Development of circulating cell-free DNA reduced representation bisulfite sequencing for clinical methylomics diagnostics
Andries De KokeriD, Lennart RamaniD, Ruben Van PaemeliD, Malaïka Van der LindeniD, Sofie Van de VeldeiD, Paul van der LeestiD, Bram Van GaeveriD, Anxhela ZakaiD, Karim VermaeleniD, Ingel DemedtsiD, Veerle SurmontiD, Ulrike Himpe, Franceska DedeurwaerdereiD, Liesbeth FerdinandeiD, Kathleen ClaesiD, Jilke De WildeiD, Mieke Zwager, Vincent D. de Jager, T. Jeroen N. HiltermanniD, Bram De WildeiD, Björn MenteniD, Katleen De PreteriD, Ed M. D. SchuuringiD, Jo Van DorpeiD, Nico CallewaertiD
Abstract
Methylation profiling of circulating cell-free DNA (cfDNA) is of great interest as a liquid biopsy assay for the detection and monitoring of cancer and other pathologies. Here we describe circulating cell-free DNA reduced representation bisulfite sequencing (cf-RRBS), enabling the use of highly effective RRBS on fragmented plasma cfDNA. This method enriches the CpG-rich RRBS target regions by enzymatic degradation of all off-target DNA rather than by targeted capture, in contrast to previous methods. Critical steps are fully enzymatic in a single-tube, making it rapid, cost-effective, robust, and easily implemented on a liquid-handling station for high-throughput sample preparation. We benchmark cf-RRBS results to those obtained by previous more complex methods and exemplify its use for accurate non-invasive subtyping of lung cancer, a frequent onco-pathology task. cf-RRBS enables any molecular pathology lab to tap into the cfDNA methylome, only making use of off-the-shelf reagents and open-source data analysis tools. One Sentence SummaryNovel methodology enables facile and cost-effective methylation profiling of fragmented plasma DNA, allowing for routine liquid biopsy clinical diagnostics, exemplified here for differential diagnosis of lung cancer subtypes.
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