An improved assembly of the loblolly pine mega-genome using long-read single-molecule sequencing
Author(s) -
Aleksey V. Zimin,
Kristian Stevens,
Marc Crepeau,
Daniela Puiu,
Jill L. Wegrzyn,
James A. Yorke,
Charles H. Langley,
David B. Neale,
Steven L. Salzberg
Publication year - 2017
Publication title -
gigascience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.947
H-Index - 54
ISSN - 2047-217X
DOI - 10.1093/gigascience/giw016
Subject(s) - contig , sequence assembly , mega , loblolly pine , hybrid genome assembly , nanopore sequencing , genome size , deep sequencing , genome , computational biology , biology , computer science , pinus <genus> , genetics , gene , botany , transcriptome , gene expression , physics , astronomy
The 22-gigabase genome of loblolly pine (Pinus taeda) is one of the largest ever sequenced. The draft assembly published in 2014 was built entirely from short Illumina reads, with lengths ranging from 100 to 250 base pairs (bp). The assembly was quite fragmented, containing over 11 million contigs whose weighted average (N50) size was 8206 bp. To improve this result, we generated approximately 12-fold coverage in long reads using the Single Molecule Real Time sequencing technology developed at Pacific Biosciences. We assembled the long and short reads together using the MaSuRCA mega-reads assembly algorithm, which produced a substantially better assembly, P. taeda version 2.0. The new assembly has an N50 contig size of 25 361, more than three times as large as achieved in the original assembly, and an N50 scaffold size of 107 821, 61% larger than the previous assembly.
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