BGI VISTA™ PGS

BGI VISTA™ PGS

Introduction

Preimplantation genetic screening (PGS) evaluates embryos for extra or missing chromosomes. PGS is an option for any in vitro fertilization (IVF) patient.

BGI VISTA™  PGS is used in conjunction with an IVF cycle. Embryos remain on-site at the patient’s IVF center. Cells are removed from an embryo and sent to BGI for genetic analysis.

BGI VISTA™  PGS can improve the chance of a successful pregnancy while reducing the chance of miscarriage or of having a child with a chromosome condition.

Who should consider BGI VISTA™ PGS?

Any Individual or couple undergoing IVF, especially those with the following indications:

  • Advanced maternal age (AMA);
  • Individuals/couples who have suffered repeated implantation failure (RIF);
  • Individuals/couples who have suffered repeated miscarriage (RM);
  • Severe male factor infertility;
  • Individuals/couples who are carriers of chromosomal abnormalities or have given birth to a child with chromosomal abnormalities.
  • SAMPLE:

    DNA from blastocyst cells (Recommended);
    Blastocyst cells (Frozen)

  • TA TIME

    10 working days

  • TECHNOLOGY:

    Low coverage WGS

Why Choose BGI VISTA™ PGS?

  • Comprehensive – covers all 24 chromosomes and can detect Aneuploidy/Structural Aberrations
  • Accurate –  99.9% accuracy with NGS
  • Affordable – one of the lowest price with high qualities in market

Workflow

Ordering BGI VISTA™ PGS is easy.

  • STEP 1

    Physician orders test

  • STEP 2

    Sample collection

  • STEP 3

    WGA & sequencing at BGI

  • STEP 4

    Results sent to physician

Learn more

Quick Contact