polyRAD (version 1.6)

readHMC: Import read depth from UNEAK

Description

This function reads the “HapMap.hmc.txt” and “HapMap.fas.txt” files output by the UNEAK pipeline and uses the data to generate a “RADdata” object.

Usage

readHMC(file, includeLoci = NULL, shortIndNames = TRUE, 
        possiblePloidies = list(2), contamRate = 0.001, 
        fastafile = sub("hmc.txt", "fas.txt", file, fixed = TRUE))

Value

A RADdata object containing read depth, taxa and locus names, and nucleotides at variable sites.

Arguments

file

Name of the file containing read depth (typically “HapMap.hmc.txt”).

includeLoci

An optional character vector of loci to be included in the output.

shortIndNames

Boolean. If TRUE, taxa names will be shortened with respect to those in the file, eliminating all text after and including the first underscore.

possiblePloidies

A list of numeric vectors indicating potential inheritance modes of SNPs in the dataset. See RADdata.

contamRate

A number ranging from zero to one (typically small) indicating the expected rate of sample cross-contamination.

fastafile

Name of the file containing tag sequences (typically “HapMap.fas.txt”).

Author

Lindsay V. Clark

References

Lu, F., Lipka, A. E., Glaubitz, J., Elshire, R., Cherney, J. H., Casler, M. D., Buckler, E. S. and Costich, D. E. (2013) Switchgrass genomic diversity, ploidy, and evolution: novel insights from a network-based SNP discovery protocol. PLoS Genetics 9, e1003215.

https://www.maizegenetics.net/tassel

https://tassel.bitbucket.io/TasselArchived.html

See Also

readTagDigger, VCF2RADdata, readStacks, readTASSELGBSv2, readDArTag

Examples

# for this example we'll create dummy files rather than using real ones
hmc <- tempfile()
write.table(data.frame(rs = c("TP1", "TP2", "TP3"),
                       ind1_merged_X3 = c("15|0", "4|6", "13|0"),
                       ind2_merged_X3 = c("0|0", "0|1", "0|5"),
                       HetCount_allele1 = c(0, 1, 0),
                       HetCount_allele2 = c(0, 1, 0),
                       Count_allele1 = c(15, 4, 13),
                       Count_allele2 = c(0, 7, 5),
                       Frequency = c(0, 0.75, 0.5)), row.names = FALSE,
            quote = FALSE, col.names = TRUE, sep = "\t", file = hmc)
fas <- tempfile()
writeLines(c(">TP1_query_64",
             "TGCAGAAAAAAAACGCTCGATGCCCCCTAATCCGTTTTCCCCATTCCGCTCGCCCCATCGGAGT",
             ">TP1_hit_64",
             "TGCAGAAAAAAAACGCTCGATGCCCCCTAATCCGTTTTCCCCATTCCGCTCGCCCCATTGGAGT",
             ">TP2_query_64",
             "TGCAGAAAAACAACACCCTAGGTAACAACCATATCTTATATTGCCGAATAAAAAACAACACCCC",
             ">TP2_hit_64",
             "TGCAGAAAAACAACACCCTAGGTAACAACCATATCTTATATTGCCGAATAAAAAATAACACCCC",
             ">TP3_query_64",
             "TGCAGAAAACATGGAGAGGGAGATGGCACGGCAGCACCACCGCTGGTCCGCTGCCCGTTTGCGG",
             ">TP3_hit_64",
             "TGCAGAAAACATGGAGATGGAGATGGCACGGCAGCACCACCGCTGGTCCGCTGCCCGTTTGCGG"),
             fas)

# now read the data
mydata <- readHMC(hmc, fastafile = fas)

# inspect the results
mydata
mydata$alleleDepth
mydata$alleleNucleotides
row.names(mydata$locTable)