Description Usage Arguments Details Value Author(s) References See Also Examples
recoverAllNameGroups
recovers, from a metagroup, the
names of the genes part of an identified mutually exclusive group.
1 | recoverAllNamesGroups(groupsMeta, clGenes)
|
groupsMeta |
list containing groups of equivalent genes, as returned
by the field |
clGenes |
matrix of mutually exclusive groups of same size, as gene
names. This type of matrix is returned by either |
This function can be used if the input binary matrix contains
identical events that need to be merged into metagenes using
doMetagene
. Running recoverAllNamesGroups
provides the
set of identical alterations which are part of the identified mutually
exclusive groups.
In order to run this function on all the identified mutually exclusive
groups as returned by TiMEx
or
findSignifCliques
, it is necessary to run it separately on
each matrix element (corresponding to different group sizes and different
correction methods) of the genesSignif
field in the structure
returned by either TiMEx
or findSignifCliques
.
For example, after loading data(ovarianGroups)
and
data(ovarianOutput)
, and running
rGroups<-recoverAllNamesGroups(ovarianGroups,
signifGroups$genesSignif[[3]]$bonf)
rGroups[[14]]
has 3 elements (as many as genes part
of the identified mutually exclusive groups). Each element is the metagroup
of each of the genes part of the 14th mutually exclusive group in the input
matrix
signifGroups$genesSignif[[3]]$bonf
. Namely, BRD4-CNA and
MYC-CNA have unique alteration patterns among samples, and are alone
in their metagroup, while CASC1-CNA has an identical alteration
pattern with KRAS-CNA and LYRM5-CNA. The numbers
below the gene names are the indices of the genes in the initial input
binary matrix of patients.
list with as many elements as number of identified mutually exclusive groups, i.e. number of rows in the input matrix. Each of its elements is further a list, containing, at each position, the metagroup of the genes in the initial group at that resepective position. For an example, see Details above.
Simona Cristea, scristea@jimmy.harvard.edu
Constantinescu et al.: TiMEx: A Waiting Time Model for Mutually Exclusive Cancer Alterations. Bioinformatics (2015).
doMetagene
for collapsing the genes of an input
matrix with identical alteration patterns into metagroups.
1 2 3 | data(ovarianGroups)
data(ovarianOutput)
r<-recoverAllNamesGroups(ovarianGroups,ovarianOutput$genesSignif[[3]]$bonf)
|
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