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Fig. 2 | BMC Medical Genomics

Fig. 2

From: Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis

Fig. 2

PGT haplotype analysis in embryo 1 to 11. Left, embryo inheritance of paternal haplotype. Right, embryo inheritance of maternal haplotype. The x-axis represents the loci on chromosome 1. The red points represent the allele frequencies of haplotype informative alleles among plasma reads, haplotype A specific allele was drawn above x-axis, and haplotype B specific allele was drawn below x-axis. The black line represents the logarithmic values of the odd ratios of the inherited haplotype. The paternal haplotype A carries c.10740 + 7G > A variant (F0), the paternal haplotype B is wild type. The maternal haplotype A carries p.Ser2251Ter (M0), and the maternal haplotype B carries c.1144-2A > C variant (M1). The vertical dot line indicates the location of target variant

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BMC Medical Genomics

ISSN: 1755-8794

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