Hi,
I'm trying to perform RNA sequencing differential expression analysis on the GEOdataset GSE111320 in the R program. https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE111320
Does anyone know how I might create one count file when the dataset has 40 xls.gz files?
Thank you
2 answers
I would say it's impossible given that the files attached to the experiments do not include counts by genes and instead are some sort of fusion annotation.
EDIT: So the solution is to download their raw FASTQ and do the rna-seq analysis manually
I do not know what these files contain. Anyway, use https://maayanlab.cloud/biojupies/analyze/search?q=gse111320&organism=all&sortby=new&min_samples=6&max_samples=500
BioJupies provides raw counts and metadata. Click through the early analysis and in the end you get a section to download the raw counts. Use that, won't get easier than that. BioJupies is great for that as it contains thousands of preprocessed datasets for a quick analysis. You can still download fastq from GEO later and process as you like if the data turn out to be useful for your question.
Log in to answer this question.