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Times Cited: 197
Times Cited: 197
Times Cited
Times Co-cited
Similarity
Detecting DNA cytosine methylation using nanopore sequencing.
Jared T Simpson, Rachael E Workman, P C Zuzarte, Matei David, L J Dursi, Winston Timp. Nat Methods 2017
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Nanopore sequencing and assembly of a human genome with ultra-long reads.
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Detection of DNA base modifications by deep recurrent neural network on Oxford Nanopore sequencing data.
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Direct detection of DNA methylation during single-molecule, real-time sequencing.
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DeepSignal: detecting DNA methylation state from Nanopore sequencing reads using deep-learning.
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Nanopore native RNA sequencing of a human poly(A) transcriptome.
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A complete bacterial genome assembled de novo using only nanopore sequencing data.
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Performance of neural network basecalling tools for Oxford Nanopore sequencing.
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From squiggle to basepair: computational approaches for improving nanopore sequencing read accuracy.
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The Oxford Nanopore MinION: delivery of nanopore sequencing to the genomics community.
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Reading canonical and modified nucleobases in 16S ribosomal RNA using nanopore native RNA sequencing.
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Real-time, portable genome sequencing for Ebola surveillance.
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NanoMod: a computational tool to detect DNA modifications using Nanopore long-read sequencing data.
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Analysis of short tandem repeat expansions and their methylation state with nanopore sequencing.
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Accurate detection of complex structural variations using single-molecule sequencing.
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Direct RNA nanopore sequencing of full-length coronavirus genomes provides novel insights into structural variants and enables modification analysis.
Adrian Viehweger, Sebastian Krautwurst, Kevin Lamkiewicz, Ramakanth Madhugiri, John Ziebuhr, Martin Hölzer, Manja Marz. Genome Res 2019
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10
Bisulfite-free direct detection of 5-methylcytosine and 5-hydroxymethylcytosine at base resolution.
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10
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq.
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Decoding the epitranscriptional landscape from native RNA sequences.
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Assembly of long, error-prone reads using repeat graphs.
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Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
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Bismark: a flexible aligner and methylation caller for Bisulfite-Seq applications.
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The potential and challenges of nanopore sequencing.
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Human DNA methylomes at base resolution show widespread epigenomic differences.
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The diverse roles of DNA methylation in mammalian development and disease.
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Recent advances in the detection of base modifications using the Nanopore sequencer.
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Direct RNA sequencing enables m6A detection in endogenous transcript isoforms at base-specific resolution.
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Telomere-to-telomere assembly of a complete human X chromosome.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.