| data:probeAnno {davidTiling} | R Documentation |
The environment contains probe mapping information for the Affymetrix Scerevisiaetiling chip from 2004, which was custom-made for the Stanford Genome Center. The chips tile the complete genome of S. cerevisiae in steps of 8 bases, separately for each strand of each chromosome. The two tiles for one chromosome (Watson and Crick strands) are offset by 4 bases.
In the following a brief description of the 138 elements of the
probeAnno environment.
probeReverse: a list of 8 factors, each of length 6553600,
corresponding to the rows of davidTiling. For
example, if the probe corresponding to the j-th row
in davidTiling maps to the
coding sequence of a gene, then the factor level of
probeRevers$CDS[j] is the name of the gene, and the empty string
"" otherwise. This applies to samples that were hybridized to
the chip after a reverse transcription step.
probeDirect: analogous to probeReverse, but for samples
that were hybridized to the chip without a reverse transcription step.
The probes map to the opposite chromosomal strand compared to
experiments with reverse transcription.
1.+.index: indices (from 1...6553600, corresponding to the
rows of davidTiling) of probes mapping to the Watson
strand of chromosome 1.
1.+.start, 1.+.end: start and end positions in genomic
coordinates of the alignments of the probes (in the same order as in
1.+.index) to the Watson strand of chromosome 1. For 25-mers,
the values in 1.+.end are those in 1.+.start plus 24, but
not all probes on the array are 25-mers.
1.-.unique: specificity of the probe:
1.-.index, 1.-.start, 1.-.end, 1.-.unique:
analogous to the above, but for the Crick strand of chromosome 1.
2.+.index, 2.+.start, 2.+.end, 2.-.unique:
analogous to the above, but for the Watson strand of chromosome 2;
and so forth. "Chromosome 17" is mitochondrial DNA.
data("probeAnno")
W. Huber huber@ebi.ac.uk
Probe sequences were obtained from Affymetrix in a file called
S.cerevisiae_tiling.1lq.
The genomic sequences of the S. cerevisiae chromosomes were
downloaded from
ftp://genome-ftp.stanford.edu/pub/yeast/data_download/sequence/genomic_sequence/chromosomes/fasta
on 7 Aug 2005, 18:16 BST in 17 files
chr01.fsa–chr16.fsa, and chrmt.fsa.
The probe sequences were matched against the chromosomal sequencences
with the program MUMmer, see the script
mapProbesToGenome.sh (in the inst/scripts directory of this
package). MUMmer results were parsed and processed into the
probeAnno environment with the script
makeProbeAnno.R (in the inst/scripts directory of this package).
data("probeAnno")
ls(probeAnno)
str(probeAnno$"1.+.start")