A Computer Program for Classifying Plants.
By D. Rogers, T. T. Tanimoto. 1960
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- Paul D. Adams
- Pavel V. Afonine
- Nigel W. Moriarty
- Chengxin Zhang
- Nathaniel Echols
- T. C. Terwilliger
- Yang Zhang
- Ryan G. Coleman
Citations in the corpus
- Efficient searching and annotation of metabolic networks using chemical similarity (2015, methodology): “S1) fingerprint similarity measured using the Tanimoto coefficient (Rogers and Tanimoto, 1960) (s) to guide the network search, making the use of traditional pathway search algorithms a more tractable undertaking.”
- Structure and dynamics of molecular networks: A novel paradigm of drug discovery: A comprehensive review (2012, background): “…numerical descriptions of similarity listed in Table 5,wewillfirst consider those networks, which are based on simple chemical similarity of the compounds involved using e.g. the Tanimoto-coefficient for the definition of edges (Rogers & Tanimoto, 1960; Tanaka et al., 2009; Bickerton et al., 2012).”
- Nearest-Neighbor Searching and Metric Space Dimensions (2005, background): “The special case for finite sets |A∆B|/|A ∪ B| is called the Tanimoto distance [RT60], resemblance [Bro97], set similarity distance [Cha02], Jaccard distance [Jac01, Spa80], or Marczewski-Steinhaus distance [MS58].”
- BRENDA in 2019: a European ELIXIR core data resource (2018, methodology): “In the similarity search only the fingerprint scan is carried out taking into account the Tanimoto coefficient (26) - a measure for similarity - and the previously user-defined minimal similarity as lower boundary.”
- The incorporation of protein flexibility and conformational energy penalties in docking screens to improve ligand discovery (2014, background): “The new hits differed from previously known ligands: the highest pairwise topological similarity to these, using ECFP4-based Tanimoto 47 coefficients, was 0.36 (Suppl.”
- COFACTOR: improved protein function prediction by combining structure, sequence and protein–protein interaction information (2017, methodology): “Different ligands within the same binding pocket are further grouped by the average linkage clustering with chemical similarity, using the Tanimoto coefficient (22) with a cut-off of 0.”
- Cryptanalysis of Basic Bloom Filters Used for Privacy Preserving Record Linkage (2014, methodology): “For example, the British Office for National Statistics considered several methods for linking administrative data within the Beyond 2011 Programme, but refrained from all “(. . . ) recent innovations, such as bloom filter encryption (. . . )” since they “(. . . ) have not been fully explored from a”
- Ligand placement based on prior structures: the guided ligand-replacement method (2013, methodology): “The Tanimoto coefficient (Rogers & Tanimoto, 1960) is one way to quantify the similarity between two fingerprints [0 (no compared features match) Tanimoto coefficient 1 (all compared features match)].”
- A model for spectra-based software diagnosis (2011, background): “Botany has also spawned several other metrics: Ochiai [1957], Russell and Rao [1940], Sorensen and Dice [Dice 1945; Duarte et al. 1999], Rogers and Tanimoto [1960] , Anderberg [1973] and Simple-Matching [Meyer et al. 2004].”