Test Order Form

Variantyx offers an end to end clinical service, from sample collection to diagnosis for rare genetic disorders. Our unique collaborative diagnostic approach combined with state-of-the-art technology ensures high diagnostic yield and fast turnaround time. Diagnosed by a US board certified molecular geneticist, fully insured, HIPAA, CLIA and CAP compliant.

 

Sequencing Option

Structural variant and CNV analysis

Coverage¹ in intronic / intergenic areas

Coverage¹ of all coding regions

Coverage¹ in genes of interest

Whole Genome²

Yes

~96.5%

~96.5%

~96.5%

Whole Exome³

No

N/A

95%

Varies

Panel

No

N/A

N/A

Full

¹Bases covered at 20X and higher
²Sequenced on Illumina HiSeq X Ten PCR-free at 30X
³Sequenced on Illumina HiSeq 2500/4000 at 100X on target with Agilent SureSelect V5
 

Use:

Cohort Size:

Other Cohort Size:
Sample or Tissue Type:

Other Sample or Tissue Type:
Sequencing Type:

Turnaround Time:

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