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(→Datasets employed in this study)

(→Datasets employed in this study)

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-								We have conducted the both non-hybrid approaches: <span style="background-color:#D4F2CE;">hierarchical genome-assembly process ([[HGAP]]v2.0)</span> and <span style="background-color:#D4F2CE;">PBcR pipeline via self-correction ([[PBcR pipeline]])</span> to ''de novo'' assemble the PacBio long reads. The datasets used in the non-hybrid approach are composed of various SMRT cells, ranging from 4 to 17 XL-C2 SMRT cells (<span style="background-color:#D4F2CE;">D5-D8</span>), and  a single SMRT cell gathered with PacBio RS II system and P4-C2 chemistry (<span style="background-color:#D4F2CE;">D9</span>).
+								We have conducted the both non-hybrid approaches: <span style="background-color:#D4F2CE;">hierarchical genome-assembly process ([[HGAP]])</span> and <span style="background-color:#D4F2CE;">PBcR pipeline via self-correction ([[PBcR pipeline]])</span> to ''de novo'' assemble the PacBio long reads. The datasets used in the non-hybrid approach are composed of various SMRT cells, ranging from 4 to 17 XL-C2 SMRT cells (<span style="background-color:#D4F2CE;">D5-D8</span>), and  a single SMRT cell gathered with PacBio RS II system and P4-C2 chemistry (<span style="background-color:#D4F2CE;">D9</span>).
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