Study Description


The accurate identification of structural variations using whole-genome DNA sequencing data... Show More

Study Accession Alternative Stable ID type
phs000340.v2.p1 dbGaP Whole Genome Sequencing; Tumor vs. Matched-Normal; Case Set

Who controls access to this study

Extramural NCI Data Access Committee
Access information:



Data provider(s)

  • Title Name Institute
    Principal Investigator Charles Mullighan, MD Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, USA

Who archives the data?

The database of Genotypes and Phenotypes (dbGaP)