Fig. 1
Overview of the DNA data storage workflow. a The encoding process starts with mapping multiple digital files into 150-nucleotide DNA sequences and sending them for synthesis. Each file has unique sequence addresses at the 5′ and 3′ end of each oligonucleotide for random access retrieval. Using PCR primers containing complementary overhang sequences, a specific file can be amplified and concatenated into long double-stranded DNA molecules suited for ONT Nanopore sequencing. Upon sequencing, a subset of reads with high accuracy are used to decode the selected file. b Our assembly and decoding strategy enabled successful decoding of 1.67 MB of digital information stored in DNA using nanopore sequencing. Our work represents a 2-order of magnitude improvement in demonstrated decoding ability using nanopore sequencing for DNA storage. c Sequence-until diagram. Nanopore sequencing enables real-time coverage estimation for decoding of digital files store in DNA. This enables the user to generate reads until coverage is enough for successful decoding. Upon decoding, a different file can be sequenced in the same flowcell or the sequencing run can be stopped and resumed later on. d Four different files encoded in DNA were amplified, assembled and sequenced using ONT MinION platform. We implemented overlap-extension PCR and Gibson Assembly to build assemblies of 6, 10, or 24 fragments for each file
