Once Can Be Enough by Allan Franklin & Ronald Laymon
Author:Allan Franklin & Ronald Laymon
Language: eng
Format: epub
ISBN: 9783030625658
Publisher: Springer International Publishing
5.3 âToo Good to Be Trueâ
In 1936 R.A. Fisher, the distinguished British geneticist and statistician, reanalyzed Mendelâs data and concluded, on the basis of Ï2 analysis, that Mendelâs data fit his hypotheses too well (Fisher 1936). They were âtoo good to be true.â Fisher obtained a value of Ï2â=â41.6056 for Mendelâs 84 experiments. A fit this good between data and theory has a probability of 0.00007, a highly unlikely event. Given his admiration for Mendelâs work, Fischer suggested that Mendelâs data had been falsified by a well-intentioned, unnamed assistant. Fisherâs Ï2 analysis, however, attracted little attention until around 1965, the centenary of the publication of Mendelâs paper. This led to an avalanche of commentary that has been extensively reviewed in Franklin et al. (2008, pp. 1â77) which also contains reprints of several of the most important papers in that deluge.
Here we will focus attention on what we consider in retrospect to be the most salient responses to Fischerâs conclusion that Mendelâs data were âtoo good to be true.â We do this to indicate in a telling and concise manner the nature of the problems with systematic uncertainty and possible confounding causes that Mendelâin large part unknowinglyâhad to deal with. Once Mendelâs work had been rediscovered these problems would in turn provide an ongoing challenge for the development of the science of genetics.
In short, there are two basic approaches to dealing with what has become known as the Mendelian Paradox, that is, the conflict between Mendelâs beautifully conceived experimental scheme and the surprising agreement between his data and his hypotheses. First, that Mendel somehow, perhaps unknowingly and inadvertently, biased his experimental procedures by improperly culling suspect progeny from his test samples. Second, that the expression of the Mendelian factors was corrupted by confounding causes which meant that Mendelâs experimental samples were not extracted from a population where those factors satisfied the binomial distribution. In other words, Fisherâs Ï2 analysis was inapplicable because Mendelâs peas were either not independently distributed within self-fertilizing pods or because of some confounding cause were not randomly expressed.
We begin our review with the second approach because, in the present context, it best sets the stage for a consideration of the first approach. Teddy Seidenfeld considered such a confounding process based on what he refers to as the Correlated Pollen Model15:Suppose that within the pea-flower for hybrids, 10 egg cells form according an i.i.d. [independent and identically distributed] âfairâ (binomial) distribution. However, approximating the speculated, checkerboard pattern that pollen have on the anther, suppose that exactly 5 of every 10 pollen cells arriving at the egg cells are dominant. Last, assume that, with equal probability, 2 of these 10 zygotes spontaneously abort, leaving 8 peas/pod. The result is a model where pollen cells are negatively correlated within a pod (Seidenfeld in Franklin et al. (2008, p. 233).
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