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

Camilla L. C. Ip(Centre for Human Genetics), Matthew Loose(University of Nottingham), John R. Tyson(University of British Columbia), Mariateresa de Cesare(Centre for Human Genetics), Bonnie L. Brown(Virginia Commonwealth University), Miten Jain(University of California, Santa Cruz), Richard M. Leggett(Norwich Research Park), David Eccles(Malaghan Institute of Medical Research), Vadim Zalunin(European Bioinformatics Institute), John Urban(Brown University), Paolo Piazza(Centre for Human Genetics), Rory Bowden(Centre for Human Genetics), Benedict Paten(University of California, Santa Cruz), Solomon Mwaigwisya(University of East Anglia), Elizabeth M. Batty(Centre for Human Genetics), Jared T. Simpson(Ontario Institute for Cancer Research), Terrance P. Snutch(University of British Columbia), Ewan Birney(European Bioinformatics Institute), David Buck(Centre for Human Genetics), Sara Goodwin(Cold Spring Harbor Laboratory), Hans J. Jansen(ZF Screens (Netherlands)), Justin O’Grady(University of East Anglia), Hugh E. Olsen(University of California, Santa Cruz)
F1000Research
October 15, 2015
Cited by 341Open Access
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Abstract

The advent of a miniaturized DNA sequencing device with a high-throughput contextual sequencing capability embodies the next generation of large scale sequencing tools. The MinION™ Access Programme (MAP) was initiated by Oxford Nanopore Technologies™ in April 2014, giving public access to their USB-attached miniature sequencing device. The MinION Analysis and Reference Consortium (MARC) was formed by a subset of MAP participants, with the aim of evaluating and providing standard protocols and reference data to the community. Envisaged as a multi-phased project, this study provides the global community with the Phase 1 data from MARC, where the reproducibility of the performance of the MinION was evaluated at multiple sites. Five laboratories on two continents generated data using a control strain of Escherichia coli K-12, preparing and sequencing samples according to a revised ONT protocol. Here, we provide the details of the protocol used, along with a preliminary analysis of the characteristics of typical runs including the consistency, rate, volume and quality of data produced. Further analysis of the Phase 1 data presented here, and additional experiments in Phase 2 of E. coli from MARC are already underway to identify ways to improve and enhance MinION performance.


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