v291
- v291 Preview 1 - 7 Oct 2013
- v291 Preview 2 - 14 Oct 2013
- v291 Final - 21 Oct 2013
Code changes:
- Fixed ajax code to be tolerant of ISPs that strip newlines from content (#11873). Tim
- Fixed a problem where hub assembly lists were not nicely wrapping on hub portal page (#11889). Tim
- Removed an invalid assert in Gene Haplotypes feature that assumed that if only one haplotype is found, it is the reference haplotype (#11894). Tim
- Rewrote some of makeTrackIndex: replaced mdb and cv access with the lib routines that are much more efficient (#11951). Tim
- Added MAF output in Table Browser for HAL data type (#10637). Brian
- Fixed a bug (and added tests)in pslOpen that would hang on files with only comments. Brian
- Tweaked GWAS otto scripts (#5172). Brian
- Changed "genes" field in gwasCatalog to a longblob from a varchar(255). Brian
- Added maxHours option to genbank load scripts. Currently set to 14 for testing. Brian
- Prioritized list of databases for the genbank process to load (most important ones first). Brian
- Fixed problem on genome-euro that was causing genbank loads to be v-e-r-y slow. Brian
- Made some modifications to support the fact that rrnfs1 is not binary-compatible with hgwdev. Brian
- Fixed Ensembl gene update procedure to properly detect if it's identical to previous version (#11675). Hiram
- Updated build system to automatically detect MySQL libraries and build environment (#11899 #9149). Hiram
- Fixed several bugs in anno* libs found by Case Western team (#11775, #11787). Angie & Jonathan.
- Tweaked search position for Artificial Example Variants (#11110). Angie
- Refined old kludge that affected DGV items at beginning of chrom in Table Browser (#11200). Angie
- Updated links to new Galaxy server from Table Browser (#11898). Angie
- Ongoing work to support HAL and halSnakes in assembly hubs including adding a chromosome color mode for HAL snakes (#10637). Brian
Data changes:
- Added XM, XR RefSeq Gene tracks on hgwdev (#11904). Brian
- Finished 100-way Conservation track documentation (#10272). Hiram
- Reloaded snp138 with allele frequency corrections, include 100% non-reference in Common (#11438, #11954). Angie