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Vol. 10, Issue 3, 273-274, March 2000
INSIGHT/OUTLOOK
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ARTICLE |
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The August 1999 issue of Genome Research
presented a very interesting editorial,
"Hypothesis-Limited Research," on the status and discovery function
of scientific hypotheses in disciplines generating large amounts of
data (Goodman 1999
). Dr. Goodman points to two types of limitations
generated by hypotheses
one theoretical and one pragmatic. She argues
that generating at least some type of data, for example, large-scale
sequencing, does not require hypotheses. From a practical point of
view, a hypothesis often complicates the scientific discovery flow,
generating a hypothesis is time consuming and biases data
interpretation. Consequently, Goodman urges giving up on proposing
theory first and collecting data afterward. She supports her suggestion
with historical examples, presenting great scientific discoveries that
were not based on a hypothesis, although contrary interpretation has
been presented by others (
astowski 1996
). Let us have a look at
how heretical Goodman's proposal is, if at all.
A Critique of Goodman's Standpoint
From Goodman's argumentation the conclusion can be drawn that molecular biology is the first experimental scientific discipline in which accumulation of data is so dynamic and fast that researchers cannot follow it by formulating an adequate number of hypotheses. This statement does not decrease the value of hypotheses in science but, as we will show here, it increases it.
From a methodological point of view, Goodman argues against a
hypothetical program of research (Popper 1959
). This program suggests
the following procedure of scientific discovery:
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Let us note that this is not a new idea; it resembles another scheme
that was suggested quite long ago. It belongs to the positivist
tradition of science and was developed within logical empiricism
(see Hempel 1966
). It can be presented as follows:
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In light of the juxtaposition of formula [G] and [P], the key methodological problem in Goodman's argument is the meaning of hypotheses and their role in scientific discovery. The question is how to reconcile the heuristic function of hypothesis with the demonstration of the hypothesis' correctness by identifying tests that falsify the hypothesis. If the test verifies the hypothesis, we assume that we can accept it as empirically justified.
Goodman suggests that the experimental data are a starting point in molecular biology research. This is true in many fields of science. Only in the next step do scientists propose hypotheses that then are checked by falsification tests. In this procedure hypotheses are based on "solid" facts and then in the empirical test undergo a falsification, not a verification This procedure is not described by scheme [H], in which a hypothesis is a starting point, nor by scheme [G] in which data are a starting point but facts verifying a hypothesis are a final result, nor by scheme [P] in which facts are both the alpha and omega point.
Consequently, a new problem appears, which we call the dilemma of scientific hypotheses' discovery validity [D]. The dilemma is formulated as follows: What is the role of a hypothesis' explanatory status in relation to the usage of observations (i.e., facts) in falsification of the hypothesis?
Proposed Solution to Dilemma [D]
This dilemma [D] cannot be solved within the philosophy
of science presented by Goodman. However, it can be addressed within the Idealization Theory of Science (ITS) (Nowak 1977
, 1981
). According to ITS, research in the experimental sciences proceeds according to the
following scheme:
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In contradiction to this, Goodman interprets scientific hypothesis quite narrowly, that is; as a conjectural description of empirical regularities in data. In this meaning of hypothesis, regardless of how numerous the accumulated facts, they always are interpreted as components of a hypothesis' positive test.
In light of [ITS] it is clear that (1) researchers do not have a single but, rather, many different descriptions of relations; (2) researchers, depending on their theoretical knowledge, can provide different descriptions (hypotheses); and (3) facts (experimental data) alone do not imply anything about their explanatory status. On the basis of their hypotheses, researchers decide how to relate them to the facts. Therefore, according to statements 1, 2, and 3, those theorized descriptions should be treated as theoretical filters for experimental data selection.
Consequently, we can conclude that in science, from a certain set of
possible theoretical descriptions (hypotheses) one is chosen that is
the most adequate according to objective criteria. How can one choose
the best hypothesis? Falsification criteria should be applied to all
competing hypotheses, and one that fulfills the following two
conditions should be selected: (1) The hypothesis is not falsified by
the test(s) used, and (2) it offers the largest domain of
explanation
has the highest explanatory power. That is, the
hypothesis' basic function is to offer the best understanding of
facts. Facts, but not all of them, decide about the rightfulness of
hypotheses. A "good" hypothesis is one that clearly proposes a new
interpretation of facts and consequently can be easily falsified.
In contrast to Goodman's view, we conclude that hypotheses are not limitations to science. Quite the contrary: Facts decide which hypotheses survive and which die; ergo, facts are limitations to hypotheses not the other way around. Survival of a hypothesis that does not conform to the facts is simply an "adjustment" to the specific set of facts that are explained by the hypothesis. A hypothesis' natural death is the lack of such an adjustment or, in the extreme case, empty explanatory space. Therefore, contrary to Goodman's assertion, research is not limited by hypotheses but, rather, experimental data (facts) decide if our hypotheses posses the required explanatory power. The more numerous and heterogeneous the sets of facts are, the more interesting the hypotheses, and the better the chance for an interesting discovery.
Editor's Response
The Editorial published in the August issue of Genome
Research (Goodman 1999
) was meant only to focus on the current
perception in laboratories and especially funding agencies that all
scientific studies should begin first with a hypothesis. (It is agreed
that this is not a new idea; however, current policies and teaching have tended to cement hypothesis-first into current practice.) In this
regard, in focusing on another point, the Editorial did not
appropriately indicate how hypotheses should be handled after they are
made and erroneously spoke of "proving" a hypothesis. Thus, the
authors above make an extremely important point; one that is wholly
agreed with here. Unlike mathematical theorems, hypotheses in other
scientific fields, especially molecular biology, cannot be proven but
can only be accepted as true until proven false. In this regard, the
best hypotheses (no matter what stage in the scientific process they
are generated) are those that can be best tested for falseness. One
additional note, the method for scientific procedure proposed in the
Editorial was meant to be clearly indicated in the following order:
[G] experimental data
Pattern's discovery
THEN
Hypotheses
after which hypotheses undergo appropriate
testing. For hypothesis-free data collection, testable hypotheses
should not need to be formed until general patterns are noted from the data.
Laurie Goodman
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FOOTNOTES |
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3 Corresponding author.
E-MAIL makalowski{at}ncbi.nlm.nih.gov; FAX (301) 480-9241.
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REFERENCES |
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astowski, K.
1996.
In
In New trends in molecular biology, genetic engineering, and medicine. (English translation), pp. 9-26. Sorus, Poznañ, Poland.
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