Hello Tiandao,

Try these two modifications:
1) remove the track line from the file
2) leave off all arguments to the sort command (the numerical sort is 
not wanted)

sort bedFile.bed | bedItemOverlapCount [options] <database> stdin

A new assembly requires the six files listed in this help document:
http://genomewiki.ucsc.edu/index.php/Minimal_Browser_Installation

It would be OK to skip step #10 in this help document:
http://genomewiki.ucsc.edu/index.php/Building_a_new_genome_database

Thanks,

Jen
UCSC Genome Browser Support

On 7/13/10 12:19 PM, Tiandao Li wrote:
> Hi Jen,
>
> However, it still showed the wrong mesg. The file is tab separated.
>
> $ more ccmv.bed
> track color=125,0,0
> NC_003521    6664    7191    RL10
> NC_003521    7202    7900    RL11
> NC_003521    7939    9021    RL12
> NC_003521    9123    10124    RL13
> NC_003521    9123    10124    RL13
> NC_003521    10256    10432    UL2
> NC_003521    10504    11097    UL4
> NC_003521    11469    11924    UL5
> NC_003521    12130    12981    UL6
> NC_003521    13052    13693    UL7
> NC_003521    13799    14305    UL8
>
> $ sort -k1,1 -k2,2n ccmv.bed | /opt/kent/bedItemOverlapCount ccmv stdin
> Expecting 3 words line 12 of stdin got 2
>
> And would you explain why need to generate gc5Base data and load table
> during building custom geome db?
>
> Thanks,
>
> Tiandao
>
> On Tue, Jul 13, 2010 at 1:55 PM, Jennifer Jackson <[email protected]
> <mailto:[email protected]>> wrote:
>
>     Hello Tiandao,
>
>     Use the database name that you assigned to your reference genome
>     when it was loaded. This is the same value as in
>     "hgcentral.dbDb.name <http://hgcentral.dbDb.name>".
>
>     Hopefully this helps,
>
>
>     Jen
>     UCSC Genome Browser Support
>
>     On 7/13/10 8:33 AM, Tiandao Li wrote:
>
>         Hi Jen,
>
>         I have no problem to create and load trackDb. I want to use BED
>         for our
>         genome annotation. The following is my bed file.
>
>         $ more ccmv.bed
>         track name=CMV color=125,0,0
>         NC_003521    6664    7191     RL10
>         NC_003521    7202    7900     RL11
>         NC_003521    7939    9021     RL12
>         NC_003521    9123    10124     RL13
>         NC_003521    9123    10124     RL13
>         NC_003521    10256    10432     UL2
>         NC_003521    10504    11097     UL4
>         NC_003521    11469    11924     UL5
>         NC_003521    12130    12981     UL6
>         NC_003521    13052    13693     UL7
>         NC_003521    13799    14305     UL8
>         NC_003521    14327    14860     UL9
>
>
>         sort -k1,1 -k2,2n bedFile.bed \
>               | bedItemOverlapCount [options] <database> stdin \
>                   | wigEncode stdin data.wig data.wib
>
>         However, I didn't know which database I should input for
>         bedItemOverlapCount. Or any alternative method directly convert
>         bed to
>         wig, which I knew how to upload.
>
>         Thanks,
>
>         Tiandao
>
>         On Mon, Jul 12, 2010 at 11:02 PM, Jennifer Jackson
>         <[email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>> wrote:
>
>             Hello Tiandao,
>
>             The README file I pointed you to has the instructions for
>         creating a
>             track. Did you have a question about a particular step?
>
>             Or maybe the problem is related to track type? The RefSeq Genes
>             track type is "genePred". It might be good to examine the
>         current
>             hg19 trackDb.ra file in the kent source tree to see how
>         RefSeq Genes
>             is set up there.
>
>             Or maybe the problem is understanding the viewing options? A
>         PSL,
>             BED, and genePred track type all look a bit similar in the
>         browser
>             display. Dense mode will put all data on the same line. Both
>         pack
>             and full will display one line per table/file (where one line
>             usually represents the alignment of a entire sequence). To
>         see this,
>             open the RefSeq Gene track in the browser and switch between the
>             different display modes using the pull-down menu under the
>         track name.
>
>             Some display help:
>         http://genome.ucsc.edu/goldenPath/help/hgTracksHelp.html#FineTuning
>
>             Hopefully this helps, but if not please let us know.
>
>             Best regards,
>
>             Jen
>             UCSC Genome Browser Support
>
>             On 7/12/10 8:40 AM, Tiandao Li wrote:
>
>                 Hi,
>
>                 I searched through genome and genome-mirror lists about
>         how to add
>                 annotation info (such as CDS) to genome database on local
>                 mirror. Where
>                 can I find actual examples of trackDb.ra to load
>         annotation info to
>                 local mirror?
>
>                 Thanks,
>
>                 Tiandao
>
>                 On Tue, Jul 6, 2010 at 4:38 PM, Jennifer Jackson
>         <[email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>
>         <mailto:[email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>>> wrote:
>
>                     Hi Tiandao,
>
>                     For genomes with annotation, the path would be:
>
>                     1) load the reference genome sequence as you have done
>                 previously
>                     2) layer in annotation as tracks mapped to the
>         genome in #1
>
>                     This README in the kent source tree has the details
>         for #2
>                     kent/src/product/README.trackDb
>
>                     I hope this pointer is useful, but please let us
>         know if you
>                 need
>                     more help.
>
>                     For next time, it would nice for us if you sent your
>         question
>                     through one our mailing lists. This question would
>         be a good
>                 fit for
>                     the [email protected]
>         <mailto:[email protected]>
>         <mailto:[email protected]
>         <mailto:[email protected]>>
>         <mailto:[email protected]
>         <mailto:[email protected]>
>         <mailto:[email protected]
>         <mailto:[email protected]>>>
>
>                     list. Doing this would help us to get you a speedy
>         answer
>                 and also
>                     help other users that are reviewing the Q & A on the
>         public
>                 posting.
>                     If you need private (not posted) communications, the
>         list
>         [email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>
>         <mailto:[email protected] <mailto:[email protected]>
>         <mailto:[email protected]
>         <mailto:[email protected]>>> would be an
>
>                     alternative as it is internal to the UCSC Browser
>         team only.
>
>                     Best regards,
>                     Jen
>
>                     UCSC Genome Browser Support
>         http://genome.ucsc.edu/contacts.html
>         [email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>
>         <mailto:[email protected] <mailto:[email protected]>
>         <mailto:[email protected] <mailto:[email protected]>>>
>
>         [email protected] <mailto:[email protected]>
>         <mailto:[email protected]
>         <mailto:[email protected]>>
>         <mailto:[email protected]
>         <mailto:[email protected]>
>         <mailto:[email protected]
>         <mailto:[email protected]>>>
>
>
>
>                     On 7/6/10 1:00 PM, Tiandao Li wrote:
>
>                         Hi Jen,
>
>                         We have several annotated genomes of viruses
>         download
>                 from NCBI and
>                         other DB serves. Now I want to import them with
>                 annotation into our
>                         local genome browser. Would you please point me
>         to the
>                 details
>                         of how to
>                         do it? I import some sequences without
>         annotation to our
>                 browser
>                         before.
>
>                         Thanks,
>
>                         Tiandao
>
>
>
>
_______________________________________________
Genome maillist  -  [email protected]
https://lists.soe.ucsc.edu/mailman/listinfo/genome

Reply via email to