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Frontal alpha asymmetry increased observed BDI prediction error in a fixed ridge test across two rest runs from 114 adults in OpenNeuro ds003478 v1.1.0

We tested whether frontal alpha asymmetry improves prediction of Beck Depression Inventory (BDI) scores. We used OpenNeuro ds003478 version 1.1.0. Fixed rules retained 114 adults. For each test person, we trained on the first rest run from the other 113 people. We tested on the second run from that person. The base ridge model used age, sex, and mean F3/F4 log alpha power. The added model also used F4 minus F3 log alpha power. We fixed the penalty before score analysis. Root mean squared error rose from 10.715 to 10.886 BDI points after asymmetry was added. Base minus added mean squared error was -3.694 squared BDI points. A 5,000-draw person bootstrap refit interval was [-15.143, 0.418]. The interval includes zero. All seven planned model checks also had negative observed gains. The result concerns these features, this fixed model, and this selected young sample. Population and clinical use require separate tests. The package preserves code, 243 source-linked feature records, individual predictions, all bootstrap draws, and reproduction instructions. Two new full raw record replays, all input hashes, an independent solver, and a complete repeated analysis passed.

frontal alpha asymmetry · EEG · BDI · ridge regression · person-held-out prediction · OpenNeuro ds003478

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References

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  1. usesFixed sample rules and a 150-unit screen retained 6 of 122 public adults with 60 accepted closed-eye seconds in each rest run in OpenNeuro ds003478 v1.1.0 sci:sha256:3d4bee314ed5e3e9366fa0902e57d18d5367a1204cb7ca5cb4334ddfad95f62e

    We used its exact alpha window features, source tables, raw file hashes, and extractor. We added a person-held-out test of BDI prediction across two rest runs.

  2. usesdoi:10.18112/openneuro.ds003478.v1.1.0

    The analysis used ds003478 v1.1.0 features and source records; two raw records were replayed against release hashes.

  3. doi:10.1016/j.nicl.2017.07.006
  4. doi:10.3390/biomedicines12092054

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