Prenatal Testing

Increase diagnostic yield when it’s needed most

Harness the full range of genomic testing or pinpoint familial variants through targeted testing

Four STAT Testing Options

Diagnostic prenatal testing needs to be sensitive, comprehensive, and fast. Experience testing with unparalleled, uniform coverage and competitive turnaround times for STAT prenatal whole genome sequencing, whole exome sequencing, CNV testing, and targeted testing.

Sample Types

Genomic DNA from prenatal samples*
Cultured cell from prenatal samples*
Direct products of conception (POC)/fetal tissue
*Maternal sample required for genomic DNA and cultured cell samples types

Note: When ordering a Duo or Trio test, STAT turnaround times apply to proband. Parental reports typically result 7-10 days after proband.

STAT Prenatal Whole Genome Sequencing

Combines superior coverage of the exome (>99%) with uniform coverage across both coding and non-coding regions
Includes deep intronic and promoter variants, CNV detection, and diagnostic SMN1 copy number characterization
TAT 10-14 days
Proband, Duo, and Trio

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STAT Prenatal Whole Exome Sequencing

Extensive coverage of known disease-causing genes and coding regions
Includes select deep intronic and promoter variants and CNV detection
TAT 7-10 days
Proband, Duo, and Trio

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STAT Prenatal CNGnome® Test

Detects large copy number changes (CNV) (>25kb) and UPD throughout the genome
Greater resolution than traditional microarray using a hybridization- and probe-free analysis
TAT 10-12 days

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