Thanks for the input.
Should unplaced scaffolds in reference genome be used to map newly sequenced genome
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.
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