Low-cost air pollution monitors are increasingly being deployed to enrich knowledge about ambient air-pollution at high spatial and temporal resolutions. However, unlike regulatory-grade (FEM or FRM) instruments, universal quality standards for low-cost sensors are yet to be established and their data quality varies widely. This mandates thorough evaluation and calibration before any responsible use of such data. This study presents evaluation and field-calibration of the PM data from a network of low-cost monitors currently operating in Baltimore, MD, which has only one regulatory PM monitoring site within city limits. Co-location analysis at this regulatory site in Oldtown, Baltimore revealed high variability and significant overestimation of PM levels by the raw data from these monitors. Universal laboratory corrections reduced the bias in the data, but only partially mitigated the high variability. Eight months of field co-location data at Oldtown were used to develop a gain-offset calibration model, recast as a multiple linear regression. The statistical model offered substantial improvement in prediction quality over the raw or lab-corrected data. The results were robust to the choice of the low-cost monitor used for field-calibration, as well as to different seasonal choices of training period. The raw, lab-corrected and statistically-calibrated data were evaluated for a period of two months following the training period. The statistical model had the highest agreement with the reference data, producing a 24-hour average root-mean-square-error (RMSE) of around 2 . To assess transferability of the calibration equations to other monitors in the network, a cross-site evaluation was conducted at a second co-location site in suburban Essex, MD. The statistically calibrated data once again produced the lowest RMSE. The calibrated PM readings from the monitors in the low-cost network provided insights into the intra-urban spatiotemporal variations of PM in Baltimore.
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http://dx.doi.org/10.1016/j.atmosenv.2020.117761 | DOI Listing |
JCI Insight
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Department of Biomedical Engineering, Oregon Health and Science University, Portland, United States of America.
Spatial profiling of tissues promises to elucidate tumor-microenvironment interactions and generate prognostic and predictive biomarkers. We analyzed single-cell, spatial data from three multiplex imaging technologies: cyclic immunofluorescence (CycIF) data we generated from 102 breast cancer patients with clinical follow-up, and publicly available imaging mass cytometry and multiplex ion-beam imaging datasets. Similar single-cell phenotyping results across imaging platforms enabled combined analysis of epithelial phenotypes to delineate prognostic subtypes among estrogen-receptor positive (ER+) patients.
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Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Ischemic stroke is a major cause of adult disability. Early treatment with thrombolytics and/or thrombectomy can significantly improve outcomes; however, following these acute interventions, treatment is limited to rehabilitation therapies. Thus, the identification of therapeutic strategies that can help restore brain function in the post-acute phase remains a major challenge.
View Article and Find Full Text PDFJ Clin Invest
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Department of Biochemistry, Molecular Biology & Biophysics, University of Minnesota, Minneapolis, United States of America.
Eccentric contraction- (ECC) induced force loss is a hallmark of murine dystrophin-deficient (mdx) skeletal muscle that is used to assess efficacy of potential therapies for Duchenne muscular dystrophy. While virtually all key proteins involved in muscle contraction have been implicated in ECC force loss, a unifying mechanism that orchestrates force loss across such diverse molecular targets has not been identified. We showed that correcting defective hydrogen sulfide (H2S) signaling in mdx muscle prevented ECC force loss.
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