sep-l1000

is a Data Source.

SEP-L1000 (Side Effect Prediction based on L1000 data) is a web portal from the Ma'ayan Laboratory that presents adverse drug reaction (ADR) predictions for 20,412 small molecules profiled by the LINCS L1000 project across 1,054 side effects. Predictions come from multi-label extremely randomized trees classifiers trained on known ADRs from SIDER and OFFSIDES, using L1000 gene expression signatures, Gene Ontology enrichment vectors, chemical fingerprints, and cell morphology profiles as features. The processed feature and label matrices are available for download.

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Homepage

sep-l1000

Repository

GitHub

External IDs

No external IDs available

Product Summary

Products

From this Resource
ID Name URL Category Format Description
sep-l1000.portal SEP-L1000 Web Portal SEP-L1000 Graphical Interface http Web portal for browsing and searching...
sep-l1000.faers-offsides SEP-L1000 FAERS OFFSIDES Side Effect Matrix FAERS_offsides_PTs.csv.gz (452.2 KB) Product csv Off-label drug-ADR matrix (684 drugs ...
sep-l1000.sider SEP-L1000 SIDER Side Effect Matrix SIDER_PTs.csv.gz (165.9 KB) Product csv On-label drug-ADR matrix (834 drugs b...
sep-l1000.lincs-signatures SEP-L1000 LINCS L1000 CD Signatures LINCS_Gene_Experssion_signatures_CD.csv.gz (38.6 MB) Product csv Characteristic direction gene express...
sep-l1000.go-signatures SEP-L1000 GO-Transformed Signatures GO_transformed_signatures_PAEA.csv.gz (219.9 MB) Product csv Gene Ontology transformed L1000 signa...
sep-l1000.maccs-fingerprints SEP-L1000 MACCS Fingerprints MACCS_bitmatrix.csv.gz (1.2 MB) Product csv 166-bit MACCS chemical fingerprint ma...
sep-l1000.mlpcn-morphology SEP-L1000 MLPCN Morphological Profiles MLPCN_morplological_profiles.csv.gz (52.9 MB) Product csv Cell morphology profiles (812 Cell Pa...
sep-l1000.strongest-signatures-metadata SEP-L1000 Strongest Signature Metadata meta_LINCS_strongest_signatures.csv (31.8 MB) Product csv Metadata mapping each LINCS L1000 com...
sep-l1000.probes-metadata SEP-L1000 Probe Metadata meta_Probes_info.csv (361.7 KB) Product csv Mapping of L1000 probes to gene symbols.
sep-l1000.smiles-metadata SEP-L1000 Compound SMILES Metadata meta_SMILES.csv (3.8 MB) Product csv Compound metadata for 41,774 LINCS L1...
From other Resources
ID Name URL Category Format Relation Description
drugmonizome.libraries ⚠ Drugmonizome Drug Set Libraries libraries Product json was derived from The 35 Drugmonizome drug set librarie...

Details

SEP-L1000

SEP-L1000 is a web portal from the Ma’ayan Laboratory at the Icahn School of Medicine at Mount Sinai that prioritizes adverse drug reactions (ADRs) for approved drugs and preclinical small molecules. It was built with support from the BD2K-LINCS Data Coordination and Integration Center and the NIH Illuminating the Druggable Genome program, and accompanies Wang, Clark and Ma’ayan 2016 (Bioinformatics).

Data Content

Known on-label ADRs come from SIDER and off-label ADRs from OFFSIDES (processed FAERS reports), with ADR terms mapped to MedDRA preferred terms. Features for each compound include characteristic direction signatures from the strongest LINCS L1000 experiment, Gene Ontology enrichment vectors derived from those signatures, MACCS and PubChem chemical fingerprints, and cell morphology profiles from the Broad Institute MLPCN profiling dataset. DrugBank names and synonyms were used to map marketed drugs to L1000 compounds. Extremely randomized trees classifiers, one per ADR, were applied to all profiled compounds; the portal reports predictions for 20,412 compounds and 1,054 side effects.

Access

The portal lets users browse drugs and side effects, search, and view side effect-GO term and side effect-phenotype networks. The download page provides the processed side effect matrices, signature and fingerprint matrices, morphology profiles, and metadata as CSV files. The site is served over HTTP only; the HTTPS address does not respond. It was online and its database backend was answering queries on 2026-10-19.

License

No license is stated on the site or in the GitHub repository. Users are asked to cite Wang et al. 2016.

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Created: October 19, 2026 | Last modified: October 19, 2026