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update
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thierrygosselin committed Sep 2, 2015
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2 changes: 1 addition & 1 deletion R/haplo2colony.R
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# From STACKS haplotypes file wirte COLONY input files to the working directory
# From STACKS haplotypes file write COLONY input files to the working directory

# to get rid of notes in build check
if(getRversion() >= "2.15.1") utils::globalVariables(c("Catalog ID", "Catalog.ID", "Catalog.ID = LOCUS", "Catalog.ID = `Catalog ID`", "Cnt", "HAPLOTYPES", "SAMPLES", "ALLELE", "ALLELE1", "ALLELE2", "GENOTYPE", "NUCLEOTIDES", "INDIVIDUALS", "POP_ID", "POLYMORPHISM", "POLYMORPHISM_MAX", "other", "strata", "hierarchy", "GROUP", "N", "."))
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3 changes: 2 additions & 1 deletion README.md
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Expand Up @@ -56,7 +56,8 @@ This however requires manual curation of the file to work directly with COLONY.

## Roadmap of future developments:

* Very soon: Joint Allele Frequency Spectrum from a *batch_x.sumstats.tsv* or a *batch_x.haplotypes.tsv* files
* Very soon: Map-independent imputation of a VCF using Random Forest or the
most frequent category and Joint Allele Frequency Spectrum from a *batch_x.sumstats.tsv* or a *batch_x.haplotypes.tsv* files
* Re-Integration with [strataG] (https://github.com/EricArcher/strataG.devel/tree/master/strataG.devel)
* Improved documentation and vignette
* Workflow tutorial
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