BGI VISTA™ Chromosome Sequencing

BGI VISTA™ Chromosome Sequencing

Introduction

BGI VISTA™ Chromosome Sequencing uses NGS based low coverage whole genome sequencing (WGS) to help detect chromosome abnormalities before or during pregnancy. Testing can be performed on a variety of different sample types.

The results obtained from testing can reduce a patient’s emotional burden and information from the results can improve the chances of a future successful pregnancy. If the chromosome abnormality in the fetus causes pregnancy loss, parents can usually be reassured that the chance of recurrence is low, and avoid a costly medical check-up.

  • SUITABLE FOR:

    Individuals from high disease risk populations or patients who want to understand if a
    chromosomal abnormality was a factor in a miscarriage

  • TA TIME:

    10-12 working days

  • SAMPLE:

    Abortion Tissue, Core Blood (Gestation week >12 weeks), Peripheral Blood, DNA and Amniotic Fluid.

  • TECHNOLOGY:

    Low coverage WGS

Why Choose BGI VISTA™ Chromosome Sequencing?

  • Fast
  • Accurate
  • Affordable

Workflow

Ordering BGI VISTA™ Chromosome Sequencing is easy.

  • STEP 1

    Physician orders test

  • STEP 2

    Blood or saliva sample collecte

  • STEP 3

    Sample shipped to BGI and analyzed

  • STEP 4

    Results sent to physician

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