import_snvs: SNV Importer This function imports SNVs from a tab-delimited...
In eyzhao/hrdtools: Homologous Recombination Deficiency Tests with Whole Genome Sequencing
Description
SNV Importer
This function imports SNVs from a tab-delimited file. The file must be formatted
in at least 4 tab-separated columns. The first four columns of the file must be
chromosome number (without 'chr'), position, reference base, mutant base.
Usage
1
import_snvs(path, genomeVersion = "hg19", hasHeader = FALSE)
Arguments
path
Path to the tab-delimited SNV data file
eyzhao/hrdtools documentation built on May 21, 2019, 3:09 a.m.
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Description
SNV Importer This function imports SNVs from a tab-delimited file. The file must be formatted in at least 4 tab-separated columns. The first four columns of the file must be chromosome number (without 'chr'), position, reference base, mutant base.
Usage
1 | import_snvs(path, genomeVersion = "hg19", hasHeader = FALSE)
|
Arguments
path |
Path to the tab-delimited SNV data file |
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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