Concepedia

Publication | Open Access

Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease

DOIFull Paper Access

126

Citations

36

References

2018

Year

Andrew M. Gross, Subramanian S. Ajay, Vani Rajan, Carolyn M. Brown, Krista Bluske, Nicole Burns, Aditi Chawla, Alison J. Coffey, Alka Malhotra, Alicia Scocchia,
Genetics in Medicine

Abstract

Robust identification of CNVs by GS is possible within a clinical testing environment.

References

YearCitations

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