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Hi I am working on a triploid species which is highly heterozygous, see genomescope plot
http://qb.cshl.edu/genomescope/genomescope2.0/analysis.php?code=nnC4CPmgLE3605rbyM7y
My data is Hifi and I used -x ccs . I would like to know if you have other recommendations for parameters regarding my species ? thanks.
-x ccs
The text was updated successfully, but these errors were encountered:
Try -x ccs first, if not good, try to increase -s from 0.5 to 0.7 or ?.
-s
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Do I need to polish the HIFI assembly with this ?
minimap2 -t16 -ax map-pb -r2k dbg.raw.fa reads.fa.gz | samtools sort -@4 >dbg.bam samtools view -F0x900 dbg.bam | ./wtpoa-cns -t 16 -d dbg.raw.fa -i - -fo dbg.cns.fa
Yes, polish it
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Hi I am working on a triploid species which is highly heterozygous, see genomescope plot
http://qb.cshl.edu/genomescope/genomescope2.0/analysis.php?code=nnC4CPmgLE3605rbyM7y
My data is Hifi and I used
-x ccs
. I would like to know if you have other recommendations for parameters regarding my species ? thanks.The text was updated successfully, but these errors were encountered: