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Plasmid DNA was prepared using the Qiagen plasmid preparation protocol.
The remaining L2, L3, and L4 libraries were prepared with the standard sample preparation protocol.
The genomic library was prepared using TruSeq DNA sample preparation protocol.
LigPrep's ligand preparation protocol was used to prepare these natural compounds.
Structure files of both the ligands were prepared using LigPrep's ligand preparation protocol [ 43].
The samples were subsequently prepared according to a standardized preparation protocol, mentioned below.
Sensors were prepared according to the 'SURFE2R sensor preparation' protocol (Nanion's standard procedures) using their sensor prep A2 and B solutions.
Libraries were prepared with the Illumina TruSeq sRNA preparation protocol (Cat. no. RS-930-1012).
Libraries were prepared according to Illumina's HiSeq 2000 library preparation protocol (Illumina, San Diego, CA, USA).
Poly-A enriched mRNASeq libraries were prepared following Illumina's TruSeq Stranded mRNA LT library preparation protocol (Illumina Inc., San Diego, CA) using 1 µg of total RNA.
DNA samples were prepared for the GAII as described on the sample preparation protocol (Illumina).
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