newSVcalling: Takes as an input an aggregate prob table and call each...
In friendsofstrandseq/MaRyam: Genotyping Structural Variants from single-cell Strand-seq data.
Description
Usage
Arguments
Author(s)
Description
Takes as an input an aggregate prob table and call each segment by the haplotype of the highest probability.
Usage
1
newSVcalling(aggProbTable, haplotypeMode = FALSE)
Arguments
aggProbTable
A matrix containing the logarithm of aggregate probabilities of haplotype states in segments, (rows correspond to segments and columns correspond to haplotype state).
haplotypeMode
TODO ...
Author(s)
Maryam Ghareghani
friendsofstrandseq/MaRyam documentation built on May 28, 2019, 8:40 p.m.
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Description Usage Arguments Author(s)
Description
Takes as an input an aggregate prob table and call each segment by the haplotype of the highest probability.
Usage
1 | newSVcalling(aggProbTable, haplotypeMode = FALSE)
|
Arguments
aggProbTable |
A |
haplotypeMode |
TODO ... |
Author(s)
Maryam Ghareghani
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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