[BioC] Identification of unannotated transcripts using Arabidopsis 1.0R Tiling Arrays
Wolfgang Huber
huber at ebi.ac.uk
Tue Jul 10 10:35:31 CEST 2007
Dear Pia,
to supplement Sean's suggestion, you could look at the two papers cited
here: http://www.ebi.ac.uk/huber-srv/queryGene
The analysis for this project was done with the tilingArray package. But
applying this to your data will require a substantial amount of your own
programming, due to the variety of tasks, the tilingArray package does
not provide an easy to use end-to-end it solution; just some buiding
blocks. Still, of course, I hope that it is useful, let me know if you
have questions.
Best wishes
Wolfgang
------------------------------------------------------------------
Wolfgang Huber EBI/EMBL Cambridge UK http://www.ebi.ac.uk/huber
Sean Davis ha scritto:
> Pia Sappl wrote:
>> Dear Tiling Array Users
>>
>> We have recently performed an Arabidopsis Tiling Array experiment to
>> assess differential expression between mock treated and dex treated
>> samples at 4 and 12 h after dex treatment (2 biological paired
>> replicates = 8 chips in total). ie mock 4h versus dex 4 h and mock 12 h
>> vs dex 12 h. As part of our analysis we would like to identify regions
>> of DNA that do not fall within annotated exons (ie unannotated genes).
>> Is anyone aware of an existing R algorithm we could use (or perhaps with
>> minimal modifications) that would do this? So far we have used TAS
>> (Affymetrix software) to normalise the data and define regions of
>> positive expression. We have also used IGB (Affymetrix genome browser)
>> to manually inspect the results. However, we would like to take a more
>> automated and objective approach using R. Finally, has anyone used the
>> Tiling Array to identify differential expression? And if so, what
>> approach was used?
>>
> I haven't used the package in a long time, but you might look at the
> tilingArray package. Also, I would highly recommend reading some of the
> literature utilizing tiling arrays. The analysis of such arrays is full
> of challenges and will probably require some customized analyses to
> answer specific biologic questions.
>
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