Comments (4)
Jeff B wrote (Tuesday, 8 September 2020 at 08:31)
For picking samples the key data will be the Cq values from the first 3 channels (which are the SARS-CoV2 test PCR products). However, it is helpful to know the positive control (channel 4) and the calls they make as part of our ongoing comparisons, so if it is not too difficult for the LIMS team to add those as well, then I think that is safest. Finally, the Target columns are obviously hugely redundant, and so the only reason for keeping them is to be able to track if the lab changes their target, or to compare across labs which may have different targets (indeed, I think Cambridge may only use one?).
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Rich L wrote (Friday, 25 September 2020 at 17:28)
Can you check my understanding below for the CT value features, 1) parsing + persisting data and 2) filtering samples out of positive report
...
Remove sample from pick list when following rule fires
High CT rule: Remove sample when one or more of CH1-Cq, CH2-Cq or CH3-Cq values > 29?
Q. Will CT threshold be the same for all labs?
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Jeff B wrote (Monday, 28 September 2020 at 12:39)
The rule should fire if all non-missing channels are > 30. (CH1-Cq > 30 && CH2-Cq > 30 && CH3-Cq > 30)
Threshold will be same for all labs, though if one lab provides fewer than three channels, it applies to as many as there are.
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To test this and related stories (#126, #129):
In UAT:
- Make sure have deployed Andrew's stories (sanger/crawler#108 etc.)
- Wait until some samples are imported by nightly crawler that have Ct values, or create some dummy samples in the MongoDB - we want a mix of:
- positive samples with no Ct value data
- positive samples with Ct values > 30
- positive samples with Ct values < 30
- positive samples with mixed Ct values
- positive samples where Root Sample ID starts with 'CBIQA_'
- Run the Lighthouse 'positives on site report' & check that some samples are filtered out based on correct criteria
- Scan plate barcodes of some of above samples into UAT LabWhere
- Run Lighthouse Sentinel Sample Creation and check samples are imported based on same correct criteria
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Related Issues (20)
- DPL-470 - LSPA date tested in future HOT 1
- DPL-472 - Brants Bridge sent root sample ids in incorrect format
- DPL-473 - Brants Bridge sent ~1500 samples with incorrect RNA ID HOT 1
- DPL-342 Remove report [C=S, V=3]
- DPL-362 As GSU (Alan K) I want to allocate a unique COG-UK ID to all historic Heron samples so that we can use this instead of Root Sample ID within our internal tracking. HOT 10
- DPL-426 Remove updates for MLWH once all samples arrive via RabbitMQ HOT 2
- DPL-429 As developer I want to remove the lighthouse reports generation as is not in use anymore and want to have less code to maintain HOT 1
- DPL-544 Make data consistent between MongoDB, MLWH and Sequencescape
- DPL-614 Missing plate map (Heron)
- DPL-631 [BUG] Incorrect evaluation of must_sequence affects both Box buster and Biosero HOT 1
- DPL-629 Check status of Heron CP plates HOT 1
- DPL-675-2: AROUND SEPTEMBER 2023 -- Remove reports and Sentinel functionality HOT 1
- DPL-717-1: Create a new endpoint for creating entities for Lighthouse deep-well plates in Sequencescape
- DPL-757 As PSD I want to create a first draft design for RVI new project (multipick) that will reflect lims architecture and required components to solve the current list of user requirements obtained.(S=M; C=L) HOT 1
- DPL-776 Investigate a way to identify Heron/RVI samples already in SequenceScape so that we can avoid problems during stamping from deep wells to shallow well plates for RVI.
- DPL-782 Filter samples being imported for deep-well to shallow-well stamping so as to exclude samples already in Sequencescape
- DPL-821 [RVI] Cherry-picking LSW-96 Stock plates using the existing Tecan systems HOT 4
- DPL-670-4 Pass a Lighthouse specific API key to Sequencescape calls HOT 3
- DPL-840 Populate missing sample fields in MLWH and consequently in CoTrack
- Y24-191 - Use the v2 API key for all Sequencescape requests
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