Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: Passed reads fastq

SRX14164088 fastqpassed Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: Passed reads fastq SRP359653 bp0 Viral dsRNA was denatured, polyA tailed, selected for polyA tails, and concentrated. The RNA was then prepared for Oxford Nanopore Direct RNA sequencing. Guppy 3.2.6 was used for basecalling. Using a subset of 44000 "passed" reads, genome segments were assembled using Canu v1.9. SRS11988260 Pseudomonas Phage ER16 fastqpassed OTHER GENOMIC Oligo-dT GridION SRX14164089 fast5passed Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: Passed reads fast5 SRP359653 bp0 Viral dsRNA was denatured, polyA tailed, selected for polyA tails, and concentrated. The RNA was then prepared for Oxford Nanopore Direct RNA sequencing. Guppy 3.2.6 was used for basecalling. Using a subset of 44000 "passed" reads, genome segments were assembled using Canu v1.9. SRS11988260 Pseudomonas Phage ER16 fast5passed OTHER GENOMIC Oligo-dT GridION SRX14164090 fast5failed Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: Failed reads fast5 SRP359653 bp0 Viral dsRNA was denatured, polyA tailed, selected for polyA tails, and concentrated. The RNA was then prepared for Oxford Nanopore Direct RNA sequencing. Guppy 3.2.6 was used for basecalling. Using a subset of 44000 "passed" reads, genome segments were assembled using Canu v1.9. SRS11988260 Pseudomonas Phage ER16 fast5failed OTHER GENOMIC Oligo-dT GridION SRX14164091 fast5skipped Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: Skipped reads fast5 SRP359653 bp0 Viral dsRNA was denatured, polyA tailed, selected for polyA tails, and concentrated. The RNA was then prepared for Oxford Nanopore Direct RNA sequencing. Guppy 3.2.6 was used for basecalling. Using a subset of 44000 "passed" reads, genome segments were assembled using Canu v1.9. SRS11988260 Pseudomonas Phage ER16 fast5skipped OTHER GENOMIC Oligo-dT GridION SRX14164092 fastqfailed Oxford Direct RNA Sequencing of Pseudomonas phage ERWIb: failed reads fast5 SRP359653 bp0 Viral dsRNA was denatured, polyA tailed, selected for polyA tails, and concentrated. The RNA was then prepared for Oxford Nanopore Direct RNA sequencing. Guppy 3.2.6 was used for basecalling. Using a subset of 44000 "passed" reads, genome segments were assembled using Canu v1.9. SRS11988260 Pseudomonas Phage ER16 fastqfailed OTHER GENOMIC Oligo-dT GridION