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PMID: 23185243 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Mind the gap: upgrading genomes with Pacific Biosciences RS long-read sequencing technology.

PloS one ·Vol. 7 ·No. 11 ·2012-00-00 ·Pages e47768

English AC, Richards S, Han Y, Wang M, Vee V, Qu J, Qin X, Muzny DM, Reid JG, Worley KC, Gibbs RA

Abstract

Many genomes have been sequenced to high-quality draft status using Sanger capillary electrophoresis and/or newer short-read sequence data and whole genome assembly techniques. However, even the best draft genomes contain gaps and other imperfections due to limitations in the input data and the techniques used to build draft assemblies. Sequencing biases, repetitive genomic features, genomic polymorphism, and other complicating factors all come together to make some regions difficult or impossible to assemble. Traditionally, draft genomes were upgraded to "phase 3 finished" status using time-consuming and expensive Sanger-based manual finishing processes. For more facile assembly and automated finishing of draft genomes, we present here an automated approach to finishing using long-reads from the Pacific Biosciences RS (PacBio) platform. Our algorithm and associated software tool, PBJelly, (publicly available at https://sourceforge.net/projects/pb-jelly/) automates the finishing process using long sequence reads in a reference-guided assembly process. PBJelly also provides "lift-over" co-ordinate tables to easily port existing annotations to the upgraded assembly. Using PBJelly and long PacBio reads, we upgraded the draft genome sequences of a simulated Drosophila melanogaster, the version 2 draft Drosophila pseudoobscura, an assembly of the Assemblathon 2.0 budgerigar dataset, and a preliminary assembly of the Sooty mangabey. With 24× mapped coverage of PacBio long-reads, we addressed 99% of gaps and were able to close 69% and improve 12% of all gaps in D. pseudoobscura. With 4× mapped coverage of PacBio long-reads we saw reads address 63% of gaps in our budgerigar assembly, of which 32% were closed and 63% improved. With 6.8× mapped coverage of mangabey PacBio long-reads we addressed 97% of gaps and closed 66% of addressed gaps and improved 19%. The accuracy of gap closure was validated by comparison to Sanger sequencing on gaps from the original D. pseudoobscura draft assembly and shown to be dependent on initial reference quality.

MeSH Terms
Animals Base Sequence Cercocebus atys/genetics Databases, Genetic Decision Making Drosophila/genetics Genome/genetics Melopsittacus/genetics Reproducibility of Results Sequence Analysis, DNA/methods Software
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
English Adam C
Department of Molecular and Human Genetics, Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA. [email protected]
Richards Stephen
Han Yi
Wang Min
Vee Vanesa
Qu Jiaxin
Qin Xiang
Muzny Donna M
Reid Jeffrey G
Worley Kim C
Gibbs Richard A
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Article Info
Journal
PloS one
Abbr.
PLoS One
ISSN
1932-6203
Published
2012-00-00
Epub
2012-00-21
Pages
e47768
Language
English
Region
United States
NLM ID
101285081
PMCID
PMC3504050
Subset
IM
Grants
NCRR NIH HHS · S10 RR026605 · United States
NHGRI NIH HHS · U54 HG003273 · United States
NCRR NIH HHS · 1S10RR026605-01 · United States
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