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. Name : General Research Use Consent Group # : 1 Abbreviation : GRU
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 University of North Carolina - Chapel Hill (MH090936), North Carolina State University (MH101819),Harvard University (MH090948), Stanford University (MH101782), Washington University (MH101810), and to the University of Pennsylvania (MH101822). The datasets used for the analyses described in this manuscript were obtained from dbGaP at xxxx://xxx.xxxx.xxx.xxx.xxx/gap through dbGaP accession number xxx000XXX.xX.xX – please insert relevant accession numbers. Name : General Research Use Consent Group # : 1 Abbreviation : GRU
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Acknowledgement Statement. This work was supported by grant OT2 HL157968-01 to X. Xxxxxxxxxx from the National Heart, Lung, and Blood Institute (NHLBI), a part of the National Institutes of Health (NIH). For publications, written, and/or oral presentations resulting from use of this data, please cite the following information: “We would like to thank the ACTIV-4A Antithrombotic Strategies Investigators. The original data description for ACTIV-4 ACUTE A Multicenter, Adaptive, Randomized Controlled Platform Trial of the Safety and Efficacy of Antithrombotic Strategies in Hospitalized Adults with COVID-19 (ACTIV4A) can be found here: (Journal Citation )(PMID ). The original data used for the analysis in this publication can be found in the NIH database of Genotypes and Phenotypes (dbGaP) under the accession number phs .” Name : General Research Use Consent Group # : 1 Abbreviation : GRU
Acknowledgement Statement. This work was supported by P01 CA 55819 from the National Cancer Institute. LR was funded by the Deutsche Krebshilfe via the MSNZ program Würzburg, and the Interdisciplinary Center for Clinical Research Würzburg (IZKF). NW was supported by the National Institute of General Medical Sciences of the National Institutes of Health under Award Number P20GM125503, FM was supported by the American Society of Hematology and by Xxxxxxxxx Comprehensive Cancer Center NCI Core Grant (P30 CA 240139). GJM was supported by the Leukemia and Lymphoma Society. Name : General Research Use Consent Group # : 1 Abbreviation : GRU
Acknowledgement Statement. This study was funded by the intramural research program of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health. This work was supported by the National Cancer Institute (CA55727, X.X. Xxxxxxxxx, Principal Investigator). Support to St. Jude Children’s Research Hospital also provided by the Cancer Center Support (CORE) grant (CA21765, X. Xxxxxxx, Principal Investigator) and the American Lebanese-Syrian Associated Charities (ALSAC). This work was supported by grants to L.G.S. from the National Institutes of Health U01CA122371, and from The Xxxx Xxxxxxx Osteosarcoma Fund of Children's Cancer Research Fund. University of Minnesota sequencing was funded by a 2013 Hyundai Hope of Wheels Grant in addition to the other sources. Research is supported by the Chair's Grant U10 CA98543 and Human Specimen Banking Grant U24 CA114766 of the Children's Oncology Group from the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Additional support for research is provided by a grant from the WWWW (QuadW) Foundation, Inc. to the Children's Oncology Group. The work of A.P.G was supported by the Departamento De Salud, Gobierno Xx Xxxxxxx, Proyectos de Biomedicina 2018. A.P.G. was also funded by La Fundación "La Caixa”- Caja Navarra, PI13/01476, FIS, ISCIII. F.L. was funded by and AECC, FIMA (Foundation for Applied Medical Research), Cancer Research Thematic Network of the Instituto de Xxxxx Xxxxxx XXX (RTICC RD 12/0036/0066), CIBERONC (CB16/12/00443 and CB16/12/00350) and the Spanish Ministry of Economy and Competitiveness (RTI2018-094507-B-100). This study was also supported by biobank grants from the Regione Emilia-Romagna, by the infrastructure and personnel of the Royal National Orthopaedic Hospital Musculoskeletal Research Programme and Biobank. Support was also provided to A.M.F. (UCL) by the National Institute for Health Research UCLH Biomedical Research Centre, and UCL Experimental Cancer Centre. The work of A.M.F. was supported by the Bone Cancer Research Trust UK. The International Sarcoma Kindred Study was supported by the Rainbows for Xxxx Foundation, the Xxxxx Xxxxxxx Sarcoma Initiative, the Victorian Cancer Agency, the Australian National Health and Medical Research Council (APP1004017) and Cancer Australia (APP1067094). Name : Health/Medical/Biomedical Consent Group # : 1 Abbreviation : HMB or ancestry.
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. Name : Disease-Specific (Platelet Function, RD) Consent Group # : 1 Abbreviation : DS-PF-RD
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