Open changchuanjun opened 3 months ago
If you deal with huge amounts of RNA-Seq, you can align, convert, merge, and sort before providing the merged BAM file to BRAKER. That's how I usually do it.
Note that adding more and more RNA-Seq does not necessarily improve results. I sometimes alternatively skip technical and biological replicates...
@KatharinaHoff , Thank you for your response. When aligning my RNA-seq data to the corresponding soft-masked genome, I noticed only a slight difference compared to the hard-masked genome. Is it correct?
Yes the results will differ. They may even differ drastically. The aligners usually ignore softmasking, it's like unmasked.
On Thu, Mar 14, 2024 at 2:15 PM Changchuanjun @.***> wrote:
@KatharinaHoff https://github.com/KatharinaHoff , Thank you for your response. When aligning my RNA-seq data to the corresponding soft-masked genome, I noticed only a slight difference compared to the hard-masked genome. Is it correct?
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In my result, the predict result (the number of gene) of BRAKER3 is slightly different between hard masked genome and soft masked genome. Is it correct?
It depends on the genome. Differences can be small or huge
Changchuanjun @.***> schrieb am Do. 14. März 2024 um 14:37:
In my result, the predict result (the number of gene) of BRAKER3 is slightly different between hard masked genome and soft masked genome. Is it correct?
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Hello, thanks your team for developing BRAKER pipeline accessions which promote community to finish gene structure annotation. When I ran BRAKER3(v) pipeline to annotate my genome,I found this programme could not delete .sam file when complete samtools sort step which can convert sam file to bam file. sam file is too large and occupies too much space(dozens of Gb).