I have a question to the de novo assembly using cufflinks: is there a threshold to join two non-overlapping reads?
As you can see from the attached figure, the top track is for alignment (BAM file from Tophat for non-strand-specific RNAseq), and the lower track is assembly from cufflinks. I run this simply as
cufflinks input.bam
It's for sure that overlapped reads are joined together into one isoform (or transfrag). What's strange for me is, why some separated reads (with gap between) are also joined, but some are not. As you can see, there are 4 gaps in the top track, where the first and last gap are not joined, while the 2nd and 3rd ones are joined. I guess it's because of the smaller gap distance in 2nd and 3rd gap, but I cannot find such 'gap threshold' in the cufflinks options.
I also tried the command with options:
cufflinks --min-intron-length 100
and
cufflinks -F 0.0 --trim-3-dropoff-frac 0 --trim-3-avgcov-thresh 0 --min-frags-per-transfrag 1 --min-intron-length 100
both don't change the result.
I appreciated if any could explain this to me. Thanks a lot.
As you can see from the attached figure, the top track is for alignment (BAM file from Tophat for non-strand-specific RNAseq), and the lower track is assembly from cufflinks. I run this simply as
cufflinks input.bam
It's for sure that overlapped reads are joined together into one isoform (or transfrag). What's strange for me is, why some separated reads (with gap between) are also joined, but some are not. As you can see, there are 4 gaps in the top track, where the first and last gap are not joined, while the 2nd and 3rd ones are joined. I guess it's because of the smaller gap distance in 2nd and 3rd gap, but I cannot find such 'gap threshold' in the cufflinks options.
I also tried the command with options:
cufflinks --min-intron-length 100
and
cufflinks -F 0.0 --trim-3-dropoff-frac 0 --trim-3-avgcov-thresh 0 --min-frags-per-transfrag 1 --min-intron-length 100
both don't change the result.
I appreciated if any could explain this to me. Thanks a lot.
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