Cite
HARVARD Citation
Kader, T. et al. (2016). Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue. Genome medicine. 8 (1), pp. 1-13. [Online].
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Kader, T. et al. (2016). Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue. Genome medicine. 8 (1), pp. 1-13. [Online].