scores: MAPEX scores for the passed variants in 'variants'
In bmannakee/mapexr: Sensitive and Specific Filtering of Genetic Variants in Xenograft and Primary Tumors
Description
MAPEX scores for the passed variants in variants
Usage
1
Format
MAPEX scores
- chrom
The chromosome the variant is on
- loc
The genomic coordinates of the SNV
- variant_score
The variant score (between 0.0 and 1.0)
- reason
The most common classification of reads supporting the variant (mouse,on_target,off_target)
bmannakee/mapexr documentation built on May 5, 2019, 12:27 p.m.
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Description
MAPEX scores for the passed variants in variants
Usage
1 |
Format
MAPEX scores
- chrom
The chromosome the variant is on
- loc
The genomic coordinates of the SNV
- variant_score
The variant score (between 0.0 and 1.0)
- reason
The most common classification of reads supporting the variant (mouse,on_target,off_target)
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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