Hugh E Olsen

发表

The Oxford Nanopore MinION: delivery of nanopore sequencing to the genomics community

Hugh E. Olsen, B. Paten, Miten Jain, 2016, Genome Biology.

Rapid discrimination among individual DNA hairpin molecules at single-nucleotide resolution using an ion channel

Hugh E. Olsen, D. Haussler, D. Deamer, 2001, Nature Biotechnology.

Nanopore sequencing and assembly of a human genome with ultra-long reads

Brent S. Pedersen, Ian T. Fiddes, Karen H. Miga, 2017, Nature Biotechnology.

Discrimination among individual Watson-Crick base pairs at the termini of single DNA hairpin molecules.

J. T. Rodgers, Hugh E. Olsen, D. Deamer, 2003, Nucleic acids research.

Nanopore long-read RNAseq reveals widespread transcriptional variation among the surface receptors of individual B cells

Hugh E. Olsen, C. Vollmers, R. DuBois, 2017, Nature Communications.

Nanopore native RNA sequencing of a human poly(A) transcriptome

Angela N. Brooks, Hugh E. Olsen, N. Loman, 2018, bioRxiv.

MinION Analysis and Reference Consortium: Phase 1 data release and analysis

David A. Eccles, Hugh E. Olsen, E. Birney, 2015, F1000Research.

Mapping DNA Methylation with High Throughput Nanopore Sequencing

Jordan M. Eizenga, Hugh E. Olsen, B. Paten, 2017, Nature Methods.

MinION Analysis and Reference Consortium: Phase 2 data release and analysis of R9.0 chemistry

Richard M Leggett, Ewan Birney, Vadim Zalunin, 2017, F1000Research.

MinION-based long-read sequencing and assembly extends the Caenorhabditis elegans reference genome

John R Tyson, Terrance P Snutch, Hugh E. Olsen, 2018, Genome research.

Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes

Sergey Koren, David Haussler, Joel Armstrong, 2020, Nature Biotechnology.

Nanopore Long-Read RNAseq Reveals Widespread Transcriptional Variation Among the Surface Receptors of Individual B cells

Mark Akeson, Charles Cole, E. Camilla Forsberg, 2017 .

Linear assembly of a human centromere on the Y chromosome

David Haussler, Benedict Paten, Mark Akeson, 2018, Nature Biotechnology.

Cytosine Variant Calling with High-throughput Nanopore Sequencing

Benedict Paten, Mark Akeson, Jordan M. Eizenga, 2016, bioRxiv.

Nanopore ReCappable sequencing maps SARS-CoV-2 5′ capping sites and provides new insights into the structure of sgRNAs

Hugh E. Olsen, E. Birney, L. Ettwiller, 2021, bioRxiv.

Improved data analysis for the MinION nanopore sequencer

Benedict Paten, Mark Akeson, Ian T. Fiddes, 2015, Nature Methods.

Linear Assembly of a Human Y Centromere using Nanopore Long Reads

Karen H. Miga, Hugh E. Olsen, D. Haussler, 2017, bioRxiv.

A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions

Hugh E. Olsen, J. Gécz, A. Sharp, 2020, bioRxiv.

A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.

J. Gécz, A. Sharp, B. Paten, 2020, American journal of human genetics.

Identification of high-confidence human poly(A) RNA isoform scaffolds using nanopore sequencing

Hugh E. Olsen, M. Diekhans, L. Ettwiller, 2020, bioRxiv.