The company that carried out the analysis flagged all classrooms that showed a number of wrong-to-right erasures exceeding three standard deviations from the mean.
In immunocytochemistry analysis, Flag-Runx2 was mainly expressed in the nuclei after Dox treatment, and upregulation of Flag-Runx2 occurred in about 50% of Dox-treated cells.
Thus, despite a relatively low false-positive rate for this data type (just over 15%), there were 50 papers where a false-positive 'Phenotypic analysis' flag was the only flag selected.
Using week 14 as a baseline, we expected 84 weekly visits, which in the CUSUM analysis flagged an alarm at week 26 and weeks 30 through the end of the study (week 38).
Our mass spectrometry analysis of Flag-VAPA, Flag-VAPB and endogenous VAPB immunoprecipitates also revealed three binding partners for VAPA and VAPB that appeared to be very abundant, especially in Flag immunoprecipitates.
To test for direct interactions between TAK1 and BMP-responsive Smad proteins, we performed a Flag pull down analysis with Flag-tagged Smad proteins and in vitro translated, S-labelled TAK1.
System call trace analysis dynamically flags anomalous system call behavior as potentially dangerous.
Expression data were filtered before pathway analysis by flags.
However, the analysis also flags mutations that do not reside within conserved domains, such as the G98E mutation, which is found in the region between the highly conserved MH1N and MH1C domains.
Subsequently, analysis of Flag IPs from HEK293 cells expressing Flag-FUS revealed increased association of FUS with XRCC1, LigIII, and PARP-1, but not with other BER proteins (APE1, TDP1, PNKP, or FEN-1) in GO-treated cells (Fig. 2a).
