Genomic Profiling

Real-time NGS read scraping: reference sequence is compared base-by-base against the sample to call single-nucleotide variants and flag oncogenic mutations.

Sequencing Speed 40 bp/s

Mutation Rate 1.5%

Bases Scanned 0

Coverage 0.0x

Variants Called 0

Pathogenic 0

NGS

Variant Calling

Oncogenomics

Variant Call Log

Adenine (A)

Thymine (T)

Cytosine (C)

Guanine (G)

Pathogenic Variant