Genetics
Click on a subcategory to reveal individual genetics processes.
Subcategory |
Contains processes for... |
Input data requirement1 |
Checking and manipulation of data to improve suitability for subsequent analyses. |
A wide or annotation data set, or both, depending on the process. Note: SNP Power does not require an input data set. |
|
Computation of kinship, relationship, identity, and population statistics. |
Wide, tall, or square data, depending on the process. |
|
Summarizing and displaying genetic marker information. |
Wide data. |
|
Genome-wide association studies analysis. |
Wide data (for most). |
|
Association tests that are not conducted at the genome level. |
Wide data, with an annotation data set either optional or required, for most. |
|
Estimation of unobserved haplotype frequencies, determination of haplotype from potential trait-influencing markers, and elucidation of markers determinate of haplotype diversity. |
Some are specialized. See individual process descriptions. |
|
Sib-pair chi-square linkage tests. |
A specialized identical-by-descent (IBD) data set and either a pedigree or an annotation data set, depending on the process. |
|
Construction and viewing of linkage maps, quantitative trait loci signal detection, construction of genotype probability data sets, and generation of interval mapping models. |
Either an input cross file or the output file from another process in this subcategory. Some also require an annotation data set. |
|
Summarizing and displaying categorical and quantitative population phenotypes; analysis of multi-environment trial (MET) genotype-by-environment interaction. |
Wide or tall data, depending on the process. |