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Widely used microarray and proven method for accurate, timely preimplantation genetic screening results.
Microarray to assay whole chromosome copy number imbalances and subchromosomal structural imbalances in polar bodies, blastomeres and blastocysts.
This BeadChip array is optimized for cytogenetic studies using formalin-fixed paraffin-embedded (FFPE) paired tumor-normal samples.
This 12-sample BeadChip array enables analysis of genetic and structural variation in the human genome, such as duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.
This genome-wide karyomapping microarray provides insight into the inheritance of single-gene defects by testing single cells from embryo biopsies.
This consortium-built array provides comprehensive coverage of cytogenetically relevant genes for congenital disorders and cancer research.
Whole-genome amplification of total DNA from a single embryonic cell, or a few embryonic cells, for use in the karyomapping assay protocol.
Used to generate a DNA template from single cells. Ideal for use with 24sure aneuploidy screening arrays or VeriSeq PGS applications.
Amplified genomic DNA recommended for use as part of the 24sure protocols when analyzing amplified DNA from a single cell or a few cells.
The TruSeq Amplicon - Cancer Panel is a highly multiplexed targeted resequencing assay for detecting somatic mutations.
This expert-defined sequencing panel targets 94 genes and 284 SNPs associated with a predisposition towards various cancers.
This kit provides researchers with a comprehensive, cost-effective solution for identifying causal variants implicated in inherited cardiac conditions (ICCs).
Unambiguous, phase-resolved HLA typing in a single assay using proven Illumina NGS technology and Assign analysis software.
TruSight Inherited Disease is a targeted sequencing panel that focuses on 552 genes associated with severe, recessive pediatric onset diseases.
The TruSight Myeloid Sequencing Panel targets variants associated with myeloid malignancies such as AML, MDS, MPN, CML, CMML, and JMML.
This panel focuses on exonic regions harboring disease-causing variants. Labs can perform commonly ordered molecular assays on-site with one assay.
Provides comprehensive gene fusion detection in formalin-fixed, paraffin-embedded (FFPE) and other cancer research samples.
Targeting 1385 cancer genes for gene expression, variant, and fusion detection studies in many RNA sample types including blood, bone marrow, and FFPE.
TruSight Rapid Capture all-in-one kits enable targeted sequencing library preparation and enrichment for up to 96 samples in only 1.5 days.
Focused sequencing panel to assess 15 genes that are commonly mutated in solid tumors in a single assay, with a simple, rapid workflow.
Comprehensive next-generation sequencing (NGS) assay that targets DNA and RNA variants from the same FFPE sample.
This targeted sequencing panel enables clinical researchers to identify low-frequency variation in solid tumors across 26 genes.
A fully validated next-generation sequencing solution for PGS, providing accurate results in aneuploidy screening and extending future opportunities.
Our clinical cancer research solutions deliver accurate genomic information, and enable labs to analyze multiple genes in a single test.
Illumina NGS and array technologies deliver fast, accurate information that can guide choices along the reproductive and genetic health journey.
These assays generate target-enriched cDNA libraries from RNA, even from FFPE samples, for cancer gene fusion studies using Illumina sequencing.