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In this study, we applied and benchmarked all currently available ONT library preparation methods to analyse RNAs in the prokaryotic model organism Escherichia coli K-12. These include direct sequencing of native RNAs, sequencing of native cDNAs, and sequencing of PCR-amplified cDNAs. Here, you find the basecalled and demultiplexed FASTQs and minimap2-mapped BAM files from untrimmed reads.
Nanopore, prokaryotes, RNA-seq
Nanopore, prokaryotes, RNA-seq
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