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YW provided assistance in microarray study design and data analysis.
IH participated in the microarray study design and drafting of the manuscript.
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LDB normalized the microarray data and provided input into the microarray study designs.
Despite the low coverage of this study (∼0.8× raw sequence coverage and between 2.39× and 5.05× indel coverage per lane), we still detected a lot of variation; our results compare well with previous microarray studies designed to detect copy-number variants.
SKK contributed to the microarray experiment study design, performed the RNA extraction and microarray procedures, and wrote the manuscript.
DWT passed away during the preparation of the manuscript; before his untimely death, he significantly contributed to the microarray and study design and coordination, and provided the microarray facilities.
TS participated in the microarray construction, study design and manuscript writing and cultured the flies and extracted the RNA for the microarray study.
A second microarray study (experimental design B) was used to identify significantly differentially expressed genes by hybridising amplified RNA from aerobic and microaerophilic (NRP1) culture conditions directly against one another.
A GeneChip microarray study was designed to compare gene expression profiles of BZA to that of other SERMs, raloxifene (RAL) and lasofoxifene (LAS).
To enhance our knowledge on the impact of IL-17 alone and combined with TNF-alpha in primary murine hepatocytes a comprehensive microarray study was designed.
DM contributed to the design of the miRNA microarrays and study design.
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