markers (similar to those used in ...
It offers a solution to map NGS short reads with a moderate distance (up to 30% sequence divergence) from reference genomes. It poses no restrictions on the size of the reference, which, combined with its high sensitivity, makes the Variant Toolkit well-suited for targeted sequencing projects and diagnostics.