Entering edit mode
7.5 years ago
chevivien
▴
90
Hii,
Is it in order to map unplaced scaffolds in reference genome against newly sequenced genome when carrying out reference based assembly? Or it is just ok to use placed chromosomes e.g (ch1-chr29 basing on the number of chromosomes in ref genome) . The purpose of the analysis is to obtain BAM files for CNV detection.
of course some organisms with unplaced scoffolds have gff file containing annotation.
Thanks for the input.
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