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Minion r9 flow cell

Manufactured by Illumina
Sourced in China

The MinION R9 flow cell is a key component of the MinION sequencing device, developed by Illumina. It is designed to enable real-time, long-read DNA sequencing. The flow cell contains nanopores that can detect and record the electrical signals generated as DNA passes through, allowing for the identification of the individual nucleotides.

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2 protocols using minion r9 flow cell

1

Comprehensive Genomic and Transcriptomic Profiling of MicroTom

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Fresh leaves of 4-week-old MicroTom that were grown in half-strength Murashige and Skoog basal medium with sucrose and Phytagel were collected, and the genomic DNA was sequenced on the Nanopore platform using a MinION R9 flow cell and the Illumina NovaSeq6000 platform with an insert size of 450 bp at Benagen (Wuhan, China).
Fresh tissues of roots, stems, leaves, flower, immature green fruits, and mature red fruits of plants grown in nutrient-rich soil were subjected to total RNA extraction using TRIzol (Invitrogen, Carlsbad, USA) according to the manufacturer’s protocol, and were used for subsequent RNA sequencing using different strategies. Samples from each tissue were subjected to construct a ribo-minus RNA library and small RNA library for RNA sequencing, whereas a mixture of the six samples was used to construction a PacBio SMRT library and a circular RNA library. The ribo-minus RNA libraries, small RNA libraries, and circular RNA library were sequenced using the Illumina HiSeq platform at Novogene Co., Ltd (Tianjin, China), and the PacBio SMRT library was sequenced using the PacBio Sequel System at Novogene Co., Ltd (Tianjin, China).
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2

Genome Sequencing of R. rhodochrous Strains

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Whole-genome sequencing of R. rhodochrous M8-35, M8-33 and M8-50 strains was carried out as described previously for R. rhodochrous M8 strain (Novikov et al., 2021 (link)). In brief, Illumina reads (obtained on Illumina MiSeq at NRC Kurchatov Institute, Moscow, Russia) and Nanopore reads (obtained on MinION R9 flow cell at Genotek, Moscow, Russia) were generated for each genome and used to obtain high-quality genome sequences. The genome of M8-35 strain consists of 6 149 108-nt circle chromosome and two linear contigs, 174 325-nt and 155 452-nt long, M8-33 genome consists of 6 148 942-nt circle chromosome and 121 763-nt linear contig, and M8-50 genome consists of 6 146 215-nt circle chromosome and 152 247-nt linear contig. Genomes sequences were deposited to NCBI Genbank under project numbers PRJNA989265 (strain M8-50), PRJNA989267 (M8-33), RJNA989179 (M8-35), and also available as Sequence 1-6 in the dataset (Grechishnikova et al., 2023 (link)). In order to trace the enzymes of nitrile-amide utilization pathway, genome annotations for M8-35, M8-33 and M8-50 were transferred from that of M8 strain using SnapGene® software (www.snapgene.com).
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