Comments (2)
The ERG fusion status has been determined using gene expression; for some samples, only gene expression has been determined, while for others copy number alterations are available. We don't have full coverage over all omics.
MultiAssayExperiment does support operations that do pick samples that have information available; using some of the MAE-object functionality may prove useful: https://www.bioconductor.org/packages/devel/bioc/vignettes/MultiAssayExperiment/inst/doc/QuickStartMultiAssay.html
I'm yet to explore all of the options myself, but they seem to have covered it rather nicely. If there are some samples which should have CNA data but don't have it in the MAE-object, then those we can try fill - but it can also be that GDC (where we pull GEX and CNA data from) never processed them.
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Awesome, i'll take a closer look at the vignette. Thank you for the clarification!
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Related Issues (20)
- Splitting apart OSF portion of TCGA HOT 2
- Purity Estimates HOT 2
- Abida et al focus on polyA / TCGA focus on TPM normalized GEX (OSF) HOT 1
- Risk score benchmarking HOT 1
- Gene ID aliases alter between datasets, especially older annotation ones HOT 2
- Row names HOT 1
- Benchmarking description HOT 1
- Double-checking ranks of newly normalized data HOT 1
- Include normal samples in Taylor et al. HOT 1
- Use the generic identifiers PCA#### / PAN#### in Taylor et al. HOT 1
- Sample IDs in Clinical data - Taylor et.al. HOT 2
- Fusion status HOT 1
- Wang et al identifiers mismatch in derived variables HOT 1
- Weiner et al. & newly generated GEX for CIBERSORTx
- Cibersort results for Weiner et al. missing HOT 1
- colData does not work for MAE Barwick HOT 1
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- cBioPortal hg19 to hg38 liftOver HOT 1
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