using the master version of gems
bumped the version to 1.12.2
Merge pull request #104 from ke4/merge_68426346_concentrations_issue_in_sequencescape

Merge 68426346 concentrations issue in sequencescape
bumped version to 1.12.3
using the latest lims applications

(lims-core/laboratory/management/quality)
Merge pull request #106 from ke4/merge_68549708_biorobot_plates_not_supported_in_sscape

Merge 68549708 biorobot plates not supported in sscape
[#68885972] Update the aliquots in supported plates
bumped version to 1.12.4
Merge pull request #107 from ke4/68885972_in_sscape_the_plates_and_samples_are_not_joined

68885972 in sscape the plates and samples are not joined
[#68885972] The asset links and transfer requests

only created for supported plates
bumped the version to 1.12.5
Merge pull request #108 from ke4/68885972_in_sscape_the_plates_and_samples_are_not_joined

68885972 in sscape the plates and samples are not joined
[#69086840] added new action to routing keys
[#69086840] added decoder for BulkCopySample
bump version to 1.12.6
Merge pull request #109 from ke4/69086840_add_BulkCopySample_action

69086840 add bulk copy sample action
bumped version to 1.12.7
using the latest management-app (3.3.0)
Merge pull request #110 from ke4/using_management_330

Using management 330
RNA working silution plates use different purpose

Fluidigm submissions in Sequencescape are made from working dilution
plates. These are selected using a purpose and a sample name. However
if a sample has come across the bridge, but DNA and RNA samples are
on Working Dilution plates, and Sequencescape can't distinguish between
them. (Except by barcode prefix, but using that would break pattern)

I've added a new purpose to Sequencescape for RNA Working Diltion.
I believe these changes are all thats needed to ensure the bridge uses it,
but as I'm not familiar with the inner workings of S2 or the bridge,
I may have missed something important.