{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T04:55:43Z","timestamp":1790744143000,"version":"4.1.0"},"reference-count":54,"publisher":"Oxford University Press (OUP)","issue":"9","license":[{"start":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T00:00:00Z","timestamp":1788825600000},"content-version":"vor","delay-in-days":7,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"European Union\u2019s Horizon Europe Partnership for the Assessment of Risks for Chemicals","award":["101057014"],"award-info":[{"award-number":["101057014"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,9,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Omics technologies are increasingly integrated into next-generation risk assessment, yet quantitative toxicogenomics outcomes remain highly dependent on analytical choices, motivating a systematic evaluation of how bioinformatics workflows influence hazard characterization and transcriptomic Points of Departure (tPOD). Here, we applied 5 independent transcriptomics pipelines to a shared dataset of RPTEC\/TERT1 kidney cells exposed to cisplatin across multiple concentrations and time points, comparing effects of pre-processing, benchmark concentration modeling, and pathway-based interpretation strategies. Across workflows, substantial variability was observed in gene-level benchmark concentrations (BMCs). This variability was associated with differences in normalization, filtering, and modeling software, although the present design does not isolate the contribution of individual workflow choices. Despite this variability, convergence increased at later time points as transcriptional responses strengthened, with 24\u2009h consistently identified as the most sensitive time point at the gene level. Aggregation of gene-level BMCs into pathway-based metrics reduced variability but did not eliminate it, with pathway definition emerging as a major determinant of tPOD estimates. Notably, distinct pathway resources showed minimal gene overlap, and smaller, biologically coherent gene sets (e.g. co-expression modules and biomarker panels) produced lower and less dispersed BMCs compared with broader pathway annotations. Furthermore, direct modeling of pathway activity scores yielded systematically different tPODs relative to median-based aggregation, with method-dependent conservativeness influenced by pathway coverage and response strength. Overall, our findings demonstrate that both analytical workflow design and pathway selection critically shape toxicogenomic-derived potency estimates, highlighting the need for harmonized, transparent methodologies to enable robust application of transcriptomics in chemical safety assessment and regulatory decision-making.<\/jats:p>","DOI":"10.1093\/toxsci\/kfag115","type":"journal-article","created":{"date-parts":[[2026,9,4]],"date-time":"2026-09-04T11:40:12Z","timestamp":1788522012000},"source":"Crossref","is-referenced-by-count":0,"title":["Analytical choices drive toxicogenomic potency estimates: a systematic evaluation of transcriptomic points of departure"],"prefix":"10.1093","volume":"209","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-9681-6693","authenticated-orcid":false,"given":"Imke B","family":"Bruns","sequence":"first","affiliation":[{"name":"Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research, Leiden University , Leiden, 2333 CC,","place":["the Netherlands"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dayna R","family":"Schultz","sequence":"additional","affiliation":[{"name":"Environmental Engineering Laboratory, Department of Chemical Engineering, Aristotle University of Thessaloniki , Thessaloniki, 54124,","place":["Greece"]},{"name":"HERACLES Research Center on the Exposome and Health, Center for Interdisciplinary Research and Innovation , Balkan Center, Bldg. 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B, Thessaloniki, 57001,","place":["Greece"]},{"name":"National Hellenic Research Foundation , Athens, 11635,","place":["Greece"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elisavet","family":"Renieri","sequence":"additional","affiliation":[{"name":"Environmental Engineering Laboratory, Department of Chemical Engineering, Aristotle University of Thessaloniki , Thessaloniki, 54124,","place":["Greece"]},{"name":"HERACLES Research Center on the Exposome and Health, Center for Interdisciplinary Research and Innovation , Balkan Center, Bldg. 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