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tophat -r 20 hg18_c read1.gff read2.gff
Is there any way to convert gff to fastQ format?
and How could I use -G option to read gff files in tophat?
Thanx
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Error: file SL001_R00089_RHE011final_unique.gff does not appear to be a valid FASTA or FASTQ file
Is there any way to convert gff to fastQ format?
and How could I use -G option to read gff files in tophat?
Thanx -
No, that would be meaningless. GFF files are for features on a sequence (typically a chromosome or a contig), while FASTQ for sequences with base qualities (typically single reads).Originally posted by repinementer View Post -
yes
yes sorry my bad.Comment
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