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. 2018 Jun 19;5:180117. doi: 10.1038/sdata.2018.117

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Copyright © 2018, The Author(s)

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

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LINCS Assays are classified according to a generic subject area (a: transcriptomics, b: proteomics, c: epigenomics, d: binding, e: imaging). For each assay, the number of unique perturbations, model systems, datasets, profiles (signatures) and the DSGC is annotated. Only assays used by DSGCs of LINCS Phase 2 are shown. Perturbations include small molecules, genetic antibodies, and other ligands. Model systems include cell lines, primary cells, differentiated cells, iPSCs and Embryonic Stem Cells. b: BroadT LINCS, P: PCCSE, N: NeuroLINCS, H: HMS LINCS, D: DtoxS, M: MEP LINCS, D.B.: Disease Background, F.I.: Fluorescence Imaging.