Author

Arthur C Rand

University of California, Santa Cruz

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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Assay:long-read sequencing· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Approach:benchmark study· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1

Frequent Co-Authors

Benedict PateniD· 2 shared Miten JainiD· 2 shared Aaron R. QuinlaniD· 1 shared Adam M. PhillippyiD· 1 shared Alexander DiltheyiD· 1 shared Andrew David BeggsiD· 1 shared Arang RhieiD· 1 shared Audrey Musselman-Brown· 1 shared

Activity by Year

2017-2018 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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2 shared papersGenomics

Benedict PatenORCID

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2 papers

Recent·Most cited

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

Miten Jain, Sergey Koren, Karen H. Miga, Josh Quick, Arthur C Rand, Thomas A. Sasani, John R. Tyson, Andrew David Beggs, Alexander Dilthey, Ian T. Fiddes, Sunir Malla, Hannah Marriott, Tom Nieto, Justin O’Grady, Hugh E. Olsen, , Matthew Loose

Nanopore-only sequencing of GM12878 across 39 MinION flowcells (91.2 Gb) yielded an assembly with NG50 ∼3 Mb; adding 5× ultra-long reads raised NG50 to 6.4 Mbp.

Nature Biotechnology · Jan 29, 2018Peer-reviewedGenomics✦ In-depth digest

Cytosine Variant Calling with High-throughput Nanopore Sequencing

Arthur C Rand, Miten Jain, Jordan Eizenga, Audrey Musselman-Brown, Hugh E Olsen, Mark Akeson, Benedict Paten

The paper presents a probabilistic method to detect and classify cytosine modifications using Oxford Nanopore MinION sequencing with high accuracy.

Nature Methods · Feb 20, 2017Peer-reviewedGenomics