Changes between Version 4 and Version 5 of net.sf.basedb.reggie/notes423
- Timestamp:
- Sep 4, 2019, 8:58:07 AM (5 years ago)
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net.sf.basedb.reggie/notes423
v4 v5 1 1 = Updating to Reggie 4.23 = 2 2 3 TODO - when to do the different steps! 3 ---- 4 **IMPORTANT! ** \\ 5 This update requires a lot of manual work to install. Some things should be prepared in advance and some things should be 6 done after Reggie 4.23 has been installed. Make sure to assign enough time for the update. No-one should be working with 7 registrations and other things during the upgrade since some wizards may not work correctly until the update has been completed. 8 It is also important to no secondary analysis jobs are running, since this may cause the results to be incorrectly registered 9 or not registered at all. 10 ---- 4 11 5 TODO - state requirements: no current sequencing or secondary analysis jobs 12 == 1. New pipeline scripts == 6 13 7 == 1. Set value for Pipeline annotation on existing items == 14 There are new pipeline scripts: http://baseplugins.thep.lu.se/browser/other/pipeline/trunk 15 Download and install at a suitable location on the prime cluster. 8 16 9 Almost all existing items from Library and downstream must be given a value for the **Pipeline** annotation. The table below specifies the value 17 == 2. Changes in reggie-config.xml == 18 19 There are several changes in reggie-config.xml: 20 21 * The path to the pipeline scripts must be changed to point to the new version. 22 * The path to Picard must be changed to a newer version: `/usr/local/packages/picard-tools/2.20.0`. 23 * A new section for the MIPs demux has been added `<demux-mips>`. The default parameters can probably be used. 24 * The parameter syntax for Picard has been changed. The old syntax `key=value` has been changed to `-key value`. This affects several 25 existing configuration settings: 26 - `<demux>/<extract-options>` 27 - `<demux>/<fastq-options>` 28 - `<align>/<mark-duplicates-options>` 29 - `<align-hisat>/<mark-duplicates-options>` 30 31 32 == 3. Install Reggie 4.23 and run the installation wizard == 33 34 35 == 4. Set a value for the Pipeline annotation on existing items == 36 37 Almost all existing items from **Library** and downstream must be given a value for the **Pipeline** annotation. The table below specifies the value 10 38 to set for the Pipeline annotation for different types of items. It should be possible to do a manual batch export/import for each row or groups of rows. 11 39 … … 21 49 || Software || Demuxing, Merging || - || RNAseq || 22 50 23 == 2. Other updates to existing items ==51 == 5. Other updates to existing items == 24 52 25 Existing Hardware items of type=Sequencershould be updated with a value for the **!FlowCellType** annotation. It should be either !NextSeq or !HiSeq.53 Existing **Hardware** items of type=**Sequencer** should be updated with a value for the **!FlowCellType** annotation. It should be either !NextSeq or !HiSeq. 26 54 27 == 3. New items that should be created ==55 == 6. New items that should be created == 28 56 29 57 || **Item type** || **Subtypes** || **Additional settings** || **Comment** || … … 36 64 || Software || Merging || Pipeline=MIPs || One or more software entries that will appear in the MIPs demux wizard (merge section) || 37 65 38 == 4. Barcode templates ==66 == 7. Barcodes and barcode template plates == 39 67 40 68 Most of the barcode information (such as the sequences, positions, etc.) should be available as a file that can be used with batch importers. Some steps need to be done manually. 41 69 42 1. A barcode templates is represented as a **Bioplate** item where each coordinate is linked to a **Tag** item. Start by manually creating the required number of bioplates. They should have the following values: 43 44 || **Bioplate type** || !BarcodeTemplate || 45 || **Plate geometry** || 96-well (8x12) || 46 || **Pipeline** (annotation) || MIPs || 47 48 49 2. Import/create **Tag** items from file using the batch **Tag importer** and then add annotations with the **Annotation importer**. The following values are required: 70 1. Import/create **Tag** items from file using the batch **Tag importer** and then add annotations with the **Annotation importer**. The following values are required: 50 71 51 72 || **Name** || Name of the barcode/tag which must be unique || … … 53 74 || **!BarcodeSequence** || The barcode sequence for the first index read || 54 75 || **BarcodeSequence2** || The barcode sequence for the second index read || 76 77 2. A barcode template is represented as a **Bioplate** item where each coordinate is linked to a **Tag** item. Start by manually creating the required number of bioplates. They should have the following values: 78 79 || **Bioplate type** || !BarcodeTemplate || 80 || **Plate geometry** || 96-well (8x12) || 81 || **Pipeline** (annotation) || MIPs || 55 82 56 83 3. Link the barcodes to templates. This is done by creating (virtual) extracts and link them with tags and positions on one of the bioplates created in the first step. It should be possible to do this with the batch **Extract importer**: … … 61 88 || **Biowell row** || Row coordinate on the template bioplate (A-H) || 62 89 || **Biowell column || Column coordinate on the template bioplate (1-12) || 90 91 92 == 8. User accounts for MIPs pipeline == 93 94 A user account that should work with the MIPs pipeline need to have the following group/role memberships: 95 96 * Groups: `SCAN-B Lab`, `MIPsSecondaryAnalysis` 97 * Roles: `User`, `MIPsLibraryPrep`, `MIPsPlateDesigner` 98