Z-factor

The Z-factor is a measure of statistical effect size. It has been proposed for use in high-throughput screening (where it is also known as Z-prime), and commonly written as Z' to judge whether the response in a particular assay is large enough to warrant further attention.

Background

In high-throughput screens, experimenters often compare a large number (hundreds of thousands to tens of millions) of single measurements of unknown samples to positive and negative control samples. The particular choice of experimental conditions and measurements is called an assay. Large screens are expensive in time and resources. Therefore, prior to starting a large screen, smaller test (or pilot) screens are used to assess the quality of an assay, in an attempt to predict if it would be useful in a high-throughput setting. The Z-factor is an attempt to quantify the suitability of a particular assay for use in a full-scale, high-throughput screen.

Definition

The Z-factor is defined in terms of four parameters: the means ($\mu$) and standard deviations ($\sigma$) of both the positive (p) and negative (n) controls ($\mu_p$, $\sigma_p$, and $\mu_n$, $\sigma_n$). Given these values, the Z-factor is defined as:

:$\text = 1 -$

In practice, the Z-factor is estimated from the sample means and sample standard deviations

:$\text = 1 -$

Interpretation

The following interpretations for the Z-factor are taken from:

Note that by the standards of many types of experiments, a zero Z-factor would suggest a large effect size, rather than a borderline useless result as suggested above. For example, if σ_p=σ_n=1, then μ_p=6 and μ_n=0 gives a zero Z-factor. But for normally-distributed data with these parameters, the probability that the positive control value would be less than the negative control value is less than 1 in 10⁵. Extreme conservatism is used in high throughput screening due to the large number of tests performed.

Limitations

The constant factor 3 in the definition of the Z-factor is motivated by the normal distribution, for which more than 99% of values occur within 3 standard deviations of the mean. If the data follow a strongly non-normal distribution, the reference points (e.g. the meaning of a negative value) may be misleading. Another issue is that the usual estimates of the mean and standard deviation are not robust; accordingly many users in the high-throughput screening community prefer the "Robust Z-prime" which substitutes the median for the mean and the median absolute deviation for the standard deviation. Extreme values (outliers) in either the positive or negative controls can adversely affect the Z-factor, potentially leading to an apparently unfavorable Z-factor even when the assay would perform well in actual screening
.
In addition, the application of the single Z-factor-based criterion to two or more positive controls with different strengths in the same assay will lead to misleading results
. The absolute sign in the Z-factor makes it inconvenient to derive the statistical inference of Z-factor mathematically

. A recently proposed statistical parameter, strictly standardized mean difference ( SSMD), can address these issues


. One estimate of SSMD is robust to outliers.

See also

* high-throughput screening
* SSMD
* Z-score or Standard score

References

Further reading

* Kraybill, B. (2005) "Quantitative Assay Evaluation and Optimization" (unpublished note)
* Zhang XHD (2011
"Optimal High-Throughput Screening: Practical Experimental Design and Data Analysis for Genome-scale RNAi Research, Cambridge University Press"

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Effect size
Biological techniques and tools
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