Case Reports in Genetics

Case Report

Targeted Next-Generation Resequencing of Gene Identifies Novel Multiple Variants Pattern in Severe Hereditary Factor V Deficiency

Table 1

Summary of coverage for analyzed samples by next generation sequencing method.
SampleAverage target coverageTotal bases Total reads Mapped readsBottleneck score
Original proband DNA sample 547 583,280,200 5,832,802 4,964,887 31.81
Duplicate534 549,426,400 5,494,264 4,720,781 32.81