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.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
Nanomedicine
Landing page for the dataset
Landningssida för datasetet
Karolinska Institutet