2013
DOI: 10.1038/nbt0613-565f
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Erratum: Corrigendum: Genome-wide mapping of methylated adenine residues in pathogenic Escherichia coli using single-molecule real-time sequencing

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Cited by 5 publications
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“…Whereas our first maNCB design worked well for the G A TC site, it could not differentiate m 6 A from A on the CTGC A G site , (Target Sets 3 and 4 in Table S3). Instead, t served as a good recognition nucleotide for NC probe to detect m 6 A on the CTGC A G sites (Figure S5 and S6).…”
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confidence: 94%
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“…Whereas our first maNCB design worked well for the G A TC site, it could not differentiate m 6 A from A on the CTGC A G site , (Target Sets 3 and 4 in Table S3). Instead, t served as a good recognition nucleotide for NC probe to detect m 6 A on the CTGC A G sites (Figure S5 and S6).…”
mentioning
confidence: 94%
“…This is partly due to the fact that detection of m 6 A at specific sites in a sequence is challenging. So far detection of N 6 -methyladenine in DNA has been demonstrated using a single-molecule, real-time sequencing method. , Detection of N 6 -methyladenosine in RNA has been shown using (1) nuclease cleavage followed by thin-layer chromatography (TLC) or mass spectrometry (MS), (2) immunocapturing of m 6 A-containing RNA fragments followed by sequencing, (3) ligation, and (4) a selective polymerase . However, these methods are laborious (e.g., require multiple steps to identify a single site), time-consuming (e.g., TLC and MS), and high-cost (e.g., enzymatic reaction).…”
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confidence: 99%