Hi, I'm new in the NGS technology. I have a problem with Bowtie paired end loading data. A few weeks ago I use galaxy to generating data from my Illumina Fastq: I convert format to fastqsanger using the convert format tab on ''edit attributes''. Now it's impossible! I convert format with fastq groomer but, when I try to starting alignment with bowtie for Illumina, I choose paired end but the software don't show me the possibility to load two fastqsanger files. I don't understand why, cause I did it some a few weeks ago...
I try to start with only one (forward file or reverse) and obviously in the bam files I see nothing. I hope to have explained my problem in a good manner (I'm not a bioinformaticist).
Thanks