consistent_haplotypes_across_loci.read_table: Split read table into loci with no spanning reads, create...
In SLeviyang/RegressHaplo: Haplotype Reconstruction Using Penalized Regression
consistent_haplotypes_across_loci.read_table R Documentation
Split read table into loci with no spanning reads, create consistent
haplotypes for each locus, and then combine to create full haplotypes
Description
Split read table into loci with no spanning reads, create consistent
haplotypes for each locus, and then combine to create full haplotypes
Usage
consistent_haplotypes_across_loci.read_table(
df_in,
min_cover = 500,
max_num_haplotypes = 20000
)
SLeviyang/RegressHaplo documentation built on June 1, 2022, 10:48 p.m.
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| consistent_haplotypes_across_loci.read_table | R Documentation |
Split read table into loci with no spanning reads, create consistent haplotypes for each locus, and then combine to create full haplotypes
Description
Split read table into loci with no spanning reads, create consistent haplotypes for each locus, and then combine to create full haplotypes
Usage
consistent_haplotypes_across_loci.read_table( df_in, min_cover = 500, max_num_haplotypes = 20000 )
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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