Changes between Version 1 and Version 2 of Ticket #801, comment 66


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Timestamp:
Oct 30, 2015, 9:30:40 AM (9 years ago)
Author:
olle

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  • Ticket #801, comment 66

    v1 v2  
    99 3. FPA aliquots are placed in consecutive wells, without gaps, downwards in a column, continuing with the first row in the next column to the right, when the last row of a column is reached. Note that this still allows the start well to be on another row, than the first.
    1010 4. DNA aliquots are placed in wells according the scheme above, in the same order, as presented in the wizard lists, i.e. MeLuDI samples before external material, alphabetically listed after name in each group.
    11  5. FPA aliquots are always placed in a column in a way, that at least one well is on the first or last row, i.e. the selected wells always connect with the top or bottom of the plate. Isolated "islands" of selected cells in the middle of a column are not allowed.
     11 5. FPA aliquots are always placed in a column in a way, that at least one well is on the first or last row, i.e. the selected wells always connect with the top or bottom of the plate. Isolated "islands" of selected cells in the middle of a column are not allowed. When starting to fill wells in a column, with all wells available, the column is always filled top to bottom, i.e. the first filled well in the column is on the first row.
     12
     13Requirement 5 has the added implication, that isolated islands of unused wells in a column, where the former do not contain wells on the first or last row, will never be eligible for hosting FPA aliquots. The effective number of wells available for FPA aliquots may therefore be smaller than the number of unused wells.