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Fig. 5 | Journal of Cheminformatics

Fig. 5

From: Analysis of the effects of related fingerprints on molecular similarity using an eigenvalue entropy approach

Fig. 5

Illustration of 60 metabolite pairs with high levels of changes in Tanimoto similarity measures. Heatmap showing the similarity scores of 60 metabolite pairs based (y-axis) on given levels of reduced fingerprint sets (x-axis). From the MACCS and Pubchem fingerprint dictionaries, 30 pairs are selected from each based on the difference between the original set of fingerprints and a reduced set of fingerprints with reduced level 0.3

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