Additional file 3 of ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

Minoche, Andre E.; Lundie, Ben; Peters, Greg B.; Ohnesorg, Thomas; Pinese, Mark; Thomas, David M.; Zankl, Andreas; Roscioli, Tony; Schonrock, Nicole; Kummerfeld, Sarah; Burnett, Leslie; Dinger, Marcel E.; Cowley, Mark J.

doi:10.6084/m9.figshare.14121554.v1

13073_2021_841_MOESM3_ESM.pdf (198.15 kB)

Additional file 3 of ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

journal contribution

posted on 2021-02-26, 04:29 authored by Andre E. Minoche, Ben Lundie, Greg B. Peters, Thomas Ohnesorg, Mark Pinese, David M. Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld, Leslie Burnett, Marcel E. Dinger, Mark J. Cowley

Additional file 3. Sample automated QC report NA12878. ClinSV’s automated QC report for control sample NA12878.

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Kinghorn Foundation Cancer Institute NSW NSW Health

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Structural variation Copy number variation Whole genome sequencing Microarray Clinical genome Rare disease

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Additional file 3 of ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data

Funding

Kinghorn Foundation Cancer Institute NSW NSW Health

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