2013
DOI: 10.1128/genomea.00655-13
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Complete Genome Sequence of the Arcobacter butzleri Cattle Isolate 7h1h

Abstract: Arcobacter butzleri strain 7h1h was isolated in the United Kingdom from the feces of a clinically healthy dairy cow. The genome of this isolate was sequenced to completion. Here, we present the annotation and analysis of the completed 7h1h genome, along with a comparison of this genome to the existing A. butzleri genomes.

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Cited by 18 publications
(21 citation statements)
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References 11 publications
(11 reference statements)
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“…First, for each genome, shotgun and paired-end 454 reads were assembled using the Roche Newbler assembler (v 2.6) into a single chromosomal scaffold. Each scaffold was closed into one contiguous sequence, using the 454 repeat contigs and the Perl script contig_extender3 ([ Merga et al 2013 ]; see also supplementary File S1 , Supplementary Material online); contig gaps/junctions within each scaffold were also validated using PCR amplification and Sanger sequencing. Second, Illumina HiSeq or MiSeq reads were assembled de novo within Newbler; these Illumina contigs were assembled into the 454 assembly within Seqman (v. 8.0.2) to validate all 454 base calls.…”
Section: Methodsmentioning
confidence: 99%
“…First, for each genome, shotgun and paired-end 454 reads were assembled using the Roche Newbler assembler (v 2.6) into a single chromosomal scaffold. Each scaffold was closed into one contiguous sequence, using the 454 repeat contigs and the Perl script contig_extender3 ([ Merga et al 2013 ]; see also supplementary File S1 , Supplementary Material online); contig gaps/junctions within each scaffold were also validated using PCR amplification and Sanger sequencing. Second, Illumina HiSeq or MiSeq reads were assembled de novo within Newbler; these Illumina contigs were assembled into the 454 assembly within Seqman (v. 8.0.2) to validate all 454 base calls.…”
Section: Methodsmentioning
confidence: 99%
“…Shotgun and paired-end 454 reads were assembled using the Roche Newbler assembler (v2.6) into one or two chromosomal scaffolds, providing draft genome sequences with a coverage of 35–136× ( table 1 ). Intrascaffold gaps were filled using the 454 repeat contigs and the Perl script contig_extender3 ( Merga et al 2013 ). Contig gaps were closed/validated using PCR amplification and Sanger sequencing, generating draft pseudomolecules for each genome.…”
Section: Methodsmentioning
confidence: 99%
“…The de novo large contigs and the contigs derived from the reference assembly were used to create a draft scaffold. The scaffold gaps were filled using the small-repeat de novo contigs and the Perl script Contig_extender3 ( 8 ). The final genomic sequences had coverages of 325× (RM3196) and 322× (RM3197).…”
Section: Genome Announcementmentioning
confidence: 99%