Open adiv5 opened 1 year ago
Hi @adiv5
I'm not entirely sure I understand your question. You can use the st_pipeline
to process the raw data (FASTQ) to obtain a matrix of counts (spots by genes). This matrix can be used, together with the HE image, for downstream analyses such as the one you mention but the st_pipeline will not do that for you.
Best, Jose
Hi, I am trying this out on the example visium10x dataset for prostate cancer (https://www.10xgenomics.com/resources/datasets/human-prostate-cancer-adenocarcinoma-with-invasive-carcinoma-ffpe-1-standard-1-3-0)
My end usecase is to have a basic Image Model that could predict gene expression for a given gene on the entire tissue on cell level
in this data, in the input files section, we have Fastq files and a probeset file thats it. For the other output files im not sure if those could be used / need to be used in here.
If you could help with some concrete steps to use this , it would really help a lot.
Thank you in advance.