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Dear LRcaller team,
I am calling SV genotypes on a dataset of 20 individuals sequenced with ONT (~40X).
I am runing LRcaller in parallel on each chromosome.
LRcaller help indicates that 3 different aligners can be used : bwa, minimap2 or seqan.
Using seqan, works perfectly, but requires a substantial amount of computing time.
Would one of the other aligner be a solution if I am facing a computing time issue ?
Thank you in advance for your help.
Regards,
Thomas
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