2017
Could nanopore sequencing help us improve genome assembly of Eudiplozoon nipponicum (Polyopisthocotylea, Diplozoidae)?
VOREL, Jiří, Marie JANKŮJOVÁ, Jan OPPELT, Filip PARDY, Pavel ROUDNICKÝ et. al.Základní údaje
Originální název
Could nanopore sequencing help us improve genome assembly of Eudiplozoon nipponicum (Polyopisthocotylea, Diplozoidae)?
Autoři
VOREL, Jiří (203 Česká republika, domácí), Marie JANKŮJOVÁ (203 Česká republika), Jan OPPELT (203 Česká republika), Filip PARDY (203 Česká republika), Pavel ROUDNICKÝ (203 Česká republika), Jana ILGOVÁ (703 Slovensko), Hana DVOŘÁKOVÁ (203 Česká republika), Lucie JEDLIČKOVÁ (203 Česká republika), Libor MIKEŠ (203 Česká republika), Dagmar JIRSOVÁ (203 Česká republika), Božena KOUBKOVÁ (203 Česká republika), Milan GELNAR (203 Česká republika) a Martin KAŠNÝ (203 Česká republika, garant)
Vydání
6th ECIP meeting - European Centre of Ichtyoparasitology, 2017
Další údaje
Jazyk
angličtina
Typ výsledku
Prezentace na konferencích
Obor
10600 1.6 Biological sciences
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Kód RIV
RIV/00216224:14310/17:00095265
Organizační jednotka
Přírodovědecká fakulta
ISBN
978-80-210-8799-6
Klíčová slova anglicky
NGS; nanopore; Monogenea; Eudiplozoon; nipponicum; genome
Změněno: 13. 12. 2017 14:53, Mgr. Jiří Vorel, Ph.D.
Anotace
V originále
Ectoparasitic flatworms from the family Diplozoidae (Platyhelminthes, Monogenea) represent a serious bloodfeeding fish pathogens. Until now, the running research has been focused mainly on morphological and phylogenetical characteristics of these worms and the information related to the biochemical and molecular nature of the physiological processes is rather sporadic. To this date only two monogenean genomes are deposited in public sequence databases. Genomes of Gyrodactylus salaris (Monopisthocotylea, Gyrodactylidae) and Protopolystoma xenopodis (Polyopisthocotylea, Polystomatidae). Therefore, we designed whole-genomic sequencing of selected monogenean representative - Eudiplozoon nipponicum Goto 1891, which was performed by three sequencing techniques. 454/Roche (Junior sequencing platform), Illumina (MiSeq and HiSeq sequencing platforms) and modern Oxford Nanopore technique (MinION sequencing platform). Using 454/Roche Junior and both Illumina sequencing platforms, 164,773,962 short raw reads were originally generated. After trimming of low quality reads (Trimmomatic v. 0.36) and removing contaminatinon - reads given by fish host (Cyprinus carpio), 130,741,241 reads were used for the draft of genome assembly. Finally, 766,162 scaffolds were generated in total length 1,322,576,402 base pairs (1.3 Gb). But most of assembled scaffolds were identified as a Spiroplasma sp. or Emticicia oligotrophica (bacterial contaminations), which could mean that significant number of E. nipponicum reads could be unintentionally filtered out and final scaffold is incomplete. For purpose to improve E. nipponicum genome draft, we have additionally included reads generated by modern third generation sequencing method – nanopore sequencing. The MinION platform is a small and portable, real time working, low-cost USB device, producing long-read (theoretically up to 250 Kb). 500 working channels produced 1,097,634 reads with length up to 198,101 base pairs.
Návaznosti
GBP505/12/G112, projekt VaV |
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