https://www.selleckchem.com/pr....oducts/srt2104-gsk22
To detect gene inversion in two pedigrees affected with Hemophilia A by using Nanopore sequencing technology. Peripheral blood samples were taken from members of the two pedigrees. Following extraction of genome DNA, genetic variants of the carriers were detected by Nanopore sequencing and subjected to bioinformatic analysis. Nanopore sequencing has identified the niece of the proband of the pedigree 1 as carrier of Hemophilia A Inv22, and the mother of the proband of the pedigree 2 as carrier of Hemophilia A Inv1, which was
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