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Related Concept Videos

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Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
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Genetic polymorphism in drug metabolism is crucial to the inter-individual variability observed in drug responses. Drug metabolism primarily involves the chemical modification of drugs and other xenobiotics to enhance their elimination by increasing their polarity. Two main classes of enzymes mediate this biotransformation process: Phase I enzymes, primarily cytochrome P450s, catalyze oxidation and reduction reactions, while other enzymes, such as esterases, mediate hydrolysis, and Phase II...
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Related Experiment Video

Updated: May 13, 2026

Large Scale Non-targeted Metabolomic Profiling of Serum by Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS)
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Published on: March 14, 2013

Leveraging non-targeted metabolite profiling via statistical genomics.

Miaoqing Shen1, Corey D Broeckling, Elly Yiyi Chu

  • 1Boyce Thompson Institute for Plant Research, Ithaca, New York, United States of America.

Plos One
|March 8, 2013
PubMed
Summary

Systems biology integrates diverse data for a holistic view. This study uses network analysis of maize kernel metabolomics and genomics to reveal genetic control of biochemical networks, enhancing biological interpretation.

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Area of Science:

  • Systems biology
  • Metabolomics
  • Genomics
  • Bioinformatics

Background:

  • Integrating multi-omics data is a key challenge in systems biology.
  • Maize kernels are a model system for genomic studies and crucial for the agroeconomy.

Purpose of the Study:

  • To develop a network analysis framework for integrating maize kernel metabolomics data.
  • To identify genetic control of biochemical networks through genome-wide association studies.

Main Methods:

  • Mass spectrometry-based profiling of maize kernels from 210 varieties.
  • Network analysis to organize detected features into distinct modules.
  • Calculation of module eigenvalues for genome-wide association studies.

Main Results:

  • A single network framework incorporated 97.5% of detected features.
  • 47.1% of compounds organized into 48 distinct network modules.
  • Nineteen modules showed significant associations, indicating genetic control of biochemical networks.

Conclusions:

  • Leveraging genome-metabolome correlations enhances annotation and biological interpretation.
  • The developed method is applicable to other organisms with adequate bioinformatic resources.
  • This approach provides insights into the genetic architecture of maize kernel biochemistry.