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Approaches for Integration of multiple ‘Omic’
Data
Dmitry Grapov, PhD
Examples
Nature Reviews Genetics 15, 107–120 (2014) doi:10.1038/nrg3643
FBA = flux-balance analysis
• Topological enrichment can give broad overview
of impacted genes, proteins and metabolites
• Changes in biochemical domains corroborated
by multi-Omic data sets can be used to identify
robust candidates responsible for phenotypic
variation between comparisons
• Gene-gene, protein-protein or gene-protein
interaction networks can be used to
deconvolute ambiguous metabolic pathways
Common Approaches
Nature Reviews Genetics 15, 107–120 (2014) doi:10.1038/nrg3643
Biochemical Domain
Enrichment Analysis
• Genes/Proteins  DAVID, AmiGo, etc GO:terms
• Genes/Proteins + Metabolites  IMPaLA: Integrated Molecular
Pathway Level Analysis (http://impala.molgen.mpg.de/)  pathways
1. Classify all species domains (e.g. biological process, pathway, etc)
2. Calculate probability of observing changes in species by chance
IMPaLA: Gene + Metabolite
pathway enrichment
Challenges:
•Removal of redundant information
•Preference of specific vs. generic pathways
•Visualization of gene + metabolite + pathway relationships
Determining significance of the
enrichment: Hypergeometric Test
How to calculate statistics to determine enrichment?
hit.num = 51 # number of significantly changed pathway
metabolites
set.num = 1455 # number of metabolites in pathway
full = 3358 # all possible metabolites in organism
q.size = 72 # number of significantly changed metabolites
phyper(hit.num-1, set.num, full-set.num, q.size, lower.tail=F)
= 1.717553e-06
GO Enrichment analysis:
Hierarchy of Redundancy (parents)
• GO is an ontology wherein enrichment is often
shared by children and parents.
• Difficult to co-visualize term hierarchy and gene to
term mapping
Enrichment networks:
Removing the Hierarchy of
Redundancy
Workflow:
1. If two nodes share all genes, drop least
enriched (highest p-value)
2. Filter terms based on enrichment
3. Display term to gene/protein
relationships as edges in a network
4. Map direction of change in
genes/proteins to network node
attributes
Enrichment Network
Mapping of parents through children
GO enrichment network displays:
• gene names associated with
each overrepresented term
• Fold change in protein
expression between two
groups (can be extended k>2
groups)
• Can display enrichment p-
value for each term
• Can incorporate metabolites
as children of genes
Empirical Networks
• Correlation based networks (CN)
(simple, tendency to hairball)
• GGM or partial correlation based
networks (advanced, preference
of direct over indirect
relationships
• *Increase in robustness with
sample size
10.1007/978-1-4614-1689-0_17
Topological
Enrichment
Networks
http://pubchem.ncbi.nlm.nih.gov//score_matrix/score_matrix.cgi
http://www.genome.jp/dbget-bin/www_bget?rn:R00975
gene gene
Topological Enrichment Networks:
genes + proteins + metabolites
metabolite
metabolite
protein
gene
MetaMapR
Biological network generator
https://github.com/dgrapov/MetaMapR
dgrapov@ucdavis.edu
metabolomics.ucdavis.edu
This research was supported in part by NIH 1 U24 DK097154

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Omic Data Integration Strategies

  • 1. Approaches for Integration of multiple ‘Omic’ Data Dmitry Grapov, PhD
  • 2. Examples Nature Reviews Genetics 15, 107–120 (2014) doi:10.1038/nrg3643 FBA = flux-balance analysis • Topological enrichment can give broad overview of impacted genes, proteins and metabolites • Changes in biochemical domains corroborated by multi-Omic data sets can be used to identify robust candidates responsible for phenotypic variation between comparisons • Gene-gene, protein-protein or gene-protein interaction networks can be used to deconvolute ambiguous metabolic pathways
  • 3. Common Approaches Nature Reviews Genetics 15, 107–120 (2014) doi:10.1038/nrg3643
  • 4. Biochemical Domain Enrichment Analysis • Genes/Proteins  DAVID, AmiGo, etc GO:terms • Genes/Proteins + Metabolites  IMPaLA: Integrated Molecular Pathway Level Analysis (http://impala.molgen.mpg.de/)  pathways 1. Classify all species domains (e.g. biological process, pathway, etc) 2. Calculate probability of observing changes in species by chance
  • 5. IMPaLA: Gene + Metabolite pathway enrichment Challenges: •Removal of redundant information •Preference of specific vs. generic pathways •Visualization of gene + metabolite + pathway relationships
  • 6. Determining significance of the enrichment: Hypergeometric Test How to calculate statistics to determine enrichment? hit.num = 51 # number of significantly changed pathway metabolites set.num = 1455 # number of metabolites in pathway full = 3358 # all possible metabolites in organism q.size = 72 # number of significantly changed metabolites phyper(hit.num-1, set.num, full-set.num, q.size, lower.tail=F) = 1.717553e-06
  • 7. GO Enrichment analysis: Hierarchy of Redundancy (parents) • GO is an ontology wherein enrichment is often shared by children and parents. • Difficult to co-visualize term hierarchy and gene to term mapping
  • 8. Enrichment networks: Removing the Hierarchy of Redundancy Workflow: 1. If two nodes share all genes, drop least enriched (highest p-value) 2. Filter terms based on enrichment 3. Display term to gene/protein relationships as edges in a network 4. Map direction of change in genes/proteins to network node attributes
  • 9. Enrichment Network Mapping of parents through children GO enrichment network displays: • gene names associated with each overrepresented term • Fold change in protein expression between two groups (can be extended k>2 groups) • Can display enrichment p- value for each term • Can incorporate metabolites as children of genes
  • 10. Empirical Networks • Correlation based networks (CN) (simple, tendency to hairball) • GGM or partial correlation based networks (advanced, preference of direct over indirect relationships • *Increase in robustness with sample size 10.1007/978-1-4614-1689-0_17
  • 12. gene gene Topological Enrichment Networks: genes + proteins + metabolites metabolite metabolite protein gene
  • 14. dgrapov@ucdavis.edu metabolomics.ucdavis.edu This research was supported in part by NIH 1 U24 DK097154