Processing CEL files
Normalizes and computes relative expressions for all CEL files in work directory
ProcessCels(threshold.over=1.5,threshold.under=(2/3),remove_method=1,
local_file=NULL)
1
,
will keep 1 probeset with the following priority:
1): nnn_at
;
2): nnn_a_at
;
3): nnn_s_at
;
4): nnn_x_at
;
5): lowest nnn
if multiple probes still existIf remove_method=2
, probesets will only be removed if
several probesets of the same gene map to the exact same location.
In the case that many probesets map to the same location, one probeset
will be retained according to the priority of option 1 above.
If remove_method=0
, no multiple probesets will be removed
"ID"
(Affy ID number);
2): "Sym"
(gene Symbol);
3): "Value"
(Expression values);
4): "LogRel"
(Relative expressions);
5): "Loc"
(Chromosomal locations);
6): "Chr"
(Chromosome number);
7): "Band"
(Cytoband);
8): "Arm"
(Chromosomal arm)this function uses the RMA algorithm to normalize *.CEL files in work directory. It then computes relative expressions for every probe on every sample. Locations for probesets are downloaded from UCSC, as the standard BioConductor annotations do not map probeset location (they only map the location to the corresponding gene). Multiple probesets belonging to the same gene are removed as described above. The function then determines which probes are overexpressed and underexpressed relative to the median probeset values across all samples. Finally,the relative expressions are log2-transformed.
## Not run:
# data <- ProcessCels()
# ## End(Not run)
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