Results comparable to fresh frozen
Generates sequence alignments covering 98% of the genome at a depth of 20x or greater, when sequenced at a depth of 70x for whole genome sequencing.
Unlock new insights from tumor samples with 98% sequence alignments covered at a depth of 20x. This process produces reliable, high-quality results for whole genome, exome, or multi-omic analysis comparable to fresh frozen-derived data, enabling quality mutation and copy number variation analyses.
Generates sequence alignments covering 98% of the genome at a depth of 20x or greater, when sequenced at a depth of 70x for whole genome sequencing.
Unlike traditional FFPE sequencing processes, ours can isolate enough high-quality DNA to achieve good coverage across whole genome or whole exome sequencing.
Allows for high quality mutation and copy number variation analysis.
In addition to pathology, you can now add whole genome and whole exome sequencing to your work flow.
Our assay works with archival tissue biobank samples as old as 15 years, routine clinical processing of samples for clinical trial recruitment, and tissue sections as part of normal clinical diagnostic workflows.
Our proprietary FFPE process can work on specimens with degraded DNA, cross-linked nucleic acids, and low quantities of material.
WuXi NextCODE offers access to Illumina's TruSightTM Oncology 500 (TSO 500).
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Hear Shannon Bailey present the results from a large cancer sequencing project where WuXi NextCODE's method was used to generate high-quality WGS data from FFPE tumor-normal sample pairs.
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Isolating sufficient quality DNA from samples is a major challenge in genomic research. Setbacks can raise costs, cause delays, and lead to failed studies. A new process from WuXi NextCODE, SeqPlus, offers time and cost savings with excellent results. SeqPlus greatly improves DNA extraction from formalin-fixed, paraffin-embedded samples.
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Our team has developed the WuXi NextCODE SeqPlus FFPE extraction method, which provides substantially improved coverage compared to traditional methods and even approximates the results obtained with fresh frozen samples at 10X depth, with similar numbers of heterozygous and homozygous calls.
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