Uploading/downloading large data results to/from Galaxy via its graphical user interface can be slow (roughly 20× slower than a direct FTP transfer); furthermore, when a Galaxy cluster is terminated, all its data and results are deleted.
For example, finding a random subset of PubChem compounds in the 94M dataset runs optimally with parameter MinCover = 3, which is closely followed by MinCover = 2 (roughly 4% slower) and MinCover = 4 and 5 (9% and 15% slower).
Cellulose hydrolysis in anaerobic conditions was roughly 30% slower than in the presence of air.
Compared with haploid, maternally transmitted mtDNA, allozymes are diploid and evolve roughly 10× slower with ~4-fold larger Ne and coalescence times (independent of mutation rate), and higher gene-flow rates [ 29, 101, 102].
aIdentifying such a single separation and grouping the state variables roughly into slow and fast families often is a difficult part of the model analysis.
As indicated in Table 1 m SO and h SI are slow variables that vary on a time scale that is (roughly) 10 times slower than m SI and m FO and 100 times slower than V.
The displacement rate is roughly 40 times slower than strand displacement.
Comparing the data with simulations, we estimated that the displacement rate across corners is roughly 100 times slower than that within the same tile edge.
Making matters worse, poor domestic telephone lines mean that the fastest connections here are still roughly 50 times slower than the best lines available to Internet users in the United States.
Comparing the simulations with experimental data, we estimated that the displacement rate for coded branch migration domains is roughly 25 times slower than that for branch migration domains with continuous edge staples.
