Cite
HARVARD Citation
Ainscough, B. et al. (2018). A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data. Nature genetics. pp. 1735-1743. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Ainscough, B. et al. (2018). A deep learning approach to automate refinement of somatic variant calling from cancer sequencing data. Nature genetics. pp. 1735-1743. [Online].