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Airborne PM 2.5 samples were collected on fiberglass filters (E558 X 10IN, 254 mm × 203 mm) using a high-volume collector (AVG MP 2.5, 1.13 m/mim) for 24 h for site 1 and site 2 and 6 h for site 3. Four monthly samplings were performed for each site of study.
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An audit of each site evaluating the study protocol, data collection, patient confidentiality and consenting process was completed ∼6 9 months after the site-initiated patient enrollment.
The responder of each site informed the study coordinator once a patient who met the criteria for inclusion signed the informed assent.
Each site had a study team of six people assigned to it.
This is a critical test to assure proper digestion of each site to be studied.
Related site Abstract of study.
Related site Summary of study.
Ethical approval was obtained at each of the enrolling sites of this study.
The study protocol and amendments were reviewed and approved by the institutional review board/independent ethics committee for each site before initiation of the study (see Table S1 for enrollment by site).
Institutional review board approval was obtained at each site before initiation of the study, and all the subjects gave written informed consent.
Thus, for each modified site under study, the dimension of feature vector representing its sequence context was 21 ∗21.
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