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Nuclei were identified using TO-PRO-3 (Invitrogen).
Orthologous gene content was identified using blastp to identify reciprocal-best-hits in pair wise inferred proteome comparisons.
Orthologous genes between S. proteamaculans and S. symbiotica scaffolds or S. marcescens were identified using BlastP to identify BRHs.
Coding regions in culicines were identified using comparisons to the An.
CLL cells could be reliably identified using CD160FCA to a level of 10−4.
Previous multimodel imaging studies have defined regions of cortex identified using fMRI to constrain tractography algorithms.
Genesets were identified using a signal-to-noise metric.
Potential outliers were identified using a distance-to-model (DModX) plot.
Different sets of sensors are identified using these objectives to monitor the target at different times.
More than 20 species were identified and used to identify major reaction pathways.
IBD and asthma were identified using hospital diagnoses; antiasthma medication was also used to identify asthma.
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