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Galminas, I.

Publications and source records attributed to Galminas, I..

2 recordsLinked to original sources

NinjaSeq: programmable restriction enzyme-based sequencing library preparation with random access for DNA data storage

DNA data storage allows sequences to be defined without biological constraints, yet readout workflows still depend on generic end-repair/dA-tailing chemistry. We developed NinjaSeq, a type IIS restriction endonuclease library-preparation strategy that incorporates recognition sites into primer flanks, enabling digestion to generate adapter-compatible overhangs and eliminating the need for conventional end preparation. By combining this chemistry with constrained coding that excludes internal recognition motifs, NinjaSeq produced sequencing quality and decoding performance consistent with standard protocols while reducing reagent burden and simplifying processing, including compatibility with one-pot restriction-ligation. The same sequence-directed design also enables physical random access during library preparation: targeting file-specific flanking sites enriched a desired file from a mixed pool by about sixteen-fold in a proof-of-concept experiment. These results position NinjaSeq as a practical ONT readout approach for DNA data storage. HIGHLIGHTSO_LINinjaSeq replaces end-repair/dA-tailing with REases for nanopore sequencing C_LIO_LIConstrained encoding excludes recognition motifs to protect payloads from cleavage C_LIO_LINinjaSeq achieves decoding accuracy comparable to standard library preparation C_LIO_LIDesigning file-specific RRS enables random access during library preparation C_LI

molecular biology↗

High Performance protocol for ultra-short DNA sequencing using Oxford Nanopore Technology (ONT)

In recent years, Oxford Nanopore Technologies (ONT) has gained substantial attention across various domains of nucleic acids research, owing to its unique advantages over other sequencing platforms. Originally developed for long-read sequencing, ONT technology has evolved, with recent advancements enhancing its applicability beyond long reads to include short, synthetic DNA-based applications. However, sequencing short DNA fragments with nanopore technology often results in lower data quality, likely due to a lack of protocols optimised for these fragment sizes. To address this challenge, we refined the standard ONT library preparation protocol to improve its performance for ultra-short DNA targets. Utilising the same core reagents required for conventional ONT workflows, we introduced targeted alterations to enhance compatibility with shorter fragment lengths. We then benchmarked these adjustments against libraries prepared using the standard ONT protocol. Here, we present a comprehensive, step-by-step protocol that is accessible to researchers of varied technical expertise, facilitating high-quality sequencing of ultra-short DNA fragments. This protocol represents a significant improvement in sequencing quality for short DNA fragments using ONT technology, broadening the range of possible applications. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=167 SRC="FIGDIR/small/632410v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@1c99f4eorg.highwire.dtl.DTLVardef@1f9cf50org.highwire.dtl.DTLVardef@199c8acorg.highwire.dtl.DTLVardef@1459f48_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗