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Transcriptome de novo assembly was performed using the assembling program Trinity (Grabherr et al. 2011).
The LbL assembly was performed with positively charged PANI NFs and negatively charged GO dispersion [67].
The cell assembly was performed under an argon atmosphere in a glove box (H2O < 10 ppm).
De novo assembly was performed for the delicate mapping of each sequence.
The cell assembly was performed in an argon-filled glove box.
The in vitro light-controlled assembly was performed by expressing and purifying SspB and BNAS in E. coli BL21 (DE3).
Spindle assembly was performed as described [44].
Spindle assembly was performed as described above.
Finishing assembly was performed in Seqman (DNASTAR, USA).
Genome assembly was performed by two alternative, complementary approaches.
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The FF self-assembly was performed in a quartz cell directly following the heating-cooling procedure.
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