After sorting the molecules within a group, the groups representing starting materials and products are sorted using the unix 'sort' command.
Thy1.1-positive cells were sorted using CD90.1 microbeads (Miltenyi Biotec, Bergisch Gladbach, Germany).
Next, the supplied job j is added to the jobsToRemap list (line 2) and then the jobsToRemap list is sorted using RM-DCWF's jobComparator (line 3).
Simple spikes were sorted using hardware window discriminators and digitized.
The results are sorted using LingPipe to improve overall classification and to avoid identical coding and spelling.
The mapping results were sorted using samtools [ 76] and then analyzed with MarkDuplicates module of Picard [ 32].
All individual medication names were sorted using existing medication sub-classes classification from the ODB database, after which medication sub-classes were grouped into specific medication classes.
Single units were sorted using custom software (xclust, M. Wilson at MIT, available at GitHub repository: https://github.com/wilsonlab/mwsoft64/tree/master/src/xclust) on all data recorded across all recoding days.
To obtain a more pure population of neurons for qRT-PCR, mature cultures were sorted using a CD24 MicroBead Kit (130-095-951, Miltenyi Biotec).
Transcripts were sorted using fairly stringent conditions during the first 7 days of storage: up-regulated 5-fold for 1-MCP treatment; up-regulated 2-fold in the control; and either repressed or not changed for DPA treatment.
