Next Generation Sequencing services
Whole genome and whole exome sequencing, RNA-seq and single molecule sequencing.
A global network of CLIA/CAP certified laboratories which follow rigorous quality control methods. Our high-tech, automated laboratories, combined with our expert staff, generate high quality data, rapidly.
SeqPlus is our proprietary formalin-fixed paraffin-embedded (FFPE) whole genome and whole exome sequencing workflow which includes DNA isolation through secondary analysis. This method generates high molecular weight DNA molecules and achieves equivalent quality and coverage data to fresh-frozen tissue samples.Learn more
Secondary analysis on NGS data, including FASTQ quality, alignment, and variant calling. Our highly skilled bioinformatics team have developed and validated multiple pipelines that provide scalability and consistency for analyzing your genomic data.
Tertiary analysis including clinical interpretation (see Sequence Miner), QC analysis for sample/variant missingness, cohort analysis, and functional enrichment using GOseq and nGO seq. Our DeepCODE software accelerates new discovery research/validation, biomarker identification or responders v/s non-responders.Learn more
Your results can be delivered to the cloud via FTP, by disc in BAM or VCF format. We partner with Google Cloud, AWS, Microsoft Azure, NetApp, and Alibaba for all your cloud needs.