bioRxivCancer BiologyPreprint
Flap-enabled next-generation capture (FENGC): precision targeted single-molecule profiling of epigenetic heterogeneity, chromatin dynamics, and genetic variation
M. Zhou, N. H. Nabilsi, A. Wang, M.-P. L. Gauthier, K. O. Murray, H. Azari, W. S. Owens, J. R. B. Newman, F. J. Pardo-Palacios, A. Conesa, A. Riva, T. L. Clanton, B. A. Reynolds, P. Concannon, J. O. Brant, R. Bacher, M. P. Kladde
Abstract
Targeted sequencing is an increasingly sought technology. Available methods, however, are often costly and yield high proportions of off-target reads. Here, we present FENGC, a scalable, multiplexed method in which target sequences are assembled into 5' flaps for precise excision by flap endonuclease. Recovery of length-matched sequences, amplification with universal primers, and exonucleolytic removal of non-targeted genomic regions mitigate amplification biases and consistently yield [≥] 80% on-target sequencing. Furthermore, optimized sequential reagent addition and purifications minimize sample loss and facilitate rapid processing of sub-microgram quantities of DNA for detection of genetic variants and DNA methylation. Treatment of cultured human glioblastoma cells and primary murine monocytes with GC methyltransferase followed by FENGC and high-coverage enzymatic methyl sequencing provides single-molecule, long-read detection of differential endogenous CG methylation, dynamic nucleosome repositioning, and transcription factor binding. FENGC provides a versatile and cost-effective platform for targeted sequence enrichment for analysis of genetic and/or epigenetic heterogeneity.
- organism: human
- organism: mouse
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: variant calling
- research focus: chromatin & epigenetic regulation
- approach: experimental assay
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