The RFU peak height depends on the amount of DNA being analyzed. When the amount of DNA is very low, then it can be difficult to separate a true low-level RFU peak from
signal noise or other technical
artifacts. As a result, many forensic DNA laboratories have set minimum RFU peak-height levels in
scoring the analysis of
alleles. There are no firm industry-wide rules for establishing minimum RFU threshold values. Each laboratory, in general, has established its own threshold levels as one aspect of its particular validation procedure. Many laboratories have established both lower and upper thresholds for data interpretation, as a window of minimum and maximum readings. Some threshold levels can be derived experimentally based on the equipment's known
signal-to-noise ratios, or a threshold can be defined to match published data or the manufacturer specifications. The company which sells the most widely used equipment for STR typing, Applied Biosystems, Inc. (ABI), has recommended a peak-height minimum of 150 RFU, advising how peaks below that level should be judged with caution. However, many forensic laboratories which have ABI systems have defined lower thresholds, often only 50 to 100 RFU, as determined by their own studies. Many different factors can affect a laboratory's choice of thresholds. For instance, there might be regulatory guidelines in specific jurisdictions. Also, different kinds of instruments vary in sensitivity (such as
slab gel instruments being less sensitive than
capillary electrophoresis (CE) instruments). Individual instruments, of a particular model type, have also been known to differ in performance (e.g., differences among various ABI 310 units, all of the same model). Capillary electrophoresis instruments generally provide better resolution compared gel-based systems, as well having better sensitivity. In addition, some laboratories have set different threshold standards depending on which instruments in the lab are used for an analysis. Setting an upper maximum threshold is critical when analyzing DNA data within high quantity samples. Samples with large amounts of amplified DNA will report high RFU levels that might oversaturate an instrument's sensitivity to measure the results. In such cases, an accurate measurement of the relative peak heights and/or areas might be unattainable. Oversaturation can be a problem when analyzing mixed samples. ==References==