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Hi, thanks for reaching out. I'm sorry that we don't have a function for reseeding a circular sequence currently, which may involve accurate annotation. |
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Hello,
I don't know what you mean by reseeding? I am using a complete mtDNA
genome with an annotation as a seed but the seed starts at different gene
than my assembled mtDNA from getorganelle. Is there a way to get my new
assembly to start at the same gene? This is the command I'm using
get_organelle_from_reads.py -1 DS18041_R1.fastq.gz -2 DS18041_R2.fastq.gz
-k 21,45,65,85 -s Hassanin_2012_JN632670.fasta --genes gene.fasta -F
animal_mt -t 32 -o odocoileous_mitogenomes_4
…On Wed, Jan 18, 2023 at 9:12 AM JianjunJin ***@***.***> wrote:
Hi, thanks for reaching out. I'm sorry that we don't have a function for
reseeding a circular sequence currently, which may involve accurate
annotation.
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Thank you for clarifying. It would be a nice feature. I was hoping I just
might have missed something in the getorganelle manual.
Thanks again.
…On Wed, Jan 18, 2023 at 1:59 PM JianjunJin ***@***.***> wrote:
Sorry about the unclear of what I meant by using an improper word reseed -
I meant to restart a circular sequence.
I totally got your point. The clear answer should be there is currently no
way of doing that automatically through GetOrganelle.
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I have been thinking about that because there are many demands, including
getting a new start for a circular genome and picking the structure looking
more like the reference when there are multiple structures. But I can only
work on that after pushing on other issues. It is more like a downstream
treatment but will be useful. I can keep you posted if it is available, but
it will be a while.
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Hi,
I was wondering if there is a way to choose a specific gene to start the completed mtDNA genome from? For example, start the scaffold at tRNA-Phe. In the scaffold getorganelle assembled for me tRNA-Phe is at position 11,175, and I would like it to be at position 1.
Thank you for your time and suggestions.
-Josh Hallas
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