The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901

The longhorned tick, Haemaphysalis longicornis, feeds upon a wide range of bird and mammalian hosts. Mammalian hosts include cattle, deer, sheep, goats, humans, and horses. This tick is known to transmit a number of pathogens causing tick-borne diseases, and was the vector of a recent serious outbre...

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Main Authors: Felix D. Guerrero, Kylie G. Bendele, Noushin Ghaffari, Joseph Guhlin, Kristene R. Gedye, Kevin E. Lawrence, Peter K. Dearden, Thomas W.R. Harrop, Allen C.G. Heath, Yanni Lun, Richard P. Metz, Pete Teel, Adalberto Perez de Leon, Patrick J. Biggs, William E. Pomroy, Charles D. Johnson, Philip D. Blood, Stanley E. Bellgard, Daniel M. Tompkins
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340919309576
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spelling doaj-e5112225802b48f2a79579debaef0c862020-11-24T21:56:33ZengElsevierData in Brief2352-34092019-12-0127The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901Felix D. Guerrero0Kylie G. Bendele1Noushin Ghaffari2Joseph Guhlin3Kristene R. Gedye4Kevin E. Lawrence5Peter K. Dearden6Thomas W.R. Harrop7Allen C.G. Heath8Yanni Lun9Richard P. Metz10Pete Teel11Adalberto Perez de Leon12Patrick J. Biggs13William E. Pomroy14Charles D. Johnson15Philip D. Blood16Stanley E. Bellgard17Daniel M. Tompkins18USDA-ARS Knipling-Bushland US Livestock Insects Research Laboratory, Kerrville, TX, USA; Corresponding author. USDA-ARS Knipling-Bushland US Livestock Insects Research Laboratory, 2700 Fredericksburg Rd., Kerrville, TX, USA.USDA-ARS Knipling-Bushland US Livestock Insects Research Laboratory, Kerrville, TX, USATexas A&M AgriLife, College Station, TX, USAGenomics Aotearoa and Biochemistry Department, University of Otago, Dunedin, New ZealandSchool of Veterinary Science, Massey University, Palmerston North, New ZealandSchool of Veterinary Science, Massey University, Palmerston North, New ZealandGenomics Aotearoa and Biochemistry Department, University of Otago, Dunedin, New ZealandGenomics Aotearoa and Biochemistry Department, University of Otago, Dunedin, New ZealandAgResearch Ltd., c/o Hopkirk Research Institute, Private Bag 11008, Palmerston North, 4442, New ZealandTexas A&M AgriLife, College Station, TX, USATexas A&M AgriLife, College Station, TX, USADepartment of Entomology, Texas A&M University, College Station, TX, USAUSDA-ARS Knipling-Bushland US Livestock Insects Research Laboratory, Kerrville, TX, USASchool of Veterinary Science, Massey University, Palmerston North, New Zealand; School of Fundamental Sciences, Massey University, Palmerston North, New ZealandSchool of Veterinary Science, Massey University, Palmerston North, New ZealandTexas A&M AgriLife, College Station, TX, USAPittsburgh Supercomputing Center, Carnegie Mellon University, Pittsburgh, PA, USAManaaki Whenua-Landcare Research, Auckland, New ZealandDepartment of Zoology, University of Otago, Dunedin, New ZealandThe longhorned tick, Haemaphysalis longicornis, feeds upon a wide range of bird and mammalian hosts. Mammalian hosts include cattle, deer, sheep, goats, humans, and horses. This tick is known to transmit a number of pathogens causing tick-borne diseases, and was the vector of a recent serious outbreak of oriental theileriosis in New Zealand. A New Zealand-USA consortium was established to sequence, assemble, and annotate the genome of this tick, using ticks obtained from New Zealand's North Island. In New Zealand, the tick is considered exclusively parthenogenetic and this trait was deemed useful for genome assembly. Very high molecular weight genomic DNA was sequenced on the Illumina HiSeq4000 and the long-read Pac Bio Sequel platforms. Twenty-eight SMRT cells produced a total of 21.3 million reads which were assembled with Canu on a reserved supercomputer node with access to 12 TB of RAM, running continuously for over 24 days. The final assembly dataset consisted of 34,211 contigs with an average contig length of 215,205 bp. The quality of the annotated genome was assessed by BUSCO analysis, an approach that provides quantitative measures for the quality of an assembled genome. Over 95% of the BUSCO gene set was found in the assembled genome. Only 48 of the 1066 BUSCO genes were missing and only 9 were present in a fragmented condition. The raw sequencing reads and the assembled contigs/scaffolds are archived at the National Center for Biotechnology Information. Keywords: Tick genome, Pac Bio de novo assembly, Genome annotation, Cattle tickhttp://www.sciencedirect.com/science/article/pii/S2352340919309576
collection DOAJ
language English
format Article
sources DOAJ
author Felix D. Guerrero
Kylie G. Bendele
Noushin Ghaffari
Joseph Guhlin
Kristene R. Gedye
Kevin E. Lawrence
Peter K. Dearden
Thomas W.R. Harrop
Allen C.G. Heath
Yanni Lun
Richard P. Metz
Pete Teel
Adalberto Perez de Leon
Patrick J. Biggs
William E. Pomroy
Charles D. Johnson
Philip D. Blood
Stanley E. Bellgard
Daniel M. Tompkins
spellingShingle Felix D. Guerrero
Kylie G. Bendele
Noushin Ghaffari
Joseph Guhlin
Kristene R. Gedye
Kevin E. Lawrence
Peter K. Dearden
Thomas W.R. Harrop
Allen C.G. Heath
Yanni Lun
Richard P. Metz
Pete Teel
Adalberto Perez de Leon
Patrick J. Biggs
William E. Pomroy
Charles D. Johnson
Philip D. Blood
Stanley E. Bellgard
Daniel M. Tompkins
The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
Data in Brief
author_facet Felix D. Guerrero
Kylie G. Bendele
Noushin Ghaffari
Joseph Guhlin
Kristene R. Gedye
Kevin E. Lawrence
Peter K. Dearden
Thomas W.R. Harrop
Allen C.G. Heath
Yanni Lun
Richard P. Metz
Pete Teel
Adalberto Perez de Leon
Patrick J. Biggs
William E. Pomroy
Charles D. Johnson
Philip D. Blood
Stanley E. Bellgard
Daniel M. Tompkins
author_sort Felix D. Guerrero
title The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
title_short The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
title_full The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
title_fullStr The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
title_full_unstemmed The Pacific Biosciences de novo assembled genome dataset from a parthenogenetic New Zealand wild population of the longhorned tick, Haemaphysalis longicornis Neumann, 1901
title_sort pacific biosciences de novo assembled genome dataset from a parthenogenetic new zealand wild population of the longhorned tick, haemaphysalis longicornis neumann, 1901
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2019-12-01
description The longhorned tick, Haemaphysalis longicornis, feeds upon a wide range of bird and mammalian hosts. Mammalian hosts include cattle, deer, sheep, goats, humans, and horses. This tick is known to transmit a number of pathogens causing tick-borne diseases, and was the vector of a recent serious outbreak of oriental theileriosis in New Zealand. A New Zealand-USA consortium was established to sequence, assemble, and annotate the genome of this tick, using ticks obtained from New Zealand's North Island. In New Zealand, the tick is considered exclusively parthenogenetic and this trait was deemed useful for genome assembly. Very high molecular weight genomic DNA was sequenced on the Illumina HiSeq4000 and the long-read Pac Bio Sequel platforms. Twenty-eight SMRT cells produced a total of 21.3 million reads which were assembled with Canu on a reserved supercomputer node with access to 12 TB of RAM, running continuously for over 24 days. The final assembly dataset consisted of 34,211 contigs with an average contig length of 215,205 bp. The quality of the annotated genome was assessed by BUSCO analysis, an approach that provides quantitative measures for the quality of an assembled genome. Over 95% of the BUSCO gene set was found in the assembled genome. Only 48 of the 1066 BUSCO genes were missing and only 9 were present in a fragmented condition. The raw sequencing reads and the assembled contigs/scaffolds are archived at the National Center for Biotechnology Information. Keywords: Tick genome, Pac Bio de novo assembly, Genome annotation, Cattle tick
url http://www.sciencedirect.com/science/article/pii/S2352340919309576
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