Quality Assessment Methods

Our platform employs several industry-standard and custom algorithms to ensure the integrity of your metabolomics data.

๐Ÿ“Š Statistical Analysis & Outlier Detection
Uses Z-score based calculations to identify metabolites that deviate significantly from the mean. This method is crucial for detecting sample preparation errors or biological anomalies.
Mean Std Dev Z-score IQR
๐Ÿ‘ฏ Identical Concentrations Check
Flags metabolites that show identical concentration values across multiple samples. While rare in biology, this often indicates technical replicas, data entry errors, or sensor saturation issues.
Value Matching Cross-Sample Variance
๐Ÿ”ฌ LOD (Limit of Detection) Analysis
Evaluates data against the Limit of Detection (LOD). High percentages of values below LOD can skew statistical results and may require imputation or exclusion from certain downstream analyses.
LOD % LOD Outliers
๐ŸŒ HMDB Range Validation
Compares observed concentrations against physiologically expected ranges documented in the Human Metabolome Database (HMDB). Values outside these ranges are flagged for review.
Reference Ranges Physiological Limits
๐Ÿงช Urine Normalization
Adjusts metabolite concentrations based on Creatinine levels or other normalization factors. This accounting for hydration levels is essential for accurate comparative analysis of urine samples.
Creatinine Normalization Dual-Run Analysis

Need More Help?

If you're unsure which methods to select for your dataset, we recommend using the "Select All" option during upload for a comprehensive assessment.

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