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The Human Investigation Committee of Yale University approved our study protocol, and written informed consent for research purpose was obtained from all participants before the procedure.
Informed consent to use the collected data for research purpose was obtained from all participant's parents.
Written informed consent for the use of brain tissue and clinical data for research purpose was obtained from all patients or their next of kin.
Informed consent for blood sampling as a part of daily practice and later use of the data for academic purpose was obtained from all patients or their family members when the patients were admitted to the ICU.
The dataset for this purpose was obtained by integrating manually curated targets from TDR, high confidence targets from UniProt, and attractive targets obtained by Raman et al. [ 29] through a series of comprehensive filters.
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All the reagents and kits used for this purpose were obtained from Exiqon (Exiqon, Vedbaek, Denmark).
As a routine procedure, a signed informed consent to release diagnostic records for scientific purposes was obtained from the parents of the subjects prior to entry into the treatment.
Informed parental consent for post-mortem examination and tissue collection for research purposes was obtained in all cases.
Consent for removal of the tissue and its storage in the tumor bank for research purposes was obtained and documented in the patient's medical chart.
Oral consent for removal of the tissue and its storage in the tumor bank for research purposes was obtained and documented in the patient's medical chart.
Permission for using the information in the medical records of the patients for research purposes was obtained from the 309 Hospital.
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CEO of Professional Science Editing for Scientists @ prosciediting.com