Acknowledgement Statement. The results published here are in whole or part based upon data generated by The Cancer Genome Atlas managed by the NCI and NHGRI. Information about TCGA can be found at xxxx://xxxxxxxxxxxx.xxx.xxx.
Acknowledgement Statement. The Genotype-Tissue Expression (GTEx) Project was supported by the Common Fund of the Office of the Director of the National Institutes of Health (xxxxxxxxxx.xxx.xxx/XXXx). Additional funds were provided by the NCI, NHGRI, NHLBI, NIDA, NIMH, and NINDS. Donors were enrolled at Biospecimen Source Sites funded by NCI\Leidos Biomedical Research, Inc. subcontracts to the National Disease Research Interchange (10XS170), Roswell Park Cancer Institute (10XS171), and Science Care, Inc. (X10S172). The Laboratory, Data Analysis, and Coordinating Center (LDACC) was funded through a contract (HHSN268201000029C) to the The Broad Institute, Inc. Biorepository operations were funded through a Leidos Biomedical Research, Inc. subcontract to Xxx Xxxxx Research Institute (10ST1035). Additional data repository and project management were provided by Leidos Biomedical Research, Inc.(HHSN261200800001E). The Brain Bank was supported supplements to University of Miami grant DA006227. Statistical Methods development grants were made to the University of Geneva (MH090941 & MH101814), the University of Chicago (MH090951,MH090937, MH101825, & MH101820), the
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Acknowledgement Statement. All published scientific findings derived from tissues and/or data obtained through the NeuroBioBank must acknowledge the “NIH NeuroBioBank” as the source. NIH NeuroBioBank must be notified of any publications so that the publication can be linked to the tissues or data. Data Release Principles and Standards. Data from NeuroBioBank tissues are expected to be shared in an easily accessible format so as to increase the value of the significant public investment.
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Acknowledgement Statement. This study is funded by the Intramural program at the NHGRI/NIH. The study dataset was created using two human samples and 20 daughter lines which were established clonally to compare mutation frequencies among samples. One human sample is obtained from a patient with blood disorder (Xxxxxxxx XX, Blood, 2014) and one human sample is obtained from a collaborator, Xx. Xxxxx Xxxxxx, at the NHLBI (CTRL-1 from Xxxxxx T, JCI, 2013). Whole exome sequencing and targeted deep sequencing was performed in addition to SNP arrays to detect variations among the samples.
Acknowledgement Statement. This research was supported by the Intramural Research Program of the NIMH(NCT00001260, 900142).
Acknowledgement Statement. Xxxxxxxxxxxxx E, Xxxxxx XX, Xxxxxxxx R, Xxxx J, Xxxx MR, Xxxxxxxxx S, Xxxxx D, Xxxxxx XX, and Xxxxxxxxxxxx X. "Evaluation of hybridization capture versus amplicon-based methods for whole exome sequencing." In press for Human Mutation. E.S. is supported by a Pelotonia Postdoctoral fellowship. S.D. is supported by an American Society of Clinical Oncology Young Investigator Award. S.R. is supported by the American Cancer Society (MRSG-12-194-01-TBG), a Prostate Cancer Foundation Young Investigator Award, NHGRI (UM1HG006508-01A1), Fore Cancer Research Foundation, and Pelotonia.
Acknowledgement Statement. Centre for Cognitive Ageing and Cognitive Epidemiology (Pilot Fund award), Age UK, The Wellcome Trust Institutional Strategic Support Fund, The University of Edinburgh, and The University of Queensland. The Lothian Birth Cohorts work was done in the University of Edinburgh Centre for Cognitive Ageing and Cognitive Epidemiology which is supported by funding from the BBSRC, the UK’s Medical Research Council, and the University of Edinburgh as part of the cross-council Lifelong Health and Wellbeing initiative (MR/K026992/1).
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