We sequenced embryos for aneuploidy screening, and also for control took one genomic DNA sample, previously known with normal karyotype. All the samples were amplified with SurePlex system. After NGS on MiSeq with VeriSeq kit, this sample with normal karyotype had a trisomy of chr19 (the profiles of embryos looked as they should look). Is it possible, that there might be any amplification errors due to wide regions of euchromatin in chr19, and VeriSeq with Miseq is not suitable for testing usual DNA from leukocytes?

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