Hi Prasad, Thanks for the reply On a second look, the mirbase sequences are in fasta format while Bowtie takes fastq reads for alignment. is there a way around this?
Please help, I am new to sequence analysis. I have been trying to create gff/gtf annotation file for mature miRNA sequences obtained from miRBase in order to analyze some sequence data. I have not seen any directions on how to achieve this. The miRNA sequences are in fasta format and I have my reference genome sequence too. Please kindly guide me. Thank you
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I got that resolved, Prasad But I got the sam file of the alignment. When I tried to run the perl script to convert the sam file to gff i got a fatal error "Unable to open input file <filename.sam>".
My command perl scampi_sam_to_gffv1.pl -i inputfile.sam -o outputfile.gff
Is the sam file not in current directory? Have you tried ./inputfile.sam to make the location more explicit?
Yes it is in the current directory. i also had to specify the path explicitly when i got the error, still got the error.
Can you post a few lines of your sam file?
head inputfile.sam
Sure. Here is the output
@HD VN:1.0 SO:unsorted
@SQ SN:Chromosome01 LN:34959721
@SQ SN:Chromosome02 LN:32431396
@SQ SN:Chromosome03 LN:29412403
@SQ SN:Chromosome04 LN:28749345
@SQ SN:Chromosome05 LN:28438989
@SQ SN:Chromosome06 LN:27939960
@SQ SN:Chromosome07 LN:27069033
@SQ SN:Chromosome08 LN:34011518
@SQ SN:Chromosome09 LN:29417918
That looks like a proper sam file (assuming you see alignments further down in the file, correct?).
yes it is
This is more of the file
cel-lin-4-3p 4 * 0 0 * * 0 0 ACACCTGGGCTCTCCGGGTACC IIIIIIIIIIIIIIIIIIIIII XM:i:0
cel-lin-4-5p 4 * 0 0 * * 0 0 TCCCTGAGACCTCAAGTGTGA IIIIIIIIIIIIIIIIIIIII XM:i:0
cel-miR-1-5p 4 * 0 0 * * 0 0 CATACTTCCTTACATGCCCATA IIIIIIIIIIIIIIIIIIIIII XM:i:0
cel-let-7-5p 4 * 0 0 * * 0 0 TGAGGTAGTAGGTTGTATAGTT IIIIIIIIIIIIIIIIIIIIII XM:i:0
cel-let-7-3p 4 * 0 0 * * 0 0 CTATGCAATTTTCTACCTTACC IIIIIIIIIIIIIIIIIIIIII XM:i:0
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Thank you Prasad. I will try the SAM2GFF out and revert