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PG-Seq Core Panel

PG-Seq™ Core Panel provides library preparation reagents and data analysis software for smooth implementation of PGT-M on Illumina® and Element Biosciences® sequencing platforms. This research panel analyzes 8 commonly targeted genes in monogenic disorders: BRCA1 & BRCA2, CFTR, DMD, HBB, F8, FMR1, GJB2.

For research use only. Not for use in diagnostic procedures.

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Feature	Specification
Product Group	PGTM Library Prep

For research use only. Not for use in diagnostic procedures.

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Product Variant

Unit Size: 24 rxns

Analysis

Included

Part #:

5340-0124

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Product information

Overview

The PG-Seq Core Panel analyzes over 200 SNPs located 2 Mb upstream and downstream of the gene or region of interest, covering a total of 4 Mb. Bioinformatics tools are employed to select SNPs with the highest probability of being informative. Additionally, full sequencing of the gene of interest is incorporated to facilitate direct analysis of the variants under study. Most of the pathogenic and likely pathogenic variants in splicing and UTR regions described on ClinVar are included.

Powered by Journey Genomics, the analysis software allows tracking of allele dropouts, recombination events and direct and indirect testing of common variants (SNV or indels) to determine embryo status. It also allows sex determination, analyzing SNPs in X and Y chromosomes, including variants in SRY gene.

Simultaneous screening of 8 frequently studied monogenic disorder genes
Enables tracking of allele dropout events
Generate dense SNP haplotyes
Easy to interpret software
Optimized for PG-seq Rapid kit v2 workflow

Additional product information

Figure 1: PG-Seq™ Rapid v2 includes all required reagents from cell lysis, whole genome amplification (WGA), indexing along with analysis software for automatic calling of aneuploidies and copy number variants. PG-Seq™ Core Panel uses as input WGA product from PG-Seq™ Rapid v2 or other kits, and includes all necessary reagents, barcodes and software for library preparation and automatic calling of variants. A single biopsy can be used for simultaneous PGT-A and PGT-M research.

Now you can schedule a one on one 30-minute online demonstration will cover everything you need to know about the analysis, powered by Journey Genomics, which is included with the PG-Seq Core Panel. During the demo, you will be able to see the analysis demonstrated and our experts will be able to answer any questions that you may have. The analysis software allows tracking of allele dropouts, recombination events and direct and indirect testing of common variants (SNV or indels) to determine embryo status. It also allows sex determination, analyzing SNPs in X and Y chromosomes, including variants in SRY gene. Please choose a timeframe that suits you best and we will provide you a Microsoft Teams personal link to join when the time comes. We look forward to speaking with you.