AML28: The variant allele frequencies of somatic single nucleotide...
In SamGG/densitycut: An Efficient and Versatile Topological Approach to Clustering Biological Data
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
x. A matrix of allele frequencies
y. Clustering labels from the original publication
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.
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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
x. A matrix of allele frequencies
y. Clustering labels from the original publication
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).
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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