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In a recent simulation study using realistic parameter estimates for human data, Messer and Petrov [ 65] demonstrated that linked selection can lead to significant skews in synonymous site frequency spectra, to the extent that demographic expansions were falsely inferred.
Note that our results do not demonstrate LBA in the usual manner, whereby sequence data generated from a Felsenstein-zone four taxa tree where a pair of long and short external branches are separated from one another by a short internal branch are falsely inferred by parsimony to come from a tree where the two long branches group together.
The secondary failure of inference is when the ensuing percept (and any somatosensory consequences) is falsely inferred to be a symptom to explain why its content was not predicted by the source of attentional modulation.
Based on expression data only, the modeling of TF activity can lead to falsely inferred interactions.
SSE are likely to bias estimates of sequence diversity as they will lead to falsely inferred SNPs in specific error prone sites.
Most of the falsely inferred DDIs are due to the extraction of incorrect < drug, induces, protein> and < drug, inhibits, protein> relations.
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Furthermore, we show that for the mapped zonation, the difference between predicted 4He/3He data for a uniform crystal and a 3D model of the crystal are minimal, highlighting that zonation is unlikely to lead us to falsely infer an "old" Grand Canyon.
In this case, we would be falsely inferring the duplications and relocations as lineage specific.
The maximum χ2 test of recombination is one of the most powerful tests of recombination [ 90] but it can occasionally falsely infer the presence of recombination under some conditions, such as in regions that contain mutational hot-spots [ 91].
We note that BiSSE is currently the best method to test character state irreversibility, as it is less prone to falsely infer reversions [ 7, 14], and has been used previously for clades of similarly small size (e.g., [ 37, 78, 90– 90]).
This statistic is a powerful detector of recombination and has been shown by simulation studies to be less sensitive to the effects of mutation rate correlation than other available statistics, which are prone to falsely infer recombination when levels of recurrent mutation are high [ 25].
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com