For context, please refer to the section Biological Information: Beyond the Reach of Chance (pages 10-12) in DNA by Design: An Inference to the Best Explanation for the Origin of Biological Information by Stephen C. Meyer.
I’ll quote two brief excerpts from this section (you can read the rest at the link above):
While many outside origin-of-life biology may still invoke “chance” as a causal explanation for the origin of biological information, few serious researchers still do.33 Since molecular biologists began to appreciate the sequence specificity of proteins and nucleic acids in the 1950s and 1960s, many calculations have been made to determine the probability of formulating functional proteins and nucleic acids at random. Various methods of calculating probabilities have been offered by Morowitz, Hoyle, Cairns-Smith, Prigogine, Yockey, and more recently, Robert Sauer.34 For the sake of argument, these calculations have generally assumed extremely favorable prebiotic conditions (whether realistic or not), much more time than was actually available on early Earth, and theoretically maximal reaction rates among the constituent monomers (i.e., the constituent parts of the proteins, DNA, and RNA). Such calculations have invariably shown that the probability of obtaining functionally sequenced biomacromolecules at random is, in Prigogine’s words, “vanishingly small . . . even on the scale of . . . billions of years.”35 As CairnsSmith wrote in 1971:
Blind chance . . . is very limited. Low-levels of cooperation he [blind chance] can produce exceedingly easily (the equivalent of letters and small words), but he becomes very quickly incompetent as the amount of organization increases. Very soon indeed long waiting periods and massive material resources become irrelevant. 36
More realistic calculations (taking into account the probable presence of nonproteineous amino acids, the need for specific functional proteins of considerable length, and the need for multiple proteins functioning in coordination) only reinforce these results. For example, recent theoretical and experimental work on the so-called “minimal complexity” required to sustain the simplest possible living organism suggests a lower bound of some 250 to 400 genes and their corresponding proteins.41 The nucleotide sequence space corresponding to such a system of proteins exceeds 4300000. The improbability corresponding to this measure of molecular complexity vastly exceeds the most conservative estimates of the so-called “universal probability bound” of 1 chance in 10150, the point at which appeals to chance become absurd given the “probabilistic resources” of the entire universe.42 Thus, when one considers the full complement of functional biomolecules required to maintain minimal cell function and vitality, one can see why chance-based theories of the origin of life have been abandoned. What Mora said in 1963 still holds:
Statistical considerations, probability, complexity, etc., followed to their logical implications suggest that the origin and continuance of life is not controlled by such principles. An admission of this is the use of a period of practically infinite time to obtain the derived result. Using such logic, however, we can prove anything.43
The main conclusion in this section is that, even under the most optimistic conditions, the probability of life originating by chance is so low that we can confidently infer chance was not the cause.
In other words, the argument moves from extreme improbability estimates to inferring impossibility.
Is this kind of inference ever justified, either in this specific context or in any other context?
NOTE: This is follow-up discussion to Are there any fallacies in arguments for design from DNA?