Comments (5)
R/qtl is intended for QTL analysis of data from simple crosses between inbred lines, such as a backcross or intercross. The input format is rather specific; see Chapter 2 of the R/qtl book.
The Data.csv file within the Data.zip file that you provide is tab-delimited, so you would need to use sep="\t"
in the call to read.cross()
, but the main problems are that you shouldn't include the founder strains, you would need many more than two individuals, and you would need to restructure the data file a bit; see the sample CSV data files at http://www.rqtl.org/sampledata/.
from qtl.
from qtl.
I don't completely understand what you mean, but you could could use the "csvr" format where the rows are phenotypes and then markers, and the columns are individuals. Here's an example from the R/qtl book, chapter 2 pg 29:
from qtl.
from qtl.
There's a c.cross()
function that can be used to combine two crosses. Or you could load the two datasets, analyze them separately, and compare the results.
from qtl.
Related Issues (20)
- scanone perms with 4-way cross giving all 0's HOT 3
- Change read.cross warning about length of arg alleles
- pull.rf gives error with duplicate marker names
- GH Action check failing on MacOS HOT 2
- stepwiseqtl has problems with X chr and sex covariate HOT 1
- Problem in scantwo permutations HOT 1
- addcovar arg for cim()
- addtoqtl should clear attributes HOT 1
- Error: "long vectors (argument 5) are not supported in .C" HOT 2
- switch.alleles should give error with results of markerlrt HOT 1
- reduce2grid error HOT 2
- locationXO and countXO for BCsFt
- addint bug when X chr QTL and missing phenotypes HOT 2
- summary.scanone error with threshold as a vector
- Improper header in pheno dataframe with single column pheno file HOT 3
- Warning on CRAN
- Additional warnings on CRAN
- Error handling of pheno.col in cim()
- Compilation error on R-devel HOT 3
- Calloc/Realloc can no longer be used? HOT 1
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