Associated Papers
Clinical detection of deletion structural variants in whole-genome sequences.
Noll AC et al.
Npj Genomic Medicine, 2016
29263817 (PubMed )
Supplement: npjgenmed201626-s7.xlsx › Sheet1
Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Saunders CJ et al.
Science Translational Medicine, 2012
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