NGS
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NGSgo®-ProntoFLX |
 Whole-gene amplification Compatible with ONT devices Available as RUO |
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NGS-Pronto® |
Amplification & barcoded library preparation DNA to results < 8h Up to 96 samples per run |
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NGS-Turbo® |
Amplification & library preparation DNA to results ~2.5h 1 sample per run |
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NGSgo-MX11-3 CE-IVD |
Multiplex amplification Whole-gene coverage RUO & CE-IVD (IVDR) |
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NGSgo-MX6-1 CE-IVD |
One-Day-Workflow 6 loci in 1 tube RUO & CE-IVD (IVDR) |
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NGSgo-AmpX v2 CE-IVD |
Optimized version of AmpX Single loci RUO & CE-IVD (IVDR) |
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NGSgo-AmpX v3 CE-IVD |
Optimized version of AmpX Single loci RUO & CE-IVD (IVDR) |
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NGSgo-Library Full Kit CE-IVD |
Complete solution for library preparation Includes NGSgo-LibrX, NGSgo-IndX plate & GenDx-AMPure XP beads RUO & CE-IVD (IVDR) |
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AlloSeq cfDNA |
Sample-to-report results in up to 24 hours with up to 1.5 hours hands-on time Minimally invasive blood test to measure dd-cfDNA Decentralized testing with no prior genotyping required |
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AlloSeq HCT |
A NGS based chimerism testing solution that is able to determine the relative contribution of up to 3 genomes in a single sample. A kit based test that offers high quality data with a recommended input of 10 ng of gDNA and up to 96 samples per batch. One-step multiplex assay that utilizes 202 SNPs across all autosomal chromosomes to differentiate between recipient and donor(s) gDNA |
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AlloSeq Tx |
Expandable gene content without impacting laboratory workflow Easy single-tube workflow with early indexing Reliable performance from lower-quality samples with reduced risk of allele dropout |
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