VeriSeq PGS Kit- MiSeq

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15049007 RH-101-1001 VeriSeq PGS Kit – MiSeq (96 samples)
  • Description: All reagents required to prepare 96 samples for sequencing on the MiSeq sequencing system for the application of PGT-A (PGS). 2 x SurePlex DNA Amplification Systems (50 reactions per kit) 1 x VeriSeq PGS Library Preparation Kit – PGS (96 samples) 1 x VeriSeq Index Kit-PGS (24 indexes, sufficient for 95 samples) 4 x MiSeq Reagent Kit v3-PGS (upto 24 reactions per kit). This product is labeled for Research Use Only - Not for use in diagnostic procedures.
15049008 RH-102-1001 MiSeq Reagent Kit v3-PGS (24 samples)
  • Description: Reagents required for sequencing 24 prepared libraries on the MiSeq system 1 x MiSeq Reagent Kit v3-PGS (upto 24 reactions per kit). This product is labeled for Research Use Only - Not for use in diagnostic procedures.

Genomics by Vitrolife

Vitrolife now has exclusive distribution and development rights to Illumina’s preimplantation genetic testing business in EMEA and the Americas.

 

What is PGT-A?

PGT-A (Preimplantation Genetic Testing for Aneuploidy), formerly referred to as PGS (Preimplantation Genetic Screening) determines the chromosomal status of an in vitro embryo by screening all 23 chromosome pairs.

Aneuploidy can occur in any embryo; however, the chances increase with maternal age.3, 4

How does it work?

  1. Following ovarian stimulation and egg retrieval, a single or a few cells are biopsied from the embryo.
  2. Embryos are screened for aneuploidy
  3. Those most likely to be euploid (normal number of chromosomes) are either transferred to the uterus or frozen for future use
  4. The chances of IVF success are improved4, 6, 7

Advantages of PGT-A

Studies have shown that chromosomal aneuploidy in embryos is a cause of in vitro fertilization failure. PGT-A gives researchers a way to detect the chromosome number of an embryo to better understand how genomics impacts reproductive health.

PGT-A can be performed using next-generation sequencing (NGS) using the VeriSeq PGS Solution on the MiSeq Sequencing Instrument.

Make advancements with PGT-A

Using Illumina technology, the VeriSeq PGS solution can screen all 24 chromosomes in as little as 12 hours for an accurate, efficient view of the number of chromosomes in an embryo.

VeriSeq PGS kit - MiSeq

The VeriSeq PGS Kit - MiSeq uses NGS on the Illumina MiSeq System to screen all 24 chromosomes for aneuploidy in a single assay. The assay can be used on a single-cell (blastomere biopsy) or a few cells (blastocyst biopsy) from an embryo. The VeriSeq PGS workflow goes from sample to result in approximately 12 hours.

The VeriSeq PGS Kit is designed for multiplexing up to 24 samples per run on the MiSeq System. When 24 samples are not available for a run, it is possible to run the assay in a low-throughput, fast-run mode (8-12 samples/run).

 

Industry-leading

  • Industry-leading data quality: More than 90% of the world’s sequencing data is generated by Illumina sequencing by synthesis (SBS) chemistry*
  • Fast, streamlined workflow: Sample to answer in approximately 12 hours
  • High-throughput analysis: Screen up to 24 samples per run
  • Low input: NGS offers a highly sensitive method for screening embryos, requiring as little as 1 ng of DNA from a SurePlex DNA amplification reaction. DNA can be obtained from a blastomere biopsy, from a day 3 embryo, or from a trophectodermal (TE) biopsy from a blastocyst

*Data calculations on file. Illumina. Inc 2015

CNV profiles generated by BlueFuse Multi Software

Blastocyst biopsy sample showing aneuploidy for chromosomes 16 (Trisomy 16).

Blastocyst biopsy sample showing aneuploidy for chromosomes 7 (Monosomy 7) and 8 (Trisomy 8).

References

1. Centers for Disease Control and Prevention.Org Website Accessed March 11, 2016.
2. Scott RT, Ferry K, Su J, Tao X, Scott K, Treff NR. Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study. Fertil Steril. 2012;97(4):870-875.
3. Ata B, Kaplan B, Danzer H, et al. Array CGH analysis shows that aneuploidy is not related to the number of embryos generated. Reprod Biomed Online. 2012;24:614–620.
4. Harton GL, Munne S, Surrey M, et al. Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization. Fertil Steril. 2013;100(6):1695–1703
5. Yang Z, Liu J, Collins GS, Salem SA, Liu X, et al. (2012) Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis patients: results from a randomised pilot study. Mol Cytogenet 5: 24
6 Forman EJ, Hong KH, Ferry KM, et al. In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial. Fertil Steril. 2013;100(1):100–107.
7. Grifo JA, Hodes-Wertz B, Lee HL, Amperloquio E, Clarke-Williams M, Adler A. Single thawed euploid embryo transfer improves IVF pregnancy, miscarriage, and multiple gestation outcomes and has similar implantation rates as egg donation. J Assist Reprod Genet. 2013;30(2):259–264

8. Forman EJ, Hong KH, Ferry KM, Tao X, Taylor D, Levy B, Treff NR and Scott RT (2013) In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial. Fertility and Sterility 100 100–7.e1.

9. Rubio C, Bellver J, Rodrigo L, Castillón G, Guillén A, Vidal C, Giles J, Ferrando M, Cabanillas S, Remohí J et al. (2017) In vitro fertilization with preimplantation genetic diagnosis for aneuploidies in advanced maternal age: a randomized, controlled study. Fertility and Sterility 107 1122–1129.

10. Scott RT, Upham KM, Forman EJ, Hong KH, Scott KL, Taylor D, Tao X and Treff NR (2013) Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial. Fertility and Sterility 100 697–703.

11. Yang Z, Liu J, Collins GS, Salem SA, Liu X, Lyle SS, Peck AC, Sills ES and Salem RD (2012) Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study. Molecular Cytogenetics 5 24.

12. Gorodeckaja J, Neumann S, McCollin A, Ottolini CS, Wang J, Ahuja K, Handyside A and Summers M (2019) High implantation and clinical pregnancy rates with single vitrified-warmed blastocyst transfer and optional aneuploidy testing for all patients. Human Fertility (Cambridge, England) 1–12

13. Fiorentino F, Biricik A, Bono S, Spizzichino L, Cotroneo E, Cottone G, Kokocinkski F and Michel CM (2014) Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos. Fertility and Sterility Vol 101, Issue 5, Pages 1375-1382 e2. 

For Research Use Only. Not for use in diagnostic procedures.

Support

VeriSeq PGS Support Resources:
https://support.illumina.com/sequencing/sequencing_kits/veriseq-pgs-library-prep-kit.html

MiSeq Instrument MCS 3.1 + Local Run Manager (LRM) Software Updater Package Download:
https://support.illumina.com/sequencing/sequencing_instruments/miseq/downloads.html

Local Run Manager (LRM) & VeriSeq PGS Module Documentation:
https://support.illumina.com/sequencing/sequencing_software/local-run-manager/documentation.html

Local Run Manager (LRM) VeriSeq PGS Module Download:
https://support.illumina.com/sequencing/sequencing_software/local-run-manager/downloads.html

BlueFuse Workflow Manager (BWM) Software Documentation & Download (LRM can replace this):
https://support.illumina.com/sequencing/sequencing_software/bluefuse-workflow-manager.html

BlueFuse Multi (BFM) Software Documentation & Download:
https://support.illumina.com/array/array_software/bluefuse-multi-software.html

BlueFuse Multi (BFM) Annotation Database (BG_Annotation_Ens74_20160909.db):
https://support.illumina.com/downloads/bluefuse-multi-annotation-dbs.html

BlueFuse Multi Server
https://support.illumina.com/downloads/bluefuse-multi-server-download.html

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