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For the reference modification, we used only origin reads the first five times and both origin and common reads the last five times.
For stable genetic modification, we used the self-inactivating HIV1-based lentiviral vector (LentiV) for transgene delivery in our study, which can integrate transgene into the host genome.
For the first modification, we used a crustal thickness of 10 km to the east of the Bonin ridge (Fig. 4) to match exactly the structure of line OGr1.
To determine whether tyrosine phosphorylation modulates O-GlcNAc modification we used biotinylated synthetic peptides with a phosphate group attached to Tyr114 and Tyr259 in in vitro O-GlcNAc assays.
For network modification, we used a nonlinear stochastic model and the Akaike Information Criterion AICC).
To maximize our chances for demonstrating SUMO modification, we used in-bacto system (see Materials and Methods) developed by the Courey Lab (Nie et al. 2009).
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In order to further verify the effectiveness of modification, we use DC-GR as reinforcement to enhance epoxy resin.
In order to further verify the effectiveness of modification, we use the obtained CNTs (PS-fCNTs) as reinforcement to enhance PS films.
By a slight modification, we use the methods and the framework of [3, 5] to prove Theorem 2.2.
For MYC ChIP-seq we used MACS2 (p-value < 1×10−6), while for histone modifications we used SICER V1.1 (window size = 200; gap size = 200; FDR < 0.01).
After HHT and the follow up modifications, we used MassSpecWavelet, SpecAlign, and PROcess for peak detection.
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