Exact(12)
Biases in the starting positions of reads become apparent when looking at the other analyses.
As longer sequence reads become available, it will be possible to identify considerable structure flanking a given AS event.
Another advantage of storing the alignments without the underlying sequences is that it saves space, especially as reads become longer.
We expect our method to be more useful in the future as the sequence reads become longer.
Therefore, it is expected that ~6%23%3% * 0.33) of the mapped reads become unmapped without the use of a gene model.
Using NGS technologies, it is a commonly accepted observation that the longer reads become, the more prone they may be to errors [ 29].
Similar(48)
Without a gene model, 3%to9%9% of non-junctions reads became multiple mapped reads.
When the reads became available, the transcripts were corrected on the basis of the reads.
Additionally, the estimation of genomic signatures in sequencing reads becomes increasingly difficult for decreasing read lengths.
When the RNAseq reads became available, if possible, the putative transcripts were corrected on the basis of the reads.
Therefore, the question of whether one can accurately predict full-length transcripts from these reads becomes important.
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