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新生兒

Reproductive & Genetic Health

白色背景

NIPT

VeriSeqTM NIPT Solution v2 - RUO

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Assess for autosomal aneuplodies, sex chromosome aneuploidies, deletions and duplications ≥7 Mb in size

Comprehensive view of the fetal genome

Highlights

Achieve reliable results with low failure rates in 26 hourse

Analyze 24, 48, or 96 samples per run with an easy-to-implement solution

Easy workflow with fast turnaround time

Scalable, semi-automated solution

PGT-A Solution

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About

Vitrolife is advancing science and human health by providing researchers with a new and powerful method of cellular analysis.

Magnetic levitation is the first truly novel approach to cellular analysis in 30 years. Extensive research has shown that cells of different types or states have unique physical signatures, levitating in predictable ways. 

Vitrolife Preimplantation Embryo Biopsy Solution: EmbryoMap

 

Introducing EmbryoMap from Vitrolife, a new streamlined workflow with advanced analytical features, designed by scientists, for scientists.  The EmbryoMap Solution has been analytically validated for detection of whole and sub-chromosomal imbalances with highly reproducible copy number, using cell line reference material and embryo biopsy samples. 

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Streamline Your Workflow Every Step of the Way

 
Samples are prepared for sequencing using the EmbryoMap Sample Prep Kit, sequenced on the Illumina MiSeq Sequencing System and run planning, data analysis and reporting performed using eMap software
 

EmbryoMap for labs assessing preimplantation embryo biopsy samples

 

Through evolution and innovation, the EmbryoMap solution has been analytically validated for detection of whole- and sub-chromosomal imbalances with highly reproducible copy-number, using cell line reference material and embryo biopsy samples

Samples are prepared for sequencing using the EmbryoMap Sample Prep Kit, sequenced on the Illumina MiSeq Sequencing System and data analysis and reporting performed using eMap software

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eMap Data Analysis

 
The cloud-based eMap software tool enables run planning, sample tracking, data analysis and reporting. The enhanced copy-number calling algorithm includes automated and manual calling options for full copy-number, sub-chromosomal and putative mosaic imbalances. Data can be visualised in a traditional CNV chart and new circos map. User-defined thresholds can be tailored to meet laboratory needs.

Ⓒ 2025 BY PRISMA BIOTECH. ALL RIGHTS RESERVED.

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