veriseq nipt v2
The new version expands the range of chromosomal and sub-chromosomal conditions associated with birth defects that laboratories can screen for. The BaseSpace RNA-Seq Alignment App analyzes data from the TruSight RNA Pan-Cancer Panel providing a simple results summary that includes a fusion table variant table and gene expression table.
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VeriSeq NIPT Solution v2 Package Insert Translated into.
. The VeriSeq NIPT Solution v2 is an in vitro diagnostic test intended for use as a screening test for the detection of genome-wide fetal genetic anomalies from maternal peripheral whole blood specimens in pregnant women of at least 10 weeks gestation. VeriSeq NIPT Solution v2 provides accurate information about fetal chromosomal status as early as 10 weeks of gestation using a single maternal blood draw. Each run including complete sample tracking is summarized in a downloadable report file.
View Options IVD Symbol Key Symbol key and translations for Illumina IVD products. VeriSeq NIPT Solution v2 Package Insert 1000000078751 v06 PDF 1 MB Aug 16 2021. Improved Q30 score support for UMIs extended shelf life and support for Illumina DNA PCR-Free Library Prep.
Intuitive Illumina Software Illuminas VeriSeq NIPT Workflow Manager Software includes a graphical interface to guide users through protocol selection and assay setup. ProductsLearnCompanySupportRecommended Links Products Software Analysis Services Popular Products Instruments Selection Tools. Claria NIPT based on Illumina VeriseqTM Solution v2 brings this whole-genome sequencing WGS approach to NIPT.
This product must not be used as the sole basis for diagnosis or other pregnancy management decisions. This CE-IVD software enables clinical labs in the EU to easily analyze sequencing data for noninvasive prenatal testing NIPT in their own lab. VeriSeq NIPT Solution v2 Consumables Equipment List Consumables and equipment list required for the VeriSeq NIPT Solution v2.
Improved Q30 score support for UMIs extended shelf life and support for Illumina DNA PCR-Free Library Prep. The integrated VeriSeq NIPT Solution v2 provides every - thing needed to run the assay. The assay provides information about fetal chromosomal status as early as 10.
PDF 1 MB Aug 13 2021. Percent Concordant XO XXX XXY XYY 9050 100 100 9170. This noninvasive test provides an option.
VeriSeq NIPT Solution v2 provides accurate information about fetal chromosomal status as early as 10 weeks of gestation using a single maternal blood draw. The BaseSpace RNA-Seq Alignment App analyzes data from the TruSight RNA Pan-Cancer Panel providing. VeriSeq NIPT Solution Comprehensive and reliable NIPT solution Reagents instruments and CE-IVD marked library prep and analysisreporting software in an automated workflow for in-lab prenatal aneuploidy screening.
The test offers an option to request the reporting of sex chromosome aneuploidy SCA. Business Wire Illumina has collaborated with Next Generation Genomic NGG Thailand to introduce an automated in-lab IVD solution called VeriSeq NIPT Solution v2 in Thailand. The CE-IVD VeriSeq NIPT Solution v2 is now registered for use in Thailand Vietnam Singapore South Korea Australia New Zealand Israel.
You can also use your own pipeline for analysis. Sequencing of the full fetal genome provides a. VeriSeq NIPT Solution v2 provides accurate information about fetal chromosomal status as early as 10 weeks of gestation using a single maternal blood draw.
Concordance of VeriSeqTM v2 for detecting sex chromosome aneuploidies. VeriSeq NIPT Solution v2 uses whole-genome sequencing to detect partial duplications and deletions for all autosomes and aneuploidy status for all chromosomes. VeriSeq NIPT Solution v2 is a next-generation sequencing based method to noninvasive prenatal testing Illuminas VeriSeq NIPT Solution v2.
NovaSeq 6000 Reagent Kits v15. VeriSeq NIPT Solution v2. This noninvasive test provides an option to screen for aneuploidy in all autosomes chromosomes X Y and partial deletions and duplications greater than 7 Mb across the genome.
It still offers an automated next-generation sequencing-based workflow that can process up to 96 samples in about a day with PCR-free library preparation. Equipment Height Width Depth Weight VeriSeqOnsiteServerv2 438 cm 173 in 178 cm 7in 635 cm 25 in 259kg 57lbs VeriSeqNIPT MicrolabSTARwithAutoload 903 cm 356 in 199 cm 783 in 1006 cm 396 in 160kg 353lbs VeriSeqOnsiteServerv2PlacementRequirements PositiontheVeriSeqOnsiteServerv2toallowfor. NovaSeq 6000 Reagent Kits v15.
The integrated VeriSeq NIPT Solution v2 provides every - thing needed to run the assay. View Options IVD Symbol Key Symbol key and translations for Illumina IVD products. The clinical accuracy of the CE-IVD VeriSeq NIPT Solution v2 was confirmed by evaluating more than 2300 plasma samples from pregnant women with singleton and twin pregnancies undergoing prenatal.
The automated workflow easily scales to analyze 24 48 or 96 samples per run to allow for efficiency and flexibility in managing sample volumes. Run the RNA-Seq workflow FASTQ only on the MiSeq and stream the data to BaseSpace. VeriSeq NIPT Solution v2 Package Insert 200006957 v00 for Canada.
The laboratory can choose to run basic or ge- nome-wide screening by sample. VeriSeq NIPT Solution v2 Consumables Equipment List Consumables and equipment list required for the VeriSeq NIPT Solution v2. Illumina has launched the VeriSeq NIPT Solution v2 a CE-IVD next-generation sequencing-based approach to noninvasive prenatal testing.
View Options VeriSeq NIPT Solution v2 Software Guide Instructions for use of the software involved with the VeriSeq NIPT Solution v2. View Options VeriSeq NIPT Solution v2 Software Guide Instructions for use of the software involved with the VeriSeq NIPT Solution v2. The VeriSeq NIPT Solution v2 assay enables accurate identification of fetal aneuploidy allowing detection of genome-wide fetal chromosomal anomalies with high clinical sensitivities and specificities and a low assay failure rateClinical Trial Notification CTN identification number ID.
Like its predecessor the VeriSeq NIPT solution v2 provides information about trisomy 21 13 and 18 as well as some sex chromosome aneuploidy.
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