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We open the web laboratory and load its built-in example. This
walkthrough uses real application screenshots

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with synthetic data. It does not demonstrate an experimental
Bruker import.

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The example contains twenty-four gradients and four signals.
Before interpreting results, check the displayed

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context and selected resonance. These demonstration values are
not measurements from a real sample.

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The expanded view lets you compare signals and indicative
molecular regions. Inspect the overlaid traces and

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markers before selecting a peak. These regions guide exploration
without confirming molecular identities.

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The screenshot follows a click near seven point two five parts
per million. The marker identifies the original

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local maximum. Its panel brings together the position, candidates
and results from the example.

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Rectangle mode lets you drag an area to zoom into the peak. This
screenshot shows the result of that real

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gesture. Changing the view does not alter intensities or select
different scientific observations.

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The reference panel shows candidates, companion positions and
sources. Those literature positions are not

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observed detections of companion signals. Review context and
evidence before assigning an identity, and save

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your decisions with the project.