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Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases
Study EGAS00001007575 -
GenomeWideData_for_Present_Day_Peruvian_individuals_living_in_urban_areas
Dataset EGAD00010002795 -
SAFIR02_Agilent
Dataset EGAD00010002243 -
B99
Dataset EGAD00010001427 -
IHIT
Dataset EGAD00010001428 -
EGAD00010000536
Dataset EGAD00010000536 -
WES for Verhaak GBM
Dataset EGAD00001001109 -
WES for verhaak-GBM
Dataset EGAD00001001110 -
Variant_files_100_ID_trios
Dataset EGAD00001000277 -
Complete Genomics dataset for study EGAS00001002275.
Dataset EGAD00001003187
