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        <datestamp>2026-10-02T11:18:07Z</datestamp>
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          <dc:title>Validation Strategy Dominates Model Choice in Chronological
QSAR Evaluation</dc:title>
          <dc:creator>Filipa Almendra (25301940)</dc:creator>
          <dc:creator>Andre O. Falcao (1773145)</dc:creator>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Information Systems not elsewhere classified</dc:subject>
          <dc:subject>Mathematical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Marine Biology</dc:subject>
          <dc:subject>Inorganic Chemistry</dc:subject>
          <dc:subject>Science Policy</dc:subject>
          <dc:subject>Plant Biology</dc:subject>
          <dc:subject>binary classification tasks</dc:subject>
          <dc:subject>48 without changing</dc:subject>
          <dc:subject>set composition could</dc:subject>
          <dc:subject>mean mcc values</dc:subject>
          <dc:subject>five validation conditions</dc:subject>
          <dc:subject>support vector machine</dc:subject>
          <dc:subject>mean cv mcc</dc:subject>
          <dc:subject>estimated qsar generalization</dc:subject>
          <dc:subject>chronological validation produced</dc:subject>
          <dc:subject>chronological validation penalty</dc:subject>
          <dc:subject>chronological validation set</dc:subject>
          <dc:subject>random validation set</dc:subject>
          <dc:subject>chronological validation</dc:subject>
          <dc:subject>set definition</dc:subject>
          <dc:subject>validation mcc</dc:subject>
          <dc:subject>cv estimate</dc:subject>
          <dc:subject>validation compounds</dc:subject>
          <dc:subject>test splits</dc:subject>
          <dc:subject>temporally close</dc:subject>
          <dc:subject>structural redundancy</dc:subject>
          <dc:subject>structural filtering</dc:subject>
          <dc:subject>selection workflow</dc:subject>
          <dc:subject>results indicate</dc:subject>
          <dc:subject>primarily explained</dc:subject>
          <dc:subject>external estimates</dc:subject>
          <dc:subject>examined whether</dc:subject>
          <dc:subject>dominant influence</dc:subject>
          <dc:description>Quantitative structure–activity
relationship (QSAR) models
are commonly evaluated by random cross-validation or random train-test
splits, but these retrospective procedures may overestimate performance
when validation compounds are structurally or temporally close to
the training data. In this study, we examined whether this optimism
is primarily explained by structural redundancy, chronological data
set evolution, or the choice of machine-learning model. Fourteen public
ChEMBL bioactivity data sets were curated as binary classification
tasks. Five validation conditions were compared: random validation,
chronological validation by publication year, a size-matched randomly
thinned control, structural filtering of the random validation set,
and structural filtering of the chronological validation set. Model
development was deliberately held fixed within the random-derived
and year-derived comparisons, so that the effect of validation-set
composition could be assessed without simultaneously changing the
training cohort. Four standard QSAR model classesrandom forest,
support vector machine, XGBoost, and a feed-forward neural networkwere
evaluated under the same training-only model-selection workflow. Random
validation produced closely aligned internal and external estimates,
with mean MCC values of 0.75 and 0.72, respectively, while random
thinning gave essentially unchanged validation performance (MCC 0.73).
Structural filtering reduced validation MCC to 0.48 without changing
the corresponding training-only CV estimate. Chronological validation
produced a much larger generalization gap, with mean CV MCC of 0.73
and validation MCC of 0.19; additional structural filtering reduced
validation MCC to 0.15. Model-class comparisons showed substantial
overlap among classifiers, and no standard algorithm consistently
overcame the chronological validation penalty. These results indicate
that validation-set definition has a dominant influence on estimated
QSAR generalization and that chronological data set shift is not reproduced
by random or structure-only validation.</dc:description>
          <dc:date>2026-10-02T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acs.jcim.6c02796.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Validation_Strategy_Dominates_Model_Choice_in_Chronological_QSAR_Evaluation/34056294</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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