Closed jwidmann closed 8 years ago
SNAP should be able to handle any number of input reads - more likely this is a bug. I am currently working through some SNAP bugs to see if I can pin down what causes them and ask the SNAP developers to fix them.
Have you tried running the same command again? The bug may be non-deterministic, in which case it might work the second time round.
Yep, tried twice the same command, resulting in the same Error. But maybe the third time is the charm, i'll give it another try. Thanks for your fast reply :)
Ah, and please make sure to delete the output directory from the earlier runs, or give the new run a different output location.
Hmm, the next release gives the same error (but line 2283). Mapping only this specific read set works fine.
hi @jwidmann, the latest release of transrate v1.0.3 now includes the latest version of SNAP and Salmon as well as some other bug fixes. Please update and try your analysis again. Hopefully this will solve the problem - if not please re-open the issue. Many thanks for your patience :)
Hi, @blahah ,I installed the latest version of transrate v 1.0.3. But I still got the same followoing message about SNAP failed. Would you please help on it? Thanks!
[ERROR] 2017-02-23 16:07:32 : Snap failed Welcome to SNAP version 1.0dev.96.
mmap failed. MemMapDataReader: fail to map /home/jjduan/python/01highQualityData/withoutN-trimlastbase/110902_SN132_B_L002_R2_GLQ-13b.fastq at 0,1966390515 SNAP exited with exit code 1 from line 2283 of file SNAPLib/DataReader.cpp
Hi, i get the following Error when running transrate on my assembly:
Is this simply because I have too much input reads for SNAP to map, or is this something else? This is the command I used:
transrate --assembly Trinity_allTissues.fasta --left Tissue1_left.fastq,Tissue2_left.fastq,Tissue3_left.fastq,Tissue4_left.fastq,Tissue5_left.fastq --right Tissue1_right.fastq,Tissue2_right.fastq,Tissue3_right.fastq,Tissue4_right.fastq,Tissue5_right.fastq --threads 8 --output /Transrate
Any suggestions? Best wishes