I have uploaded some of ChIP-seq compressed as gz to Galaxy. After uploading, those gz file become as fastq format automatically. I don't have any idea why Galaxy couldn't run those fastq files on embedded tools like BWA except for FastQC.
Did I miss some things? Could anyone know how to do?
Here is some reads in Fastq of my chip-seq:
@HISEQ:163:HBBYRADXX:2:1101:1396:2085 2:N:0:ACACGA
ACAATGCCGACTGTTCAGCCATGGATAGTCCTTTGCTTTATCTGCTTCTA
+
BBBFFFFFFFFFFFIIIIIIIIIIIIIIIIIIIIIIIIIIIIIFFFIIII
@HISEQ:163:HBBYRADXX:2:1101:1404:2105 2:N:0:ACACGA
ACAGGCACCTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTAGAGAT
+
BBBFFFFFFFFFFIIIIIFIIIIIIIFIFIIIIIIFFFIBIIFBFIFFII
@HISEQ:163:HBBYRADXX:2:1101:1495:2196 2:N:0:ACACGA
AATCTCGAACCCAGGAGGTGGAGGATGCAGTGAGCCAAGATCGCACAACT
+
BBBFFFFFFFFFFIIIFFFFFIIIIIIIIIFIIIIIIIIIIIIIFIIIIF
@HISEQ:163:HBBYRADXX:2:1101:1522:2023 2:N:0:ACACGA
GCAAAGTATAAAAGAAGAAGAAGGAGTGGGAAGAGCGCTGTAGGAAGATT
+
0<0000000<00<B000000<<0<0B0<B#####################
@HISEQ:163:HBBYRADXX:2:1101:1546:2036 2:N:0:ACACGA
CTCTTGCGCCTTCCTAGCGGCGATGTTGTCCGGGTGGTAGCGACTGCGCG
+
BBBFFFFFFFFFFIIIIIIIIIIIIBFFIBFIFI<FFBFFFFFFFFFFFB
Wei-Ming