Dear All
I am facing a problem with bowtie. I generated a library using MetaSim software for two viruses (Serotypes). I used an empirical error model, and --><-- as read pairs layout, the number of reads is 5000.
I am trying to paired-end align this data in Bowtie using the following command:
bowtie -S ebwt_file -f -1 reads_1.fasta -2 reads_2.fasta file .sam
The problem is that Bowtie is giving very poor results when the command above would executed:
# reads with at least one reported alignment: 16 (0.32%)
# reads that failed to align: 4984 (99.68%)
While i am expecting to see the opposite figure. However; both ends are aligned perfectly when i ask Bowtie to align them individually.
I need to align both ends as a pair using Bowtie, i can't work out what might be the reason behind these poor results. I tried to find out a pattern by examining the pair-algined reads ( 0.32% which is 16 reads), but i failed to find any interesting figures.
Many thanks
I am facing a problem with bowtie. I generated a library using MetaSim software for two viruses (Serotypes). I used an empirical error model, and --><-- as read pairs layout, the number of reads is 5000.
I am trying to paired-end align this data in Bowtie using the following command:
bowtie -S ebwt_file -f -1 reads_1.fasta -2 reads_2.fasta file .sam
The problem is that Bowtie is giving very poor results when the command above would executed:
# reads with at least one reported alignment: 16 (0.32%)
# reads that failed to align: 4984 (99.68%)
While i am expecting to see the opposite figure. However; both ends are aligned perfectly when i ask Bowtie to align them individually.
I need to align both ends as a pair using Bowtie, i can't work out what might be the reason behind these poor results. I tried to find out a pattern by examining the pair-algined reads ( 0.32% which is 16 reads), but i failed to find any interesting figures.
Many thanks
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