I have a problem with cufflinks, all the transcripts which I assemble always consist of just one exon in the resulting GTF file!
I started with fasta files, aligned them with BLAT. Converted the output to bed12. Converted the bed12 to bam with bamToBed of samtools, and sorted.
Then I used cufflinks and get a GTF file. In that GTF file, the assembled transcripts look good, but each transcript is just one exon long: there is no intron-exon structure, altough it *is* still in the bed12 file, and there are no alternative splicing pathways generated.
I am a beginner with cufflinks. Any help appreciated. Thanks.
I started with fasta files, aligned them with BLAT. Converted the output to bed12. Converted the bed12 to bam with bamToBed of samtools, and sorted.
Then I used cufflinks and get a GTF file. In that GTF file, the assembled transcripts look good, but each transcript is just one exon long: there is no intron-exon structure, altough it *is* still in the bed12 file, and there are no alternative splicing pathways generated.
I am a beginner with cufflinks. Any help appreciated. Thanks.
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