1-DAV-202 Data Management 2023/24
Previously 2-INF-185 Data Source Integration
Difference between revisions of "Genomika: Rozvojové projekty"
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** From several overlapping matches keep only the strongest (try tool overlapSelect) | ** From several overlapping matches keep only the strongest (try tool overlapSelect) | ||
** More ambitious: Explore creating image of each RNA structure and somehow linking it to the info page for the match (as in non-coding RNA track in the human genome browser - see for example http://genome-euro.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr1%3A16520585%2D16520658, display non-coding RNA track and click on the tRNA match) | ** More ambitious: Explore creating image of each RNA structure and somehow linking it to the info page for the match (as in non-coding RNA track in the human genome browser - see for example http://genome-euro.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr1%3A16520585%2D16520658, display non-coding RNA track and click on the tRNA match) | ||
+ | |||
+ | ===Information for users=== | ||
+ | * Each track should provide basic information for users in the HTML document displayed after clicking on track name or left bar of the browser image. | ||
+ | * The information should summarize what is displayed, what was source of the data, what program was used to produce the results etc | ||
+ | ** keep it less technical, with a link to your github wiki page for the track for potential developers replicating your work | ||
+ | * See examples for tracks on the http://genome-euro.ucsc.edu/ browser | ||
+ | * Also, the genome as a whole should have a description page. On the title page of http://genome-euro.ucsc.edu/ you see details of the selected assembly, e.g. for the guinea pig genome you see text | ||
+ | <pre> | ||
+ | Guinea pig Genome Browser - cavPor3 assembly | ||
+ | The Feb. 2008 Cavia porcellus draft assembly (Broad Institute cavPor3) was produced by the Broad Institute at MIT and Harvard. | ||
+ | ... | ||
+ | </pre> | ||
+ | * You should create some explanatory text for you species and genome and make it display on the title page | ||
+ | ** This already works for Yarrowia lipolitica on genomika server, so you can try to find out how it was done | ||
+ | |||
+ | ==MalSym group== | ||
+ | |||
+ | ===Clickable genes=== | ||
+ | * If you click on a gene or other displayed item in a well-setup genome browser, you get a page with more information about this item | ||
+ | * This does not work satisfactorily on our genomika browser | ||
+ | * Look at all tracks displaying gene information in four browsers: | ||
+ | ** sacCer3 in original UCSC genome browser [http://genome-euro.ucsc.edu/cgi-bin/hgTracks?db=sacCer3], tracks NCBI RefSeq, SGD Genes, Ensembl Genes | ||
+ | ** sacCer3 in our genomika genome browser [http://genomika.compbio.fmph.uniba.sk/cgi-bin/hgTracks?db=sacCer3], tracks | ||
+ | ** yarLip1 in our genomika genome browser [http://genomika.compbio.fmph.uniba.sk/cgi-bin/hgTracks?db=yarLip1], tracks Ens. Genes (L), RefSeq Genes (L) | ||
+ | ** malSym1 in our genomika genome browser [http://genomika.compbio.fmph.uniba.sk/cgi-bin/hgTracks?db=malSym1], track | ||
+ | * For each explored track find out what gets displayed after clicking at a gene, whether there are any error messages, whether the page contains a link to the source database (e.g. Ensembl, RefSeq, NCBI, SGD) | ||
+ | * | ||
+ | |||
===Information for users=== | ===Information for users=== |
Revision as of 08:18, 12 April 2018
Contents
MalGlo group
User trackDb, code management
- Think how to better manage changes to browser code in the future instances of the course
- Explore possibilities of each user having their own trackDb
- Start by reading short info in /kentsrc/trackDb/makefile on genomika server
# Browser supports multiple trackDb's so that individual developers # can change things rapidly without stepping on other people's toes. ...
- Write a manual how to do your suggested changes and test it
Rfam
- Rfam http://rfam.xfam.org/ is a database of families of non-coding RNAs
- It contains a covariance model for each family
- The database can be downloaded and searched against a genome using Infernal tool http://eddylab.org/infernal/
- Do this search, then convert the output to appropriate format and display in the browser
- Possibly use BEDdetail format https://genome.ucsc.edu/FAQ/FAQformat.html#format1.7
- After clicking on an Rfam match, there should be some display of additional information about the match and a link to the Rfam database. You can achieve this by the following lines in trackDb.ra:
type bedDetail 14 url http://rfam.xfam.org/family/$$ urlLabel Rfam:
Example of BEDdetail format for a Rfam match (items should be tab-separated, the last column starts at "truncated:")
chrom chromStart chromEnd name score strand thickStart thickEnd reserved blockCount blockSizes chromStarts id description contigA 75109 75380 Fungi_SRP-1 1002 - 75109 75109 0 1 271 0 RF01502 truncated: no, E-value: 3.5e-19
- Further things which you might want to explore:
- Remove matches that correspond to tRNAScan-SE matches (try tool overlapSelect)
- From several overlapping matches keep only the strongest (try tool overlapSelect)
- More ambitious: Explore creating image of each RNA structure and somehow linking it to the info page for the match (as in non-coding RNA track in the human genome browser - see for example http://genome-euro.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr1%3A16520585%2D16520658, display non-coding RNA track and click on the tRNA match)
Information for users
- Each track should provide basic information for users in the HTML document displayed after clicking on track name or left bar of the browser image.
- The information should summarize what is displayed, what was source of the data, what program was used to produce the results etc
- keep it less technical, with a link to your github wiki page for the track for potential developers replicating your work
- See examples for tracks on the http://genome-euro.ucsc.edu/ browser
- Also, the genome as a whole should have a description page. On the title page of http://genome-euro.ucsc.edu/ you see details of the selected assembly, e.g. for the guinea pig genome you see text
Guinea pig Genome Browser - cavPor3 assembly The Feb. 2008 Cavia porcellus draft assembly (Broad Institute cavPor3) was produced by the Broad Institute at MIT and Harvard. ...
- You should create some explanatory text for you species and genome and make it display on the title page
- This already works for Yarrowia lipolitica on genomika server, so you can try to find out how it was done
MalSym group
Clickable genes
- If you click on a gene or other displayed item in a well-setup genome browser, you get a page with more information about this item
- This does not work satisfactorily on our genomika browser
- Look at all tracks displaying gene information in four browsers:
- For each explored track find out what gets displayed after clicking at a gene, whether there are any error messages, whether the page contains a link to the source database (e.g. Ensembl, RefSeq, NCBI, SGD)
Information for users
- Each track should provide basic information for users in the HTML document displayed after clicking on track name or left bar of the browser image.
- The information should summarize what is displayed, what was source of the data, what program was used to produce the results etc
- keep it less technical, with a link to your github wiki page for the track for potential developers replicating your work
- See examples for tracks on the http://genome-euro.ucsc.edu/ browser
- Also, the genome as a whole should have a description page. On the title page of http://genome-euro.ucsc.edu/ you see details of the selected assembly, e.g. for the guinea pig genome you see text
Guinea pig Genome Browser - cavPor3 assembly The Feb. 2008 Cavia porcellus draft assembly (Broad Institute cavPor3) was produced by the Broad Institute at MIT and Harvard. ...
- You should create some explanatory text for you species and genome and make it display on the title page
- This already works for Yarrowia lipolitica on genomika server, so you can try to find out how it was done