Hello, I tried to aligned paired end reads with BWA (Map with BWA (version 0.2.3)) on my own Galaxy server. However, I am not able to select any FASTQ files from the history, because I got this error `Select first set of reads: History does not include a dataset of the required format / build`.
This is it the output from FASTQ:
Filename: SRR512904_1.fastq
File type:Conventional base calls
Encoding: Sanger / Illumina 1.9
Total Sequgences: 23282596
Sequences flagged as poor quality: 0
Sequence length: 76
%GC: 53
Filename: SRR402883_2.fastq
File type: Conventional base calls
Encoding: Sanger / Illumina 1.9
Total Sequences:143366953
Sequences flagged as poor quality: 0
Sequence length: 76
%GC: 53
How is is possible to make the reads visible in BWA?
Thank you in advance.
