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Methylation analysis request for help

Dear All Biostars, I desperately need your help! I am really new in Methylation in rare diseases subject and have no idea how to start the analysis. I want to recreate results by working on the GEO89353 data. There are raw data available, and matrix. I want to avoid the normalization procedure and so on. I want to use R example by creating a plot with methylation fraction (Beta value) and genomic location. I even don't how to calculate the Beta value or where should I find it. I am very sorry for being so dumb but I am really new in this subject, before I was working with NGS. I want to recreate results like in the paper with GEO89353. They used lima and metyAnalysis packages. I see lima is more to normalized data and so on.

I would be very very glad if someone could guide me step by step what should I do and how to analyse :(

Thank you in advance. Dorota

r

You've asked too many questions, and the situation summarizes to "do my job for me". You need to figure out what you want to do, and it will become a series of small steps, some of which you can solve and others you can ask more pointed questions. How to make a picture, or how to perform a calculation, are two separate questions. "What are the steps involved here" is not the sort of question a web forum can handle. Find a textbook or read some journal articles very carefully, the supplemental methods section of a good paper will tell you the steps they performed in order.

Thank you, will return with more detailed questions.

Thank you Karl:) You are a good men:)

Dear Karl, I was reading carefully publication you proposed to read and also again, paper my Boss wants me to do the analysis. I have question. I want to plot the graph where y will be the Methylation beta value, x genomic locations. I have beta values for one porband, father and one more and of course the controls of MXQ gene. The paper of Barbosa et al, provided at GEO: matrix file, SOFT file and Raw files. What I understand I have to use the matrix? What I mean I have a problem with understanding the x on the plot (genomic location). I know on which location of the gene they used, and I have such information but have no idea where to find the exact location to create the plot like they did. I have only the range of the genomic location.

Here is the link to the publication :enter link description here I want to recreate the Figure 1A.

I am very sorry I am still asking but I really don't know where to find the answer. ps. If you can and would like to help me here is email dorotabuczek81@gmail.com

1 answer

Linked thread and answer: A: Normalization of the Illumina HumanMethylation450 BeadChip data, platform GPL135

Kevin

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