Dear Al,

Kindly advise me how to change the colour of the BedGraph file in the histogram 
view in UCSC browser. 
Currently,I am getting a green coloured histogram. My settings are:
color=0,128,0 visiblity=full, which turns out to be greeen.

For individual bedfiles I want to have separate colours like blue and red.
Can you guys suggest me a way of doing that.

Thanks.

Suman

--- On Wed, 9/8/10, Jennifer Jackson <[email protected]> wrote:

> From: Jennifer Jackson <[email protected]>
> Subject: Re: [Genome] conversion of Bedfile to BedGraph problem
> To: "suman pal" <[email protected]>
> Cc: [email protected]
> Date: Wednesday, September 8, 2010, 12:25 AM
> Hello Suman,
> 
> There is a pre-compiled executable available named
> bedItemOverlapCount 
> (same utility as named below, in the forwarded email).
> 
> Ftp from the source downloads area:
> http://hgdownload.cse.ucsc.edu/admin/exe/linux.x86_64/
> 
> If there was some problem that you already encountered with
> the 
> bedItemOverlapCount utility, would you be able to clarify?
> 
> Please continue to use the mailing list [email protected]
> for followup 
> so that our entire team can help contribute to
> troubleshooting the issue.
> 
> Regards,
> 
> Jen
> UCSC Genome Browser Support
> 
> On 9/6/10 10:03 PM, suman pal wrote:
> > Dear All,
> >
> > I need some help in converting the bed file into
> BedGraph.Kindly see the attached bed file and could you
> please send some command lines to process such files and
> visualizing them in UCSC Genome Browser.Please see the
> message below for reference.
> >
> > Sincerely
> > Suman
> >
> >
> > --- On Sat, 9/4/10, suman pal<[email protected]> 
> wrote:
> >
> >> From: suman pal<[email protected]>
> >> Subject: Re: [Genome] Request for ways to
> visualize gff3 Chip on chip data in UCSC browser
> >> To: "Mary Goldman"<[email protected]>
> >> Date: Saturday, September 4, 2010, 11:48 AM
> >> According to your instruction I have
> >> converted a part of my gff3 for chr4 into bed file
> as
> >> nim.bed. However, I am facing difficulty in the
> next step.
> >> i.e. converting it into a BedGraph.
> >> In the directory i have reached the bed item
> overlap count
> >> and downloaded it but I am unable to run it in my
> PC.
> >>
> >> Kindly take a look at the attached file.It will be
> helpful
> >> if you can suggest some steps in more detail.
> >>
> >> sincerely
> >> Suman
> >>
> >> --- On Sat, 9/4/10, Mary Goldman<[email protected]>
> >> wrote:
> >>
> >>> From: Mary Goldman<[email protected]>
> >>> Subject: Re: [Genome] Request for ways to
> visualize
> >> gff3 Chip on chip data in UCSC browser
> >>> To: "suman pal"<[email protected]>
> >>> Cc: [email protected]
> >>> Date: Saturday, September 4, 2010, 3:35 AM
> >>> Hi Suman,
> >>>
> >>> Unfortunately, GFF3 files are not supported as
> custom
> >>> tracks for the
> >>> genome browser. We recommend converting your
> GFF3 file
> >> to a
> >>> bed (more
> >>> information can be found here:
> >>> http://genome.ucsc.edu/FAQ/FAQformat.html#format1).
> >>> Once you have
> >>> converted it you can use the
> bedItemOverlapCount
> >> utility
> >>> (http://hgdownload.cse.ucsc.edu/downloads.html#source_downloads
> >>> in
> >>> "Other executable binary utilities") to build
> a
> >> bedGraph,
> >>> which will
> >>> allow you to see the peaks.
> >>>
> >>> Please feel free to contact the mail list
> again if
> >> you
> >>> require further
> >>> assistance.
> >>>
> >>> Best,
> >>> Mary
> >>> ------------------
> >>> Mary Goldman
> >>> UCSC Bioinformatics Group
> >>>
> >>> On 9/1/10 7:16 AM, suman pal wrote:
> >>>> Dear Sir/madam,
> >>>>
> >>>> I am postdoctoral fellow working in CCMB,
> >>> Hyderabad,India in the laboratory of
> Functional
> >> Genomics and
> >>> Gene Silencing Group.
> >>>>
> >>>> I will be highly obliged if you kindly
> suggest me
> >> some
> >>> steps to display my gff3 Nimblegen ChIP on
> Chip
> >> genome
> >>> tiling array files in the UCSC genome
> Browser.The
> >> organisms
> >>> is Drosophila Melanogaster (dm3 rel5).
> >>>>
> >>>> When I am adding the gff3 files in custom
> track
> >> the
> >>> track is looking inverted to me. Is there any
> way to
> >> change
> >>> this view.
> >>>>
> >>>> Most importantly Is there any way I can
> display
> >> the
> >>> peak scores or log2 ratios as well.
> >>>>
> >>>>
> >>>> Looking forward to your reply.
> >>>>
> >>>> Sincerely,
> >>>> Suman Pal,
> >>>> Laboratory for Gene Silencing and
> Functional
> >> Genomics
> >>>> G-110, South wing, ground floor,
> >>>> CCMB,Hyderabad,India
> >>>>
> >>>>
> >>>>
> >>>>
> _______________________________________________
> >>>> Genome maillist  -  [email protected]
> >>>> https://lists.soe.ucsc.edu/mailman/listinfo/genome
> >>>>
> >>>
> >>
> >>
> >>
> >
> >
> >
> >
> >
> >
> > _______________________________________________
> > Genome maillist  -  [email protected]
> > https://lists.soe.ucsc.edu/mailman/listinfo/genome
> 


      

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