View source: R/other_useful_functions.R
convertBlockList | R Documentation |
Function to convert haplotype block list from PLINK to RAINBOWR format
convertBlockList(
fileNameBlocksDetPlink,
map,
blockNamesHead = "haploblock_",
imputeOneSNP = FALSE,
insertZeros = FALSE,
n.core = 1,
parallel.method = "mclapply",
count = FALSE
)
fileNameBlocksDetPlink |
File name of the haplotype block list generated by PLINK (See reference). The file names must contain ".blocks.det" in the tail. |
map |
Data frame with the marker names in the first column. The second and third columns contain the chromosome and map position. |
blockNamesHead |
You can specify the header of block names for the returned data.frame. |
imputeOneSNP |
As default, blocks including only one SNP will be discarded from the returned data. If you want to include them when creating haplotype-block list for RAINBOWR, please set 'imputeOneSNP = TRUE'. |
insertZeros |
When naming blocks, whether or not inserting zeros to the name of blocks. For example, if there are 1,000 blocks in total, the function will name the block 1 as "block_1" when 'insertZeros = FALSE' and "block_0001" when 'insertZeros = TRUE'. |
n.core |
Setting n.core > 1 will enable parallel execution on a machine with multiple cores. This argument is not valid when 'parallel.method = "furrr"'. |
parallel.method |
Method for parallel computation. We offer three methods, "mclapply", "furrr", and "foreach". When 'parallel.method = "mclapply"', we utilize When 'parallel.method = "furrr"', we utilize When 'parallel.method = "foreach"', we utilize We recommend that you use the option 'parallel.method = "mclapply"', but for Windows users, this parallelization method is not supported. So, if you are Windows user, we recommend that you use the option 'parallel.method = "foreach"'. |
count |
When count is TRUE, you can know how far RGWAS has ended with percent display. |
A data.frame object of
Block names for SNP-set methods in RAINBOWR
Marker names in each block for SNP-set methods in RAINBOWR
Purcell, S. and Chang, C. (2018). PLINK 1.9, www.cog-genomics.org/plink/1.9/. Chang CC, Chow CC, Tellier LCAM, Vattikuti S, Purcell SM, Lee JJ (2015) Second-generation PLINK: rising to the challenge of larger and richer datasets. GigaScience, 4. Gaunt T, RodrÃguez S, Day I (2007) Cubic exact solutions for the estimation of pairwise haplotype frequencies: implications for linkage disequilibrium analyses and a web tool 'CubeX'. BMC Bioinformatics, 8. Taliun D, Gamper J, Pattaro C (2014) Efficient haplotype block recognition of very long and dense genetic sequences. BMC Bioinformatics, 15.
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