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Published on: August 3, 2018
Jeremy R Wang1, James Holt2, Leonard McMillan2
1Department of Genetics, University of North Carolina at Chapel Hill, CB 3280, 3144 Genome Sciences Building, 250 Bell Tower Dr, Chapel Hill, 27599, NC, USA. jeremy_wang@med.unc.edu.
This study introduces a novel hybrid method for correcting long read sequencing errors using short reads. The approach enhances genome assembly contiguity and throughput, making long read technologies more economically viable for complex genomes.
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