{"database":"EVA","file_versions":[],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":0,"searchCount":0},"additional":{"dataset_type":["Whole Genome Sequencing"],"omics_type":["Genomics"],"submitter":["EMBL-EBI"],"instrument_platform":["-"],"species":["Homo Sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/eva/?eva-study=PRJEB30460"],"repository":["EVA"],"name_synonyms":["Genomes."],"description_synonyms":["Adoptions., 548, Genomes"],"citation_count":["0"],"additional_accession":[]},"is_claimable":false,"name":"Variant calling on GRCh38 with the 1000 genomes samples","description":"We present biallelic SNVs called from 2,548 samples across 26 populations from the 1000 Genomes Project, called directly against GRCh38. We believe this will be a useful reference resource for those working on GRCh38, representing an improvement over the “lift-overs” of 1000 Genomes data that have been available to date and providing a resource necessary for the full adoption of GRCh38 by the community.","dates":{"publication":"2018-12-19"},"accession":"PRJEB30460","cross_references":{"TAXONOMY":["9606"]}}