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It would be neat to be able to run isovar on many .bam samples to see how allele-specific expression changes with treatments/time. The specific use-case I have in mind is the change in expression of variant containing transcripts in a cell line with a known genotype in response to exposure to some stimulus.
At present the I'm running isovar on each sample individually, and then cobbling together a table from the results.
The text was updated successfully, but these errors were encountered:
@julia326 and I just ran into needing to pool multiple BAM files together from a single sample. What's the best interface for distinguishing between "one BAM per sample" vs. "many BAMs, single sample"?
One idea is to have --bam A.bam --bam B.bam --rna-multiple-samples vs. --bam A.bam --bam B.bam --rna-combine-alignment-files. What do you think?
Hey,
It would be neat to be able to run isovar on many .bam samples to see how allele-specific expression changes with treatments/time. The specific use-case I have in mind is the change in expression of variant containing transcripts in a cell line with a known genotype in response to exposure to some stimulus.
At present the I'm running isovar on each sample individually, and then cobbling together a table from the results.
The text was updated successfully, but these errors were encountered: