Question: Analysis Of Putative Causitive Mutations
gravatar for Kamila001
8.0 years ago by
Kamila001120 wrote:

I have set of predicted causitive missense mutations by using Insilico tools like SIFT, SNAP, SNPEffect, Polyphen etc.. The question is What would be the best way to further analyze them (bioinformatics tools or statistical methods or grafically)? e.g. could do the gene ontology analysis to see their biological role.

Any suggestions about softwares and literature would be useful.

Thanks in advance.

function statistics • 2.0k views
ADD COMMENTlink modified 8.0 years ago by Khader Shameer18k • written 8.0 years ago by Kamila001120
gravatar for Pauline Ng
8.0 years ago by
Pauline Ng110
Pauline Ng110 wrote:

Hi Kamila,

This is Pauline Ng, creator of SIFT (please note new website located at: The answer would depend on what type of analysis you are doing.

Genome-wide: If you are doing a genome-wide analysis, for seeing what genes in a Drosophila species are affected and have evolved differently, then use GO ontology like GOrilla to find any patterns. Also, if it's a genome paper, use Ka/Ks to see if the genes which contain these predicted-deleterious predictions are under relaxed selection, or the gene family size to see if the substitutions occur in large gene families. Ka/Ks and gene family size can be obtained from Ensembl Biomart. I like scanning the list of genes manually, see if any patterns strike out at me, and then code it up accordingly.

Finding a specific gene: If you are looking for a specific gene (for example, looking for a disease gene, and you know the disease), then you would list the gene descriptions, and whether any are in OMIM (just use the checkboxes on the website), and then look through them manually to see if any are interested hits. This may or may not get what you want, if you know the disease name, then use tools like Endeavour where you can enter the disease, or genes involved in the disease, and then all your genes that were predicted to affect protein function, for prioritization of candidate disease genes. There are a class of tools out there that do this (Endeavour, G2D, etc.)

Hope this helps. Again, please check out our new website at where I am adding the latest updates.

Best, Pauline Ng

ADD COMMENTlink written 8.0 years ago by Pauline Ng110

Thank you very much Pauline for such a detailed answer. I am working on the Genome wide analysis and will surely look at the Ka/Ks and gene family using Biomart. If I am not wrong this means may be by using Ka/ks we are also trying to figure if any candidate gene is psuedogene or not? or this will tell simply the selection pressure?

ADD REPLYlink written 8.0 years ago by Kamila001120

Hi Kamila,

In the strict sense, evolutionary biologists typically consider Ka/Ks ~ 1 as under neutral selection, and hence pseudogenes. Enough evolutionary time has to pass in order to get Ka/Ks ~1 -- if you compare your species to another species that's too closely related, there may not be enough genome changes to accurately measure Ka/Ks. Another way to tell pseudogenes is if there are frameshifting indels or stops compared to a functional gene.

Best, Pauline

ADD REPLYlink written 8.0 years ago by Pauline Ng40
gravatar for Khader Shameer
8.0 years ago by
Manhattan, NY
Khader Shameer18k wrote:

Short answer: you can perform impact of mutation in transcriptome, epistasis analysis, pathway analysis, protein-protein interaction analysis, TF analysis, eQTL analysis, phenotype analysis are some potential ideas that you could explore.

Long answer: I would point you to three recent review articles and one community articles that discuss various potential ideas on post-gwas bioinformatics and statistical strategies. Most of the ideas are discussed with atleast one example, so you can definitely get a clear idea by reading the key-papers discussed in the review articles.

Review 1: Prioritizing GWAS Results: A Review of Statistical Methods and Recommendations for Their Application

Review 2: Bioinformatics challenges for genome-wide association studies

Review 3: Using biological knowledge to uncover the mystery in the search for epistasis in genome-wide association studies.

Post-gwas article : Principles for the post-GWAS functional characterisation of risk loci

ADD COMMENTlink written 8.0 years ago by Khader Shameer18k
Please log in to add an answer.


Use of this site constitutes acceptance of our User Agreement and Privacy Policy.
Powered by Biostar version 2.3.0
Traffic: 888 users visited in the last hour