new clinical trial xna extraction worksheets - adapted existing molecular xna extraction worksheet functions to handle both molecular & clinical trial sections; had to use fully qualified method name for weaken() in RecordHandler or mail_reports & diagnosis_status_alerts crons fail with fatal error; substituted leedsth.nhs.uk in 'from' address and added 'reply-to' header to emails to suppress nhs.net appended warnings; temporarily suspended Family ID requirement for Rare disease SLF; grouped common barcode styles
replaced MAX(CASE WHEN ..) in genomics_sample_linkage_form_data query - doesn't work with n = 1; replaced 2 inactive lab_test_result_options for inactive fixation menu
added request.id & patient_case.id to registration_search to override precedence given by RDBO; updated xml generation & validation with changes for cancer dataset - should still work for rare diseases
sort order for LabTestResultDataType objects; genomics_sample_linkage_form_data doesn't need left join for request_lab_test_results as family_id is required field in dependent query; fix for results.t after putting html_line_break on result summaries; for clarity changed wording of 'amended report issued by' on report
genomics sample linkage form; xsd validation for genomics_xml.pl; bugfix for audit/turnaround_percentile.tt - subtraction only performed if values exist
adapted allow >1 central laboratory (Genomics); new cfg flag to allow all requests to be reporter-authorised (UCLH); bugfix to user_permission.tt display; tweaked genomics_xml.t after changing consent taken to consent given
bugfix - panels.tt required match regex on auto_expand; moved genomics_unit_number query closer to genomics_demographics to avoid ge/le mistake in date_sub when testing