Hi Tiandao, This could be a set-up problem in hgcentral if you assigned one of your loaded databases to the clade "Other". Were the defaultDb and genomeClade tables modified as in step #12 of this help wiki?
http://genomewiki.ucsc.edu/index.php/Building_a_new_genome_database Thank you, Jen UCSC Genome Browser Support On 7/16/10 10:24 AM, Tiandao Li wrote: > Hi Jen, > > Finally I imported all genomes and annotation files into local genome > browser. However, when select Other (clade), the page always show the > error mesg. Would you please what caused this error, and how to fix it? > Thanks! > > > *Error(s):* > > * Error reading 5 bytes: Operation not permitted > > > On Thu, Jul 15, 2010 at 12:04 AM, Jennifer Jackson <[email protected] > <mailto:[email protected]>> wrote: > > Hello Tiandao, > > Are you still having trouble with your mirror? I am not sure which > problems were sorted out already and which you would still like help > with. > > For your track below, have you tried setting the display to "pack" > or "full" in the assembly browser display? To do this, use the pull > down menu under the track name. > > More display help: > > http://genome.ucsc.edu/goldenPath/help/hgTracksHelp.html#FineTuning > > File format help (including .wig): > http://genome.ucsc.edu/FAQ/FAQformat.html > > Regarding the trackDb table - this is required. Lines in the table > correspond to tracks in the assembly. > > > Hopefully this helps, > > Jen > UCSC Genome Browser Support > > On 7/14/10 9:29 AM, Tiandao Li wrote: > > Hi Jen, > > I figured out a way to import bed file into DB. Please look at > the table > below. > > *Sample Rows * > > > > bin chrom chromStart chromEnd name score > strand > 585 NC_003521 6664 7191 RL10 1000 + > 585 NC_003521 7202 7900 RL11 1000 + > 585 NC_003521 7939 9021 RL12 1000 + > 585 NC_003521 9123 10124 RL13 1000 + > 585 NC_003521 9123 10124 RL13 1000 + > 585 NC_003521 10256 10432 UL2 1000 + > 585 NC_003521 10504 11097 UL4 1000 + > 585 NC_003521 11469 11924 UL5 1000 + > 585 NC_003521 12130 12981 UL6 1000 + > 585 NC_003521 13052 13693 UL7 1000 + > > > The problem is I can't show the name next to the bar. Please help! > > On Wed, Jul 14, 2010 at 10:32 AM, Tiandao Li <[email protected] > <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> wrote: > > Hi Jen, > > I followed your advice, however, the converted wig file > contains no > annotated info, such as RL10 in the last column. > > Regarding gc5Base generation in building new genome, from > the help > manual, looks like it needs at least one trackDb to show the > genome. > Is there a way to check on the genome on browser without any > trackDb, anyway, there are 3 default trackDbs there, Base > Position, > Short Match, and Restr Enzymes. > > Thanks, > > Tiandao > > > On Tue, Jul 13, 2010 at 4:48 PM, Jennifer Jackson > <[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> wrote: > > 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]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[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> > <http://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]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[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]>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> > <mailto:[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]>>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>>>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>>> > <mailto:[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]>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> > <mailto:[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]>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>> > <mailto:[email protected] <mailto:[email protected]> > <mailto:[email protected] <mailto:[email protected]>>> > <mailto:[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]>>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>>>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>> > <mailto:[email protected] > <mailto:[email protected]> > <mailto:[email protected] > <mailto:[email protected]>>> > <mailto:[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
