M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity
Nature Genetics2016Vol. 48(12), pp. 1581–1586
Citations Over TimeTop 1% of 2016 papers
Karthik A. Jagadeesh, Aaron M. Wenger, Mark J. Berger, Harendra Guturu, Peter D. Stenson, D.N. Cooper, Jonathan A. Bernstein, Gill Bejerano
Related Papers
- → The GENCODE exome: sequencing the complete human exome(2011)63 cited
- → Clinical Exome Performance for Reporting Secondary Genetic Findings(2014)35 cited
- [The application of exome sequencing in human disease].(2014)
- → Exome sequencing for neurological disorders(2017)
- → Abstract 1349: Improved human exome sequencing workflow with the most complete coverage(2020)