Hi everyone,
I am a PhD student at UNSW currently working with LC–MS metabolomics data. I have been struggling to process my peak intensity table in MetaboAnalyst, as my dataset consistently fails the integrity check.
My dataset includes:
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5 pooled quality control (QC) samples
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P. aeruginosa treated under the following conditions:
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Drug A (1 hr, 3 hr)
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Drug B (1 hr, 3 hr)
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Combination of Drug A and Drug B (1 hr, 3 hr)
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Each condition contains six biological replicates
I would greatly appreciate any guidance on how to properly format and structure my data table so that it passes the integrity check in MetaboAnalyst. Additionally, I would be very grateful for recommendations on appropriate data filtering and normalization settings for this type of dataset.
Thank you very much for your help!