• TOP
  • > Healthcare Providers > About PGT-A

    For Providers

    About PGT-A

    About PGT-A

    About our service

    The test is performed using approximately 5-10 cells obtained from a biopsy of the trophic ectoderm (TE) of a blastocyst on thet fifth day afterfertilization.
    The whole genome of the cell-derived human DNA is amplified and the increase or decrease in chromosome number is examined based on diploid/euploid chromosomes, which have two copies each.
    Depending on the specimen, mosaic aneuploidymay be detectedMosaic aneuploidy is a condition in which cells without chromosomal aneuploidy and cells with chromosomal aneuploidy are mixed in the analyzed fetal tissues. Mosaic aneuploidy may disappear as the fetus develops, but there is a risk that it may cause infertility, repeated implantation failure, or the birth of a child with birth defects, mental retardation or developmental disabilities.

    Features

    ・Specimens are transported by a specialized specimen transport company.
    ・Includes multiplicity analysis as the standard.
    ・KAT-Score, a comprehensive evaluation of the degree of mosaicism, is indicated.
    ・Notation of the embryo score, which is a combination of two evaluations; PGT-A results and the embryo grade

    If you are interested in our test, please contact our inquiry desk(info@varinos.com).
    ※This service is for research use only.

    Flow of PGT-A

    • 01

      Before making a request

      Please contact our sales representative.
      Our sales representative will explain the contract, inspection request, and additional necessary paperwork.

    • 02

      Order a test kit

      Please fill out the "PGT-A Kit Order Form" and fax it to us.
      The kit will be sent by frozen delivery.
      The kit includes a test request form, 0.2mL PCR tubes, 1% PVP-PBS solution (3 tubes), TubingBuffer (3 tubes), 96-well box and 96-well boxlabel, and specimen barcode labels(15 labels).

    • 03

      Specimen collection and packaging

      Please collect the specimen and package it according to our instructions.
      Please fill out the "Test Request Form" with the specimen information.

    • 04

      Delivery of specimens

      Please fill out the "Specimen Collection Request Form" and fax it to us.
      A representative from our affiliated specimen transport company will visit you to collect your specimen.

    • 05

      Report of test results

      We will perform DNA analysis and secondary data analysis using a next-generation sequencer at our laboratory, and return the test result report to you.
      The report will be sent to you within 10 business days from the date we receive your specimen. (Excluding Saturdays, Sundays, and national holidays)
      Please note that the delivery date may be delayed depending on the progress of the Japanese Society of Obstetrics and Gynecology's Committee for Evaluation of Analysis Results. Please be aware of this in advance.

    About the biopsy technique validation analysis

    Service Overview

    By amplifying the DNA of embryo biopsies and tubed specimens, we can objectively assess the success rate of embryo biopsies.

    Features

    ・Biopsy techniques can be confirmed using to-be discarded embryos or mouse embryos.
    ・Price is reasonable as a next generation sequencer is not used for genome analysis.

    Flow of biopsy technique validation analysis

    • 01

      Advance briefing

      The person in charge will explain the flow of the analysis.

    • 02

      Ordering a Kit

      Please order a kit using the order form.

    • 03

      Sample Shipping

      Please ship 5-10 cell biopsy samples that are frozen to our laboratory.

    • 04

      DNA extraction and confirmation

      The entire genome of the specimen is amplified by PCR, and the presence or absence of DNA is confirmed by measuring the DNA concentration along with electrophoresis.

    • 05

      Delivery

      The analysis results are delivered as a report (in principle, within 20 business days).