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Consequently, we employed immunoblot and quantitative sequence detection (QSD) assays to quantify UV-induced DNA damage.
After UV-C dose and outdoor microcosm experiments, irradiated oocysts were used for immunoblot and quantitative sequence detection (QSD) assays [28].
Because no quantitative sequence data (i.e. abundance of particular ITS types per location) were available for most locations, only a single sequence of each ITS type per country was included in the dataset.
Quantitative sequence variation among the predominant alleles of the apyrases of Phlebotomus species.
The choice of reference is critical because its effect on quantitative sequence analysis is non-negligible.
Quantitative sequence comparisons show that Apo-A-I, -A-IV, and E have evolved from a common ancestral gene [ 29].
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Quantitative sequence-cctivity Modeling.
Quantitative sequence-activity modeling.
Generally peptide descriptor sets obtained from the field of Quantitative Sequence-Activity Modeling (QSAM) are used in PCM [1, 11 15].
Moreover, most previous PCM modeling work uses the same descriptor set, the Z-scales published by Sandberg et al.[14], obtained from the field of Quantitative Sequence-Activity Modeling (QSAM) [1, 14 18].
The proposed method allowed quantitative sequence-specific detection of miR141 (with a detection limit of 1.03 pM) in a dynamic range from 1 pM to 10 μM, with an excellent ability to discriminate differences in miRNAs.
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