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Each library had its own rules.
Each library had a construction budget of $400,000.
cNumber of clones in each library.
About 60 positive clones were sequenced in each library.
Each library was sequenced independently.
Each library of P16S sequences were aligned using ClustalW.
Each library was sequenced in a single lane.
Control siRNAs were plated in duplicate in each library plate.
Contig lengths were then averaged independently for each library.
RNA pooling system was generated for each library.
Each library was indexed.
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