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