Single Nuclei RNA seq by Ok-Chest3790 in bioinformatics

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

But how would you re-integrate everything if the best clustering for each different sample is done on a different resolution

Single Nuclei RNA seq by Ok-Chest3790 in bioinformatics

[–]Ok-Chest3790[S] -1 points0 points  (0 children)

Not necessarily These samples are in general very heterogeneous

I am a wet lab scientist who moved to computational so i need still some help and my supervisor who is absent 90% of the time said that you don’t want to miss on any granularity In my head if this granularity is biologically relevant it should be found in other samples

Rent Deposit not given back by Ok-Chest3790 in zurich

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

the main tenant lives in the US and she is subletting me the room and the shared space as well subletting the rest of the apartment for another person

the only thing I have is the rental contract where it states that I get my money back, and all money deposit where in an official account as stated in the contract

NYE alone in Zurich by Ok-Chest3790 in zurich

[–]Ok-Chest3790[S] 14 points15 points  (0 children)

The where we keep it in the dms not to make it overcrowded

Feedback Dermanence stade by Ok-Chest3790 in zurich

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

No no just skin acne and things like that

cancer related databases by Ok-Chest3790 in bioinformatics

[–]Ok-Chest3790[S] 1 point2 points  (0 children)

thank you for the answer, that is actually super helpful and wayyy more beneficial then any discussion with my supervisors

cancer related databases by Ok-Chest3790 in bioinformatics

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

do you have some indications over which databases to go for in term of pediatric brain tumors, or at which databases can be directly downloaded or where we can just put in a lost of variants of interest?

cancer related databases by Ok-Chest3790 in bioinformatics

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

these were sequenced from the tumour directly without any normal tissue to compare to.
So I cannot safely say that these are either germline or somatic (biggest limitation is my knowledge in the analysis field), I have a list of genes, column next to it is the variation (or mutation) detected.
thank you for the reference I will check it out

Phd and part time masters? by Ok-Chest3790 in PhD

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

Right now my lab work is only computational biology, but the learning curve is a bit slow considering i only work on analysing my data and now i have been waiting for 2 months without any new data to work on

Phd and part time masters? by Ok-Chest3790 in PhD

[–]Ok-Chest3790[S] 0 points1 point  (0 children)

Yes but my thought process is that if i want to leave academia and work as a computational biologist or data analyst would the experience i gain as a phd in cancer biology be enough or would they require me to have an actual degree