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Fig. 6 | BMC Medical Genomics

Fig. 6

From: ECNano: A cost-effective workflow for target enrichment sequencing and accurate variant calling on 4800 clinically significant genes using a single MinION flowcell

Fig. 6

Middle position showing the target variant(s) in 3 patient samples and the alignment of the adjacent positions: patient sample 1 (top) with homozygous C > T SNP in SLURP1; patient sample 2 (middle) with 10-base insertion in BCAP31; and patient sample 3 (bottom) with heterozygous C > T SNP in UROC1

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BMC Medical Genomics

ISSN: 1755-8794

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