Hi
I am new to bioinformatics and have never worked with 454 PE sequences before. I have 454 PE reads in fasta file format. The sequencing was done on the Roche 454 Titanium platform.
My understanding is that 454 results are stored in .sff files, from which sequence and quality data must be extracted.
Is it safe to assume, then, that if I have fasta files the forward and reverse ends have been separated already? I only have one file, not two.
Is it possible for the ends to still be joined in the fasta file? If so, how can I tell if the PE sequences have been separated already?
Can anyone suggest tools for doing the separation if I need to? I've found pyrocleaner and the NGS QC Toolkit, but I have no experience with either of them.
thanks!
E
I am new to bioinformatics and have never worked with 454 PE sequences before. I have 454 PE reads in fasta file format. The sequencing was done on the Roche 454 Titanium platform.
My understanding is that 454 results are stored in .sff files, from which sequence and quality data must be extracted.
Is it safe to assume, then, that if I have fasta files the forward and reverse ends have been separated already? I only have one file, not two.
Is it possible for the ends to still be joined in the fasta file? If so, how can I tell if the PE sequences have been separated already?
Can anyone suggest tools for doing the separation if I need to? I've found pyrocleaner and the NGS QC Toolkit, but I have no experience with either of them.
thanks!
E
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