How to merging multiple GSEs with different GPLs?
I want to merging multiple GSEs with different GPLs(with R) ,but I don't know which package is suitable for merging, for this purpose, VirtualArray and InSilicoMerging packages do not efficient.
r
• 1,475 views
•
link
written
by
maryam.sabet •
0 answers
No answers yet.
Log in to answer this question.
More posts like this
-
Can I use method 'GSVA/ssGSEA' in different GSE/RNASeq data with different PlatForm?
written by daillythings_zhou •I want to do some meta analysis using GEO datasets, it contain different PlatForms microarray data and RNASeq data.(different PlatForms, contain different probes,) I have …
-
There is a convenient way to use not up-to-date packages in R?
written by yussab •Hi everybody, I'm trying to replicate an article from 2018, in which they used these two packages: InSilicoDb: https://www.bioconductor.org/packages//2.13/bioc/html/inSilicoDb.html InSilicoMerging : https://www.bioconductor.org/packages//2.13/bioc/html/inSilicoDb.html I'm not able …
-
Plot selection suggestion
written by K.Gee •Hello. I have 10 sets of core genes (homologous core genes families families from 4 different genomes), and I want to make a plot like …
-
Genotype analyzing of infinium illumina bead array
written by hasani.iut6Hi. I am interested to analysis genotype array of Illumina: Infinium. I search a lot for different package and software that are good for my …
-
Problem with working with "methAnalysis" package in R
written by nazaninhoseinkhanDear all, I want to analyze microarray methylation data to find differentially methylated regions. First I tried to work with Galaxy, but I did not …
-
Contig length distribution plotting with R
written by seta<p>Hi all,</p> <p>I would like to plot the contig length distribution of my assembly using R software. I tried the ggplot2 package, but sounds that …
-
Adding a variable as a varlabel to my dataset
written by Shamim SarhadiI have 2 gene expression and after merging them with insilicomerging package I want to drow a MDSplot but it needs that my dataset has …
-
How to analyse normalized read count?
written by pbioI have read counts for two samples coming from different data center, which are normalized using house keeping genes and got the relative expression for …
-
INSILICOMERGING: Error in (function (classes, fdef, mtable)
written by ira_grich •Hi , I am using Bioconductor/R and `inSilicoMerging` package. I got an error message: INSILICOMERGING: Run with no additional merging technique... **Error in (function (classes, …
-
Finding Differentially Expressed Genes Across Multiple Cell Types In A Datset
written by Bioinfo_2006<p>I have a transcriptome dataset from affymetrix microarray and has multiple cell types which were probed. I would like to obtain the differentially expressed genes …
Could you explain what are you trying to do? GPLs describe different GEO platform (Sequencing, array or even RT-PCR) and unless they are measuring similar things, you can not merge them. On the top of that, you need to care about different normalization and overall normalization of merged samples.
I want to find similar genes between different GPL then compare expression level of these genes to find out which have significant difference.