OICR Cancer Stem Cell program - Pathway and Network Analysis Service
The Pathway and Network Analysis Service is freely available to all Cancer Stem Cell program members.
High-throughput genomic experiments (e.g. gene expression, large-scale genetic screens) often lead to the identification of large gene lists. The interpretation of results and the formulation of consistent biological hypotheses from these gene lists can be challenging. Pathway and network analysis (e.g enrichment analysis) approaches can aid interpretation by relating the gene list to knowledge about the biological system, such as pathways.
Our goal is to help researchers interpret results of genomics experiments. Analysis is conducted in close collaboration with researchers on each project to ensure correct input data and effective interpretation of results. Ideally researchers do as much of the analysis and interpretation as they can.
Standard types of pathway analysis offered
Pathway and network analysis: find pathways enriched in a list of genes (e.g. differentially expressed genes)
Gene-set enrichment analysis helps characterize large gene lists by finding functionally coherent gene-sets, such as pathways, that are statistically over-represented in a given gene list. We have also developed a method to visualize the results of this analysis, called Enrichment Map. Enrichment Map organizes gene-sets in a network and it enables the user to quickly identify the major enriched functional themes. Input: gene list from genomics experiment (statistically analyzed). Output: enriched pathways visually displayed.
Related publications: Gene-set enrichment analysis (GSEA) Enrichment Map
Example of pathway and network analysis:
- A typical example (see figure below the text) comes from gene expression data comparing treated samples versus non-treated samples. The first step is to identify differential gene expression using statistics: genes are ranked using t-test t values with up-regulated genes at the top of the list and down-regulated genes at the bottom.
- Next, GSEA is run to find out if gene-sets contain mostly up or down-regulated genes. [Gene-sets are a group of genes that have been annotated to have a similar biological function or belong to the same biological pathway e.g. mitosis and are collected from multiple databases].
- Then, Enrichment map helps visualize all the gene-sets that are significantly enriched in the treated (red circles) or in the non-treated samples (blue circles). [Each gene-set is represented by a circle, also known as a node]. If gene-sets have similar annotations, they cluster together on the map [e.g. all gene-sets related to chromosome condensation and replication fork cluster together] which ease interpretation of the map. In this example, many gene-sets related to mitosis and DNA replication/damage, or involved in the replication fork complex, are enriched in the treated samples (red nodes, genes in these gene-sets are mostly up-regulated). Gene-sets involved in ossification/bone morphogenesis are enriched in the non-treated samples (blue nodes).
- As a result, the analysis output summarizes all of the known biological function/pathways that are changing in a particular experiment and more detailed analyses can be performed as a next step to validate or to generate new hypotheses.
Predict the function of an unknown gene GeneMANIA finds other genes that are related to a set of input genes, using a very large set of functional association data. Input: a gene or set of genes. Output: connections between input genes and suggestions for additional related genes.
Related publications: GeneMANIA
We are interested in discussing custom analysis - it is how we learn what you need.
What can you expect from the service:
- We run pathway and network analysis for you and help interpret the data.
- We can help you at different stages:
- at the experimental design stage
- during the analysis: we offer training in data analysis and exploration
- after an initial analysis is complete and any validation experiments have been performed, we can book a follow-up meeting to see if you need additional analyses or to help plan subsequent genomics experiments.
Your data should have been already statistically analyzed
If you need support for your statistical analyses, please contact Shaheena Bashir (Ph.D. in Statistics) at sbashir@uhnres.utoronto.ca.
Located at MaRS TMDT 15th floor, Shaheena Bashir offers free consultation for statistical analyses for Cancer Stem Cell program (https://sites.google.com/site/biostatisticscancerstemcell/). Your data will be analyzed and output in the correct format for subsequent pathway and network analyses. You are encouraged to contact Shaheena as soon as you plan your experiment: genomics technologies can be very sensitive to noise and a well designed experiment is very important for best results. Statistical consultation at the design stage is crucial for improved data quality and results.
How to use the service
If you are a member of OICR Cancer Stem Cell program, you may use the service if
- You are planning to generate 'omics' (e.g. gene expression) data
- You have a large gene list derived from a large-scale omics project that is ready to be analyzed
- You require training in pathway and network analysis
Please schedule an appointment with us:Consulting meeting If you are planning a genomics experiment and you need some advice concerning the experiment design. Typical time: 30-60 minutes
Analysis planning meeting If you have data ready to analyze and they have been already statistically analyzed. Typical time: 60 minutes
Training session If you want to do your own pathway and network analyses, we can explain how software tools and methods work, such as GSEA, Enrichment Map and GeneMANIA. Typical time: Regular training schedule is currently being planned. Individual or group sessions can be arranged.
How to book an appointment
Normal in person meetings are on Tuesdays at TMDT 8th floor. Let us know if this doesn't work for you. Check our meeting calendar to see available times (30 min to 60 minutes meeting)
Send an e-mail to veronique.voisin@gmail.com with your preferred meeting time and the purpose of the meeting and wait for e-mail confirmation.
- For first-time meetings, please send a brief description of your project or a paper that best describes your work prior to the meeting.
If you booked an initial meeting, please read our standard operating procedure to know what to expect
If you must cancel a meeting, please give 24 hours notice to veronique.voisin@gmail.com.
Examples of pathway maps included as figures in published papers
- Metabolic adaptation to chronic inhibition of mitochondrial protein synthesis in acutemyeloid leukemia cells. Jhas B, Sriskanthadevan S, Skrtic M, Sukhai MA, Voisin V, Jitkova Y, Gronda M, Hurren R, Laister RC, Bader GD, Minden MD, Schimmer AD.PLoS One. 2013;8(3):e58367. Epub 2013 Mar 8.
- Attenuation of miR-126 activity expands HSC in vivo without exhaustion. Lechman ER, Gentner B, van Galen P, Giustacchini A, Saini M, Boccalatte FE, Hiramatsu H, Restuccia U, Bachi A, Voisin V, Bader GD, Dick JE, Naldini L.Cell Stem Cell. 2012 Dec 7;11(6):799-811.
- A comparative transcriptomic analysis reveals conserved features of stem cell pluripotency in planarians and mammals.Labbé RM, Irimia M, Currie KW, Lin A, Zhu SJ, Brown DD, Ross EJ, Voisin V, Bader GD, Blencowe BJ, Pearson BJ. Stem Cells. 2012 Aug;30(8):1734-45.
- Seventeen-gene signature from enriched Her2/Neu mammary tumor-initiating cells predicts clinical outcome for human HER2+:ERα- breast cancer. Liu JC, Voisin V, Bader GD, Deng T, Pusztai L, Symmans WF, Esteva FJ, Egan SE, Zacksenhaus E. Proc Natl Acad Sci U S A. 2012 Apr 10;109(15):5832-7. Epub 2012 Mar 28.