File:UcscLinks.xls
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Revision as of 21:05, 17 June 2011 by Kuhn (talk | contribs) (uploaded a new version of "File:UcscLinks.xls": Adjusted links to new tableName for OMIM tracks in the links.)
UcscLinks.xls (file size: 13 KB, MIME type: application/zip)
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spreadsheet to create links that open Genome Browser views when a user types in a variety of entries, including genomic coordinates, gene names or chromosome bands.
File history
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(newest | oldest) View (newer 10 | older 10) (10 | 20 | 50 | 100 | 250 | 500)| Date/Time | Dimensions | User | Comment | |
|---|---|---|---|---|
| 23:27, 11 May 2011 | (22 KB) | Kuhn (talk | contribs) | Reverted to version as of 23:08, 11 May 2011 | |
| 23:11, 11 May 2011 | (22 KB) | Kuhn (talk | contribs) | trying this again.... | |
| 23:08, 11 May 2011 | (22 KB) | Kuhn (talk | contribs) | retried upload. ran into problem with capital U in file name. It kept taking the one with lower-case u instead by mistake. | |
| 23:05, 11 May 2011 | (22 KB) | Kuhn (talk | contribs) | added comment about 2-SNP range query. | |
| 22:15, 9 May 2011 | (22 KB) | Kuhn (talk | contribs) | ||
| 19:29, 29 November 2010 | (24 KB) | Kuhn (talk | contribs) | spreadsheet to create links that open Genome Browser views when a user types in a variety of entries, including genomic coordinates, gene names or chromosome bands. | |
| 19:25, 29 November 2010 | (23 KB) | Kuhn (talk | contribs) | Reverted to version as of 00:02, 25 November 2010 | |
| 19:25, 29 November 2010 | (24 KB) | Kuhn (talk | contribs) | spreadsheet to create links that open Genome Browser views when a user types in a variety of entries, including genomic coordinates, gene names or chromosome bands. | |
| 05:38, 25 November 2010 | (24 KB) | Kuhn (talk | contribs) | spreadsheet to create links that open Genome Browser views when a user types in a variety of entries, including genomic coordinates, gene names or chromosome bands. | |
| 00:02, 25 November 2010 | (23 KB) | Kuhn (talk | contribs) | spreadsheet to create links that open Genome Browser views when a user types in a variety of entries, including genomic coordinates, gene names or chromosome bands. |
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