You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
STAR 2.3.0e
Linux dna 3.2.0-41-generic #66-Ubuntu SM
THIS WORKED:
* The fasta file is a 2.8 Mbp bacteria
STAR --runMode genomeGenerate --genomeDir ref --genomeFastaFiles 6008.fna --runThreadN 32
THIS CORE DUMPED:
* Read file is FASTQ, 31bp reads, in Phred+64 format.
Core was generated by `STAR --genomeDir ref --readFilesIn 6008_mRNA.fastq
--runThreadN 32'.
Program terminated with signal 11, Segmentation fault.
#0 0x0000000000405e4b in compareSeqToGenome(char**, unsigned long long,
unsigned long long, unsigned long long, char*, PackedArray&, unsigned long
long, bool, bool&, Parameters*) ()
Original issue reported on code.google.com by [email protected] on 6 Jun 2013 at 6:07
The text was updated successfully, but these errors were encountered:
I went to the forums and dug around.
It seems to work if I add "--genomeSAindexNbases 2" to the index generation
step, as suggested by another user for small genomes.
I still consider a core dump a bug however :-)
Could you stat() the genome files to estimate the genome sizes and auto-choose
good parameters to avoid this problem?
Original issue reported on code.google.com by
[email protected]
on 6 Jun 2013 at 6:07The text was updated successfully, but these errors were encountered: