Sequencing data of DNA nanostructures selected for uptake in cells doi-10-17044-scilifelab-31323787-0 https://doi.org/10.17044/SCILIFELAB.31323787 Swedish National Data Service Svensk nationell datatjänst Landing page Sequencing data of DNA nanostructures selected for uptake in cells doi-10-17044-scilifelab-31323787-0 https://doi.org/10.17044/SCILIFELAB.31323787 Benson, Erik Rajwar, Anjali 2022-04147_VR Swedish National Data Service Svensk nationell datatjänst Landing page 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.fastq Initial_library_Illumina_merged.assembled.fastq We 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.fastq HEK293_R6_ONT.fastq HEK293_R8_ONT.fastq HEK293_R10_ONT.fastq The data from RAW264.7 round 4,6,8 and 10 sequenced on Oxford nanopore is stored in the files: Raw_R4_ONT.fastq Raw_R6_ONT.fastq Raw_R8_ONT.fastq Raw_R10_ONT.fastq The data from HEK293T round 5 and 10 sequenced on illumina is stored in the files: HEK293_R5_illumina_merged.assembled.fastq HEK293_R10_illumina_merged.assembled.fastq The data from RAW264.7 round 5 and 10 sequenced on illumina is stored in the files: RAW_R5_Illumina_merged.assembled.fastq RAW_R10_Illumina_merged.assembled.fastq Access to data through an external actor. Åtkomst till data via extern aktör.