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The sequence reads were assembled by using the Edena de novo short-reads assembler (Genomic Research Laboratory, Geneva, Switzerland).
Genomic contigs were generated and assembled by using the Newbler assembler software (Roche Diagnostics, Basel, Switzerland).
Genomic contigs were generated and assembled by using the Newbler assembler software (Additional file 2: Table S3).
Pryosequencing reads representing 130 Mb of data (ca. 20.4× coverage) were assembled by using the Newbler assembler version 1.1.03.24 (Roche) into 1276 contigs with an N50 contig size of 8455 bp.
The shotgun sequences were assembled by using the GS de novo assembler.
The FASC is assembled by using the binder-free Ni@CNT as both the negative and positive electrodes but aqueous alkaline solution as the electrolyte.
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Next a number of subsets of data were integrated and scaled and the minimum set of data with acceptable completeness was assembled by using images 1 600 (the first third of the data).
By intertwining two as-prepared RGO/Mn3O4-30 RGO/Mn3O4-30rid flexibleectrodes, flexible symmetric all-solid-state fiber supercapacitor was assembled by using PVA/hybridas the gel electrolyte.
Sequences were edited and assembled by using ContigExpress in the VectorNTI program suite (Invitrogen, Carlsbad, CA, USA).
The trimmed reads of the PE and MP libraries were assembled by using SOAPdenovo v1.05 with the default parameters.
The MERS-CoV related reads were extracted and asseMERS-CoV relatedeqMan softwareadsom the Lasergene 7.1.0 program (DNASTAR, Madison, wereUSA), rextractedin andrassembledenome.
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