Next-generation sequencing of short reads is a powerful tool that has enabled advances in a wide variety of applications, including detection and quantification of RNA in biological samples, cfDNA fragment detection and counting, high-throughput NGS barcode sequencing, CRISPR screens, single-cell analysis, proteomics, and others. Short-read NGS is typically performed with one set of single-end or paired-end reads on a single flow cell.
This poster from Singular Genomics introduces the Max Read sequencing kit for the G4 Sequencing Platform, which enables multiple sets of independent single-end or paired-end reads on the same flow cell for a higher output of short reads without a significant impact on read quality.
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