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Although the in vivo and in vitro datasets were generated from different experimental materials as well as different instruments, they both stem from the same cell type: monocyte.
Both worm and fly datasets were generated from Two-hybrid assays.
Affymetrix microarray datasets were generated from the liver and kidney of all individual control and treated animals.
To test these hypotheses, datasets were generated from pelagic water samples taken from the L4 station during the day and night at 3 sampling time points in 2008: January, April and August, representing winter, spring and summer.
Finally, datasets were generated from the model.
The datasets were generated from version 44.3 and 44.4 of SWISS-PROT [ 18].
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Simulated iris datasets are generated from two scenarios.
Those datasets are generated from a variety of sources having different representation forms and formats.
For time complexity comparison, different sizes of datasets are generated from this dataset by cutting this promoter region dataset.
The low-coverage datasets are generated from independent samples using different sequencing platforms and different versions of library-prep kits.
In addition, de-identified datasets are generated from the central database for the research community to query (the so-called safe harbor approach to HIPAA-compliance) [ 7].
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