To obtain insight into functions of nrFLcDNAs that were not found in other plants, we extracted 694 nrFLcDNAs that matched none of the other plant genes (see Additional file 2: Clone number list).
In other words, we extracted training samples at each pixel location of the training images.
Unlike other constructions, we extracted the mask, maintaining enough memory without the need for complicated optimization criteria.
On the other hand, we extracted proteins with small molecular weight in different mouse sera and subjected to Q Exactive MS detection.
For this reason, we implemented a large number of attribute-based, point-based and other methods; we extracted observable attributes from occluded blobs, in particular, the duration of the occlusion and its minimum number of pixels (providing information about a 'maximal degree of occlusion') turned out to provide good occlusion characterizations.
To determine which interactions have been identified in other organisms, we extracted PPI data for the 72 SSU processome proteins from BioGRID and IntAct for C. elegans, D. melanogaster, H. sapiens, S. pombe, P. falciparum and M. musculus.
To more clearly define the relationships between these proteins and other kinesins, we extracted a set of representative Kinesin-13 sequences from a wide variety of eukaryotes from our previous analysis [17].
For all other interventions we extracted the outcome at the end of treatment.
The transcript counts and other data we extracted will be available on the DRYAD data repository.
To detect H. capsulatum and other fungi, we extracted genomic DNA directly from bat guano by using the silica-guanidine thiocyanate protocol, NucliSense Isolation Reagent (bioMérieux, Boxtel, the Netherlands), according to the manufacturer's protocol.
