Description Usage Arguments Value References Examples
Genetic divergence between regions of subclonal sSNVs using the Weir and Cockerham method
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 |
maf |
A Maf or MafList object generated by |
patient.id |
Select the specific patients. Default NULL, all patients are included. |
min.vaf |
Specify The minimum VAF to filter variants. Default 0. |
min.total.depth |
The minimum total allele depth for filtering variants. Default 2. |
use.adjVAF |
Use adjusted VAF in analysis when adjusted VAF or CCF is available. Default FALSE. |
plot |
Logical (Default: TRUE). |
withinTumor |
Logical (Default: FALSE). Whether calculate between-region heterogeneity within tumors. |
use.circle |
Logical (Default: TRUE). Whether use "circle" in the plot. as visualization method of correlation matrix |
title |
The title of the plot. Default "Nei's distance" |
number.cex |
The size of text shown in correlation plot. Default 8. |
number.col |
The color of text shown in correlation plot. Default "#C77960". |
use.tumorSampleLabel |
Logical (Default: FALSE). Rename the 'Tumor_Sample_Barcode' by 'Tumor_Sample_Label'. |
... |
Other options passed to |
A list contains Fst value of MRS and Hudson estimator of each sample-pair, respectively.
Sun R, Hu Z, Sottoriva A, et al. Between-region genetic divergence reflects the mode and tempo of tumor evolution. Nat Genet. 2017;49(7):1015-1024.
Bhatia G, Patterson N, Sankararaman S, Price AL. Estimating and interpreting FST: the impact of rare variants. Genomic Res. 2013;23(9):1514-1521.
1 2 3 4 5 | maf.File <- system.file("extdata/", "CRC_HZ.maf", package = "MesKit")
clin.File <- system.file("extdata/", "CRC_HZ.clin.txt", package = "MesKit")
ccf.File <- system.file("extdata/", "CRC_HZ.ccf.tsv", package = "MesKit")
maf <- readMaf(mafFile=maf.File, clinicalFile = clin.File, ccfFile=ccf.File, refBuild="hg19")
calFst(maf)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.