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sabrina.shao
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220
@sabrinashao-1661
Last seen 10.2 years ago
Hi, all
I don't know if it is just by chance, I was retrieving sequence for
ENSMUST00000027587<http: www.ensembl.org="" mus_musculus="" transcript="" exon="" s?g="ENSMUSG00000026349;t=ENSMUST00000027587">using
BSgenome
the coordinate I use was what I retrieved from UCSC through following
code:
library(rtracklayer)
session <- browserSession()
genome(session) <- "mm9"
q2<- ucscTableQuery(session,"
ensGene")
ensGene<-getTable(q2)
the result is:
name name2 chrom strand txStart txEnd
980 NM_028399 Ccnt2 chr1 + 129670740 129701414
exonStarts
980
129670740,129671677,129688181,129689934,129691831,129694417,129695966,
129698182,129698738,
exonEnds exonCount
980
129670962,129671759,129688310,129689995,129691894,129694463,129696130,
129698253,129701414,
9
But from Ensembl or even UCSC genome browser, the first exon
coordinate
starts at 129670741, so there is 1 bp shift. Because of that, I can't
get
the right sequence that I need. So there is anyway to correct that or
am I
missing some steps? Thanks!
Sabrina
--
Sabrina
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