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Each panel consisted of 12 coded samples with various concentrations of inactivated, freeze-dried HSV type 1 (HSV-1), and HSV type 2 (HSV-2), or negative controls.
Each panel consisted of three (3) to five (5) panelists and a moderator.
Each panel consisted of raw EEG data and 3 qEEG tools: the color density spectral array (DSA), amplitude integrated EEG (aEEG) and the burst suppression rate (BSR).
Each panel consisted of the following qEEG tools, displayed separately for left and right hemisphere electrodes: rhythmicity spectrogram (rhythmic run detection and display; Persyst Inc), color density spectral array, EEG asymmetry index, and amplitude integrated EEG.
Each panel consisted of one general hospital physician (geriatrician), one general practitioner and one public health nurse.
Each panel consisted of 20 mice and each mouse received 20 μl of homogenate intracerebrally and 100 μl intraperitonially.
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Each panel consists of three members—usually a lawyer or a judge, a doctor, and a psychologist or a social worker.
Each panel consists of three members — usually a lawyer or a judge, a doctor, and a psychologist or a social worker.
Each panel consists of four sequential snapshots (top), a figure showing the heights of the indicated peaks (middle), and the half helical pitches between the indicated peaks (bottom).
Each panel consists of 84 cell cycles and apoptosis related assays along with seven human reference genes (ACTB, β2M, GAPDH, HPRT1, RPL13A, 18S, and YWHAZ).
Each panel consists of 26 blinded-duplicate (bovine) faecal samples, with one sample identified as a positive control, and includes designated critical-pass positive and negative samples along with samples spiked with mycobacterial species other than MAP.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com