AML28: The variant allele frequencies of somatic single nucleotide...

Description Usage Format References

Description

The variant allele frequencies of somatic single nucleotide variants from whole genome sequencing of a AML patient at two time points

Usage

1

Format

A list with two fields

References

Miller, C. A., White, B. S., Dees, N. D., Griffith, M., Welch, J. S., Griffith, O. L., Vij, R., Tomasson, M. H., Graubert, T. A., Walter, M. J., et al. (2014). SciClone: Inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolution. PLoS Comput. Biol., 10(8).


SamGG/densitycut documentation built on Oct. 30, 2019, 11:48 p.m.