Hello all. I am trying to map some fasta files I generated from a TE.bed file. But I get the segmentation fault:11 error. some suggest its a memory problem and for that reason I tried to avoid outputting unaligned reads but it didnt help either. below is my command.
bowtie genome.index -f TE.fasta --un unal.fa --al al.fa -S out.sam
I would appreciate your suggestions please. Thanks
did you use the precompiled binary? In case you did there might be incompatibilities which lead to the segmentation fault. Potentially you missed something in the stacktrace pointing to some lower level dependency? In this case, give it a try and compile from source.
Is there a reason for choosing bowtie over bowtie2?
The fasta was generated as follows, bedtobam then bedtools getfasta to make fasta from bam. I dont understand what you mean by precompilled binary and compile from source. Also, I chose bowtie instead of bowtie2 because Im trying to map si and piRNA overlaps with a python script.