Movatterモバイル変換

Thanks for all the inputs.

Since you have publications associated with this data (based on your last thread and a question before that) don't try to do this analysis …

Thank you so much, you were really helpful!Do you think it is possible to do some kind of analysis to evaluate positive selection or mainl…

I doubt your RNA quality is the issue. It's not likely that poor quality would cause reads to align to the wrong gene. Its far more likely …

The RIN values for these samples ranged around 6.0-7.0, which I think would suggest RNA degradation. From what I am aware of, I don't think…

You can do a de novo assembly and then scaffold the contigs using a reference by RagTag (https://github.com/malonge/RagTag). However, I per…

The difference between (A or T) and (G or C) may reflect the GC composition of the genome. Thus, it is not indicative of some sequencing pr…

What do you mean by "non-raw" data? You're correct in that grabbing arbitrary values on different scales and trying to mash them together i…

None of the tags you used are relevant to the question you asked - they broadly describe the entire field of bioinformatics. I've fixed it …

Hi @slzr_In short, no. What I mean is, it’s generally not recommended to use Mutect2 calls directly for classical population genetics ana…

Please note also that there are also forums that directly relate to CPTAC (only), which may be more appropriate depending on the nature of …

Try ggnewscale package, add new_scale_color() between the plots. Something like this should work ggplot() + geom_line(data = gr…

You are trying to colour the same gene names with two different codes. Either make two subplots for the groups or change the shape of dots …

Considering your suggestion, I'd like to elaborate what I wish to find. I started with proteomics analysis form TCGA data obtaining the pro…

Thank you @LChart, wow that sounds like a very elegant solution! I've got the seurat currently in R. I'll export to python and give it a ba…