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Targeted Metabolomics MRM & PRM Quantification Training | Panel Design, Calibration & Validation

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Metabolomics, Lipidomics & Small-Molecule Omics >> Targeted Metabolomics MRM & PRM Quantification Training | Panel Design, Calibration & Validation

Targeted Metabolomics MRM & PRM Quantification — Hands-on

Build robust targeted metabolomics assays using MRM and PRM. You will work through panel design, transition selection, internal standard strategies, calibration curves, validation parameters and reporting so that your targeted methods are ready for translational, preclinical or QC contexts.

Targeted Metabolomics MRM & PRM Quantification
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Session 1
Fee: Rs 8800
Targeted Metabolomics Concepts & Panel Design
  • When and why to use targeted metabolomics
  • hypothesis driven questions clinical and preclinical studies method translation from discovery
  • Panel design and metabolite selection
  • pathway centric panels disease or toxicity markers coverage versus runtime trade offs
  • Standards, reference materials and documentation
  • neat standards and mixes reference matrices panel specification sheets
Session 2
Fee: Rs 11800
MRM & PRM Method Development
  • Transition selection and optimization
  • precursor ion choice product ion selection collision energy optimization
  • Scheduling and dwell time strategies
  • scheduled MRM windows cycle time targets balancing sensitivity and coverage
  • Chromatographic and source conditions for robust quant
  • coelution checks matrix and ion suppression awareness system suitability for targeted runs
Session 3
Fee: Rs 14800
Calibration, Internal Standards & Quant Workflows
  • Internal standard strategies
  • isotopically labeled standards class specific standards spiking and recovery checks
  • Calibration curve construction and fitting
  • concentration ranges weighting schemes back calculation and residuals
  • Quantitation workflows and batch calculations
  • using curve fits for unknowns handling dilution factors preparing analysis ready concentration tables
Session 4
Fee: Rs 18800
Validation, QC Metrics & Reporting
  • Method validation parameters and acceptance criteria
  • accuracy and precision LOD LOQ and linearity carryover and stability checks
  • Run level QC monitoring and flags
  • QC samples and control charts fail criteria and repeats batch acceptance decisions
  • Reporting concentrations and documenting methods
  • summary tables by analyte plots for stakeholders method and validation reports


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