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Attached is household survey data (refer to variables B6.2.1a B6236c2) and FGD tool used in the study (applicable questions to this manuscript are in part C of the tool)—provided as Additional files 1, 2, 3. It's instructive to note here that data and results in this manuscript were derived from a PhD thesis of the first author (Recha 2013, Kenyatta University, unpublished).
Subsequently, all data presented in the manuscript were derived from Subset 1 classified at 95% confidence level.
The patients in the manuscript were derived from two different Phase I studies and a Phase II study using different IGF1R inhibitors and all the studies have been registered in www.clinicaltrials.gov.gov
All qPCR data in this manuscript were derived using the probes as described in Figure 1.
The sample sizes reported in this manuscript were derived from normalized weights, weighted to represent a larger population.
The global transcriptome data evaluated within this manuscript were derived from an earlier study on rectal suction biopsies, which include 16 unrelated homozygotes for c.1521_1523delCTT in CFTR, who were enrolled for their ICM phenotype as described above.
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This manuscript is derived from the thesis of the Corresponding Author, SH.
The data presented in the manuscript are derived from SRM channels detecting the fatty acid fragment with more unsaturation (or the longer one when both have the same unsaturation), but only molecules that were detected in SRM channels for both fatty acid fragment with consistent retention times were analyzed.
Column five presents the PubMed ID associated with the manuscript from which the sequences were derived.
In the main body of the manuscript, sensitivity, specificity and accuracy were derived from training result of the classification.
The remaining ~1 k transcripts were the subject of analysis in the current manuscript, under the assumption that they were derived from extraneous organisms, pathogens or commensal, inhabiting the twenty different tissues.
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