[GSoC] GSOC project: improve SegAnnDB interactive DNA copy number analysis
Eric Talevich
eric.talevich at gmail.com
Tue Mar 4 20:45:28 UTC 2014
Hi Toby,
The project idea looks good to me so far. If you feel confident in the
proposal now, would you mind posting it on the OBF wiki page under the
"cross-project" section?
http://www.open-bio.org/wiki/Google_Summer_of_Code_2014_Ideas
Thanks,
Eric
On Tue, Mar 4, 2014 at 9:16 AM, Toby Hocking <tdhock5 at gmail.com> wrote:
> Thanks for the ideas and the link to the Galaxy information, Peter. For
> now it looks difficult to implement interactively defining and saving
> annotated regions as a Galaxy Visualization, but I added Galaxy integration
> the list of TODOs, and to the list of possible improvements that the GSOC
> student could implement.
>
> About the Python/C/C++ segmentation modules, they are indeed only Python 2
> at the moment, and I just created some end user documentation
>
>
> https://r-forge.r-project.org/scm/viewvc.php/*checkout*/python/00_README.html?revision=32&root=segannot
>
>
> On Tue, Mar 4, 2014 at 5:13 AM, Peter Cock <p.j.a.cock at googlemail.com>wrote:
>
>> On Mon, Mar 3, 2014 at 10:13 PM, Toby Hocking <tdhock5 at gmail.com> wrote:
>> > Hey Eric thanks for your input -- these are really valuable comments!
>> >
>> > It would be nice to integrate with Galaxy, but do you think the
>> interactive
>> > features would be possible? Can you recommend the relevant part of the
>> > Galaxy manual to read?
>>
>> I've not tried this, but see
>> https://wiki.galaxyproject.org/VisualizationsRegistry
>> and for a (slightly out of date) overview, Jeremy's slides from BOSC 2012:
>>
>> http://www.slideshare.net/jandot/j-goecks-the-galaxy-visual-analysis-framework
>>
>> > I agree that it should be very nice to have a more robust genome viewer
>> to
>> > view other tracks such as RefSeq genes or SNP allele frequency data, but
>> > again I wonder if the interactive annotation would be possible? By the
>> way,
>> > what is "paging GMOD?"
>>
>> I guess Eric meant paging as in calling (for some reason pagers
>> were very popular in the USA before mobile phones took off).
>> http://en.wikipedia.org/wiki/Pager
>>
>> The verb is also used in large buildings for Tannoy announcements
>> via ceiling speakers ("Could Mr Jones please come to reception").
>> Although they probably don't use Tannoy as a noun in the USA?
>> http://en.wikipedia.org/wiki/Tannoy
>>
>> > By the way, the reason why I decided to draw the signal using PNG
>> > scatterplots is because it is very fast -- at first I tried using
>> > JavaScript/D3 to draw it as SVG <circle> elements, but that is really
>> slow
>> > when there are a lot of points on screen (as in the genome-wide plots).
>> >
>> > There is some SegAnnDB code for reading bedGraph files from disk before
>> they
>> > are loaded into BerkeleyDB --- do you think that reader is suitable for
>> > inclusion in BioPython?
>> >
>> > Finally, there are indeed some Python extension modules (PrunedDP and
>> > SegAnnot) for efficiently calculating the displayed segmentation
>> models, so
>> > those could definitely be included in BioPython if you like. Their
>> source
>> > code is in SVN here
>> > https://r-forge.r-project.org/scm/viewvc.php/python/?root=segannot
>>
>> Interesting - a Python module written entirely in C code (not sure
>> but I suspect for Python 2 only at the moment). Is there some end
>> user documentation to help understand the intended usage?
>>
>> Regards,
>>
>> Peter
>>
>
>
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