{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Rockowitz S"],"funding":["NICHD NIH HHS","NIDDK NIH HHS"],"pagination":["29"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC7338382"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["5"],"pubmed_abstract":["While genomic data is frequently collected under distinct research protocols and disparate clinical and research regimes, there is a benefit in streamlining sequencing strategies to create harmonized databases, particularly in the area of pediatric rare disease. Research hospitals seeking to implement unified genomics workflows for research and clinical practice face numerous challenges, as they need to address the unique requirements and goals of the distinct environments and many stakeholders, including clinicians, researchers and sequencing providers. Here, we present outcomes of the first phase of the Children's Rare Disease Cohorts initiative (CRDC) that was completed at Boston Children's Hospital (BCH). We have developed a broadly sharable database of 2441 exomes from 15 pediatric ra"],"journal":["NPJ genomic medicine"],"pubmed_title":["Children's rare disease cohorts: an integrative research and clinical genomics initiative."],"pmcid":["PMC7338382"],"funding_grant_id":["P30 DK034854","U54 HD090255"],"pubmed_authors":["Quitadamo A","Sexton E","Kornetsky S","Rockowitz S","Field M","Park M","Smith L","Brownstein CA","Wang L","Agrawal PB","Beggs AH","Williams DA","Poduri A","LeCompte N","Snapper SB","Carmack M","Yu TW","Holm IA","Knight D","Sheidley B","Sliz P"],"additional_accession":[]},"is_claimable":false,"name":"Children's rare disease cohorts: an integrative research and clinical genomics initiative.","description":"While genomic data is frequently collected under distinct research protocols and disparate clinical and research regimes, there is a benefit in streamlining sequencing strategies to create harmonized databases, particularly in the area of pediatric rare disease. Research hospitals seeking to implement unified genomics workflows for research and clinical practice face numerous challenges, as they need to address the unique requirements and goals of the distinct environments and many stakeholders, including clinicians, researchers and sequencing providers. Here, we present outcomes of the first phase of the Children's Rare Disease Cohorts initiative (CRDC) that was completed at Boston Children's Hospital (BCH). We have developed a broadly sharable database of 2441 exomes from 15 pediatric ra","dates":{"release":"2020-01-01T00:00:00Z","publication":"2020","modification":"2025-04-19T18:00:55.282Z","creation":"2025-04-19T18:00:55.282Z"},"accession":"S-EPMC7338382","cross_references":{"pubmed":["32655885"],"doi":["10.1038/s41525-020-0137-0"]}}