PROJECT SUMMARY
Integrated genomic and transcriptomic analyses capture a wealth of information that can improve our
understanding of normal biological phenomena and disease. Combining DNA and RNA next-generation
sequencing (NGS) data from the same sample can improve predictive power of diagnostic and prognostic
assays. However, performing multiomic analyses is often not feasible due to limited sample availability or low
nucleic acid yields especially in single-cells and liquid biopsies. Extracellular nucleic acids derived from liquid
biopsies such as plasma, urine and cerebrospinal fluid are increasingly used for rapid and non-invasive disease
detection and treatment response monitoring in cancer and infectious diseases. An integrated protocol that
captures both DNA and RNA can be of tremendous value in liquid biopsy-based diagnostics by saving precious
clinical samples and reducing reagents requirement and sequencing costs.
Traditional NGS library preparation methods for DNA and RNA have some overlap in protocol and
typically utilize a common sequencing platform. However, these methods are cannot be adapted for
simultaneous library generation due to substrate and enzymatic limitations. In contrast, Claret Bioscience’s
innovative single-strand ligation approach facilitates direct library preparation from both RNA and DNA in three
simplified steps. The method also adds nucleic acid-specific molecular barcodes which enable in silico
deconvolution of DNA and RNA-derived sequences, making this method ideal for comprehensive NGS analyses.
In this proposal, we seek to develop and optimize a concomitant DNA and RNA NGS library preparation
protocol using a contrived mixture of fragmented human genomic DNA and yeast RNA along with spike-in
controls (which serve as “ground truth”) as input. We will perform a series of experiments to test the efficacy of
the protocol using a range of input amount and variable ratios of DNA and RNA to mimic the compositions
frequently encountered in clinical samples. We will evaluate the stringency of adapter ligation using the nucleic
acid-specific barcode and generate a user-friendly bioinformatic pipeline that will ultimately accompany the
assay, for easy bioinformatic extraction of genomic and transcriptomic data from a given library. To evaluate
protocol performance, we determine if the molecular, sequencing and mapping metrics of our method are
equivalent to the metrics obtained with individual library preparation protocols, for both DNA and RNA. Finally,
we will demonstrate biological utility of the method using our in-house repository of cell-free nucleic acids derived
from healthy plasma samples. Successful accomplishment of these aims will generate a robust assay that
simultaneously generates DNA and RNA NGS libraries within four hours. When combined with minimally
invasive liquid biopsy-based approaches, the combinatorial NGS assay described here can significantly reduce
financial and physical burden on the patient.
