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DNA sequence data for the processed ChIP regions for each cell line were retrieved from the UCSC database [58].
Details of the CD markers used for cell isolation together with quality control data for the processed samples are given in Tables S1 and S2.
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Published real industrial scale data for the process was used as a basis for validating the process model.
This technology could provide meaningful original data for the process design and optimization of typical and novel crystallization processes.
Inventory data for the processes involved in the study were taken from the EcoInvent database 2010 [14], the JEMAI, and from literature that examined the existing local processes.
As a next step that data set has been processed once by the BERNESE software resulting in new physical orbits which are then our starting data for the process flow described in the 'Processing' subsection (see also Fig. 2).
Data for the process evaluation were collected from the patients by means of self-administered questionnaires.
The data for the process evaluation will be collected with by means of specifically developed evaluation questionnaires.
Time registration and patient drop-out data for the process analysis will be collected using registrations made by the RA and the NPs.
Data for the process evaluation will be gathered continuously over the study period and focus on recruitment, reach, dose delivered and dose received.
Data for the process evaluation will be obtained via the course evaluation questionnaire at T1. Data from the non-response questionnaire will be used to assess reasons for not completing the Internet course.
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