Graph isomorphism‑based algorithm for cross‑checking chemical and crystallographic descriptions Merkys, Andrius Quirós Olozábal, Miguel Molecular graphs Graph isomorphism SMILES Crystallography Open Database Published reports of chemical compounds often contain multiple machine-readable descriptions which may supplement each other in order to yield coherent and complete chemical representations. This publication presents a method to cross-check such descriptions using a canonical representation and isomorphism of molecular graphs. If immediate agreement between compound descriptions is not found, the algorithm derives the minimal set of simplifications required for both descriptions to arrive to a matching form (if any). The proposed algorithm is used to cross-check chemical descriptions from the Crystallography Open Database to identify coherently described entries as well as those requiring further curation. 2023-03-29T09:32:01Z 2023-03-29T09:32:01Z 2023-02-23 journal article Merkys, A... [et al.]. Graph isomorphism-based algorithm for cross-checking chemical and crystallographic descriptions. J Cheminform 15, 25 (2023). [https://doi.org/10.1186/s13321-023-00692-1] https://hdl.handle.net/10481/80924 10.1186/s13321-023-00692-1 eng http://creativecommons.org/licenses/by/4.0/ open access Atribución 4.0 Internacional BMC