Closed BGI2016 closed 3 days ago
Hi @ibn-salem @priesgo @ozlemmuslu @martinloewer @mostafiz2010
I have also met this problem with paried rna-seq fastq.gz files of 29 samples(2 ~3G 29samples). Within them 24/29 succeed in the output but the remaining 5 samples were stuck in the soapfuse prediction step (4 samples, succeed in upstream prediction steps) or in the fetchdata step ( 1 sample, succeed in upstream steps). I have to ended related slurm jobs while running for 7 days. Could you help me with this problem?
Really glad to get your replies. If you want more detailed information please just contact me. Thank you so much!
Best regards, Tesson
@Tesson98 @priesgo I also encounter the same problem. When I use Docker to run EasyFuse, I always report an error in the fetchdata.py step.
I also encounter extremely long run times, and then soapfuse will die randomly....
The runtime should be improved in the latest EasyFuse versions. If not please open a new issue. Thanks.
Hello @ibn-salem @priesgo @ozlemmuslu @martinloewer @mostafiz2010 My data is 260 million distinct sequencing reads(2×150 nt).When I predicted GFs with the Easyfuse 1.3.6 from my data, the software ran for eight days. why run time is so long?Hope to get your reply.
Kind Regards, Lily