Open sparthib opened 4 months ago
Hi Sowmya,
The first two warnings are more informational, than detrimental to your analysis. The first can occur when there are reads to scaffolds in the fasta file, that have no annotations in the gtf file, for example on accessory chromosomes, which is quite common. The second is a consequence of some aligners which can align part of a read near the end of scaffolds, but the entire read extends beyond those boundaries. I have observed this myself in my own data and we havn't come up with a clean solution, which is why we only report how many reads we remove from the analysis, so users can know how much of their data is impacted.
The third warning however is critical. By default bambu expects spliced reads, and in most use-cases they should be present in the data. The most typical cause for a lack of spliced reads is either the user mapped the reads to the transcriptome (which doesn't seem to be the case in this instance), or they ran an aligner such as minimap2 without setting the splice aware parameter.
Let me know how you aligned your data, or if you don't expect spliced reads (prokaryote sample, targeted amplification sequencing etc), and we can go from there.
Kind Regards, Andre Sim
Hi Andre,
Thank you for your quick and detailed response. I believe this is because I ran minimap2 without setting the splice aware parameter. Will update this thread after rerunning alignment.
Thanks! Sowmya
Hello, I have a bam file where my reads are aligned to the
GENCODE GRCh38.p14.genome.fa file
. The corresponding gtf file isgencode.v44.chr_patch_hapl_scaff.annotation.gtf
I tried running BAMBU in discovery only mode
I reloaded the output rcFile as
In my resulting se file, I see these 3 warnings in the metadata:
Also, for each transcript in my
bambuAnnotations
object, I see the following message as well.505 sequences from an unspecified genome; no seqlengths
I seem to be using matching reference genome fastas and gtfs. Any pointers as to what could be wrong would be appreciated.
Thanks,
Sowmya