MEL5: 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 the lung/pancreatic metastasis of a melanoma patient
Usage
1
Format
A list with one field
x. A matrix of allele frequencies
References
Ding, L., Kim, M., Kanchi, K. L., Dees, N. D., Lu, C., Griffith, M., Fenstermacher,
D., Sung, H., Miller, C. A., Goetz, B., et al. (2014). Clonal architectures and driver
mutations in metastatic melanomas. PLoS ONE, 9(11).
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 the lung/pancreatic metastasis of a melanoma patient
Usage
1 |
Format
A list with one field
x. A matrix of allele frequencies
References
Ding, L., Kim, M., Kanchi, K. L., Dees, N. D., Lu, C., Griffith, M., Fenstermacher, D., Sung, H., Miller, C. A., Goetz, B., et al. (2014). Clonal architectures and driver mutations in metastatic melanomas. PLoS ONE, 9(11).
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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