Despite its success, current limitations of NGS systems include long analysis times, labor-intensive protocols, extensive sample batching requirements for cost-effective use, and limited choice in instrumentation. There is a need for new DNA sequencing platforms that combine high accuracy, speed, and flexible throughput to provide timely results and cost-effective operation for research and clinical applications.
This technical report from Singular Genomics presents whole-genome sequencing data of a reference human genome, cell line NA12878 from the CEPH Utah Reference collection, using the G4, a new NGS platform from Singular Genomics designed to enable accurate sequencing and faster results to advance the state of the art in clinical and basic research.
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