NUStatBioinfo / DegNorm

Normalizing RNA degradation in RNA-seq data
https://nustatbioinfo.github.io/DegNorm/
3 stars 1 forks source link

some help running degNorm #48

Closed dllahr closed 1 year ago

dllahr commented 1 year ago

Hi

First, thank you for providing the degNorm tool (and writing the paper describing it) - it seems like a great resource - very much appreciated.

I'm writing to ask for some help / guidance in running the tool (details of setup / command below.). I'd like to get a sense of if I'm heading in the right direction or not, a rough sense of the compute required to run, any guidance would be very helpful and much appreciated:

Here's the command I used to run:

nohup degnorm --bam-files $(cat input_bam.grp ) --bai-files $(cat input_bai.grp ) \
-g gencode.v27.primary_assembly.annotation.gtf \
-p 8 -o output &> degnorm.log &

I'm using an AWS EC2 instance t3a.2xlarge (8 CPUs, 32 G RAM) running AWS linux (CentOS variant). Installation of degnorm was normal, tests passed.

Any ideas / suggestions would be much appreciated - thank you in advance, Dave

ffineis commented 1 year ago

Hi Dave,

Apologies that the program has been slow on your 9 samples. The python CLI tool is memory inefficient, and does not make proper use of multiprocessing during the NMF routine, leading to long processing times. I am no longer actively maintaining this repo and highly recommend that you switch to using the more optimized R library.

I will leave an archive notice on the python package's README file this week with plans to archive in March 2023.

Thanks, Frank

dllahr commented 1 year ago

Thank you for the response - much appreciated. I'll try that out.