Changes between Initial Version and Version 1 of LEGACY - CaTissue Automatic specimen Labelling


Ignore:
Timestamp:
03/08/13 11:21:20 (12 years ago)
Author:
Nick Holden
Comment:

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  • LEGACY - CaTissue Automatic specimen Labelling

    v1 v1  
     1CaTissue has a facility for automatic labelling (and barcoding) of specimens. We have had this turned off because we don't want CaTissue to generate barcodes, as the aliquot storage tubes are all barcoded on manufacture. However, it turns out we can have auto labelling, without auto barcodes. This would speed up data entry for projects (other than BRICCS, because of the API client doing this automatically anyway).
     2
     3So... we need to test our existing labelling scheme for compliance with the token system available in CaTissue.
     4
     5Using the DEV deployment...
     6
     71. GENVASC
     8
     9* Primary samples:
     10
     11  * prefix "s" for the whole blood which generates the serum sample (collected in serum separator vacutainer)
     12  * prefix "e" for the whole blood which generates the plasma sample (collected in edta vacutainer)
     13  * Collection Protocol ID (e.g. "G00007")
     14
     15  * Thus: "sG00007" and "eG00007"
     16
     17* Derived samples
     18
     19  * Primary sample label
     20  * Alphabetical ordinal ("a", "b", "c", etc)
     21
     22  * Thus: "sG00007a", "eG00007a" and "eG00007b"
     23
     24* Aliquots
     25
     26  * Manually entered 2D barcodes.
     27
     28
     29Problems:
     30  1. The token system available doesn't differentiate by container, only by specimen type.
     31  2. Ordinals are only available as numbers, not letters.
     32  3. DNA is derived - just check what happens, will the DNA be auto-labelled? That would probably be OK.
     33
     342. BIOSTAT
     35
     36No auto-labelling required - all specimen arrive in 2d barcode tubes.
     37
     383. Prestige
     39
     40* Only one primary sample:
     41
     42  * Collection Protocol ID
     43
     44* Derived samples
     45
     46  * Primary sample label
     47  * Suffix of "-" followed by the sample type abbreviation, using P for plasma and B for Buffy coat.
     48
     49* Aliquots
     50
     51  * Manually entered 2D barcodes.
     52
     53Problems:
     54  1. Derived samples use different abbreviations to the BRICCS and GENVASC protocols, and abbreviations.xml is a site-wide configuration file.
     55  2. The abbreviations a bit odd - "B" for Buffy Coat, and P for "edta plasma". But it is the only plasma in this CP.
     56
     574. DREAM
     58
     59* Primary samples (two visits, two samples per visit)
     60
     61  * Collection Protocol ID
     62  * Alphabetical ordinal ("a", "b", "c", etc)
     63
     64* Derived samples
     65
     66  * IT SHOULD BE: Parent specimen ID with a suffix for specimen type ("p" for plasma and "s" for serum).
     67  * But there's a problem. The first visit specimens are being labelled with the CP ID and the suffix, which means the second visit specimen will have the same labels.
     68
     69Problems:
     70  1. Ordinals are only available as numbers, not letters.
     71  2. The labelling scheme for the derived samples needs fixing.
     72
     73
     745. MVO
     75
     76* Primary samples
     77
     78  * Collection Protocol ID
     79  * Suffix of "-" followed by an ordinal relating to the visit event
     80
     81Problems
     82  1. Ordinal based on visit event isn't currently possible. If third visit is missed, next sample should be "4" but would get a "3". Could we add a token to include the
     83
     846. BRICCS-HDL - not yet recruited. Real soon now.
     85
     86* Primary sample (additional EDTA): BSa number as the specimen is obtained during BRICCS recruitment
     87
     88* Derived sample: prefix "e" for edta plasma, followed by the Collection Protocol ID.
     89