Genome Check

GenomeCheck M (NIPT)

What is GenomeCheck M?

GenomeCheck M, the non-invasive prenatal testing (NIPT) service, is a screening for aneuploidy of a fetus with cell-free fetal DNA exists in the blood of a pregnant woman

Basic Information

  • Technology : NGS (Next Generation Sequencing)
  • Test Period : 10 ~ 24 weeks after pregnancy
  • Specimen : Maternal Blood or Maternal Plasma
  • Storage Condition : 2 ~ 8 ‘C (blood), -70 ‘C (plasma)
  • Transportation Condition : 2 ~ 8 ‘C (blood or plasma)

Key Features

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GenomeCheck G (Newborn Screening)

What is GenomeCheck G?

GenomeCheck G, is a newborn screening test to identify over 400 to 1,000 numerical and structural chromosomal abnormalities in newborns and infants.

Basic Information

  • Technology : CMA (Chromosomal Microarray Analysis)
  • Test Period : From birth onward
  • Specimen : Blood, Oral epithelial cell, Saliva
  • Storage Condition : 2 ~ 8 ‘C (blood), 15 ~ 30 ‘C (others)
  • Transportation Condition : 2 ~ 8 ‘C (blood), 15 ~ 30 ‘C (others)

Key Features

GenomeCheck K (Confirmatory Testing)

What is GenomeCheck K?

GenomeCheck K, is confirmatory testing for clients who have high risk in other GenomeCheck tests or for any people who wants to identify their genetic status

  • Minimizes genetic risks by identifying any fetal chromosomal abnormalities before birth.
  • Whole-genome testing for rare adults diseases enables early diagnosis and prevention of rare genetic conditions.
  • Preconception genome testing for couples assesses genetic risks during pregnancy by analyzing both partners’ genes.

Basic Information

  • Technology : Karyotype analysis + CMA
  • Test Period : For all pages
  • Specimen : Blood, Amniotic fluid, Chorionic villi
  • Storage Condition : 2 ~ 8 ‘C
  • Transportation Condition : 2 ~ 8 ‘C

Key Features

GenomeCheck PV (PGT)

What is GenomeCheck PV?

GenomeCheck PV is a pre-implantation genomic test (PGT) that identifies genetic abnormalities in embryos and selects normal embryos to enhance implantation.

Basic Information

  • Technology : NGS (Next Generation Sequencing)
  • Test Period : 3 ~ 5 days after fertilization
  • Specimen : Embryonic Cell (blastomere, part of trophectoderm)
  • Storage Condition : -25 ‘C ~ -15 ‘C
  • Transportation Condition : -25 ‘C ~ -15 ‘C

Key Features

GenomeCheck A (Cause of Miscarriage)

What is GenomeCheck A?

GenomeCheck A is a test to identify whether the client have a genetic disorders in the cause of repeated miscarriage using parental blood or aborted fetal tissue.

What is habitual miscarriage?

  • Occurs in approximately 1-5% of all women
  • If spontaneous miscarriage occurs three or more times in a row

Basic Information

  • Technology : DNA chip (CMA technology)
  • Test Period : After miscarriage
  • Specimen : Production of conception
  • Storage Condition : 2 ‘C ~ 8 ‘C
  • Transportation Condition : 2 ‘C ~ 8 ‘C

Key Features

GenomeCheck H (Cancer Screening)

What is GenomeCheck H?

GenomeCheck H is a Cancer Screening test analyzing various genetic markers to identify potential risks for 11 types of cancer (colorectal, lung, gastrointestinal, liver, thyroid, biliary tract/gallbladder, esophagus, pancreas, kidney, bladder, and breast cancer)

Basic Information

  • Technology : SNP Microarray (CMA technology)
  • Test Period : For all ages
  • Specimen : Blood, Oral epithelial cell
  • Storage Condition : 2 ‘C ~ 8 ‘C
  • Transportation Condition : 2 ‘C ~ 8 ‘C

Key Features