Sequencing data of DNA nanostructures selected for uptake in cells

Selection of DNA nanostructures by cellular uptake studied by high throughput sequencing. We generated a library of DNA nanostructures folded from single-stranded genomes and sequenced the initial library on Oxford nanopore (ONT) and Illumina. The data from this is stored in the files:Initial_library_ONT.fastqInitial_library_Illumina_merged.assembled.fastqWe then performed repeated selection experiment in the cell lines HEK293T and RAW 264.7 combined with sequencing to monitor the process. The data from HEK293T round 4,6,8 and 10 sequenced on Oxford nanopore is stored in the files: HEK293_R4_ONT.fastqHEK293_R6_ONT.fastqHEK293_R8_ONT.fastqHEK293_R10_ONT.fastqThe data from RAW264.7 round 4,6,8 and 10 sequenced on Oxford nanopore is stored in the files: Raw_R4_ONT.fastqRaw_R6_ONT.fastqRaw_R8_ONT.fastqRaw_R10_ONT.fastqThe data from HEK293T round 5 and 10 sequenced on illumina is stored in the files: HEK293_R5_illumina_merged.assembled.fastqHEK293_R10_illumina_merged.assembled.fastqThe data from RAW264.7 round 5 and 10 sequenced on illumina is stored in the files: RAW_R5_Illumina_merged.assembled.fastqRAW_R10_Illumina_merged.assembled.fastq