04/15/2026
GTC’s deep sequencing (>2500 read depth on tissue and BM and >25,000 read depth on liquid biopsy) enables detection of low-frequency variants, fusions, and splice events that standard approaches may miss—delivering a more complete molecular picture.
The result: greater sensitivity, fewer false negatives, and higher confidence in every report—so you can make informed clinical decisions when it matters most.
Don't accept partial results!
https://genomictestingcooperative.com/genomic-tests/