<HashMap><database>EVA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/H9.vcf.gz.csi</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/H9.vcf.gz</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/PA-1.vcf.gz.csi</Vcf><Vcf>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/PA-1.vcf.gz</Vcf><Other>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/H9.vcf.csi</Other><Other>ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB109977/PA-1.vcf.csi</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><dataset_type>Whole Genome Sequencing</dataset_type><omics_type>Genomics</omics_type><submitter>The University of Queensland</submitter><instrument_platform>Oxford Nanopore PromethION</instrument_platform><species>Homo Sapiens</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJEB109977</full_dataset_link><repository>EVA</repository></additional><is_claimable>false</is_claimable><name>Long-read genomic analysis of human cell lines</name><description>Oxford nanopore technologies (ONT) long-read sequencing was applied to PA-1 cells and H9 hESCs to call heterozygous SNPs and use that information to discriminate active and inactive X chromosome haplotypes.</description><dates><publication>2026-03-15</publication></dates><accession>PRJEB109977</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>