{"text_format":"1","workbook":"xlsx","n_sheets":2,"sheets":["Sample_Details","Sheet1"],"not_rendered":{"charts":0,"images":0,"macros":1,"external_links":0,"defined_names":32,"comments":0,"pivot_tables":0},"unopened":[],"bounds":{"document_bytes":16777216,"sheet_cells":100000,"rows_first":2000,"rows_last":500,"rows_between":2000,"halvings":0,"cell_chars":16384,"cell_head_chars":4096},"cells_cut":0,"cells_raw":0,"read":"whole","date_system":"1900"}

{"sheet":"Sample_Details","index":0,"n_rows":55,"n_cols":13,"rows_kept":55,"cut":false,"hidden":false,"merged":[[36,3,36,5],[56,0,66,12],[22,3,22,5],[24,3,24,5],[26,3,26,5],[32,3,32,5],[34,3,34,5],[22,10,22,11],[24,10,24,11],[26,10,26,11],[34,10,34,11],[36,10,36,11]]}
["Sequencing and Microarray Facility - 6767 Bertner Ave. Basic Sciences Research Building Room S15.8425   Ph: 713-834-6199"]
["Bio-Rad Droplet Digital PCR Service"]
["Plate Layout Sheet"]
[]
["Instructions for filling out Plate Layout sheet:"]
[]
["All samples should be accompanied by a printed and signed version of the completed Service Request From. The SMF is located in BSRB Room S15.8425"]
["Users must schedule an appointment to drop off reaction plates."]
["1. Sample name entries should be ALPHA-NUMERIC with no spaces."]
["2. Provide 22-25 ul reaction volume per well"]
["3. From the drop-down menu, select the assay type. All samples in one project should be of the same assay. Different assay should be submitted as separate projects."]
["4. Select the supermix from the drop-down menu. If samples require different supermix, please submit them as separate projects."]
["5. All information in \"Section A - Experiment Details\" is required and must be filled in."]
["6. Use \"Section B - Plate Editor\" to define the plate layout. "]
[null,"a. Enter Sample Name"]
[null,"b. Define Target 1 (FAM channel) and select Target 1 Type (from drop down menu)"]
[null,"c. Define Target 2 (VIC or HEX channel) and select Target 2 Type (from drop down menu)"]
[null,"d. Select wells. To select multiple wells, hold Ctrl and select the wells. To select wells in a continuois series (horizontal or vertical), hold Shift and select the first and last wells."]
[null,"e. Click Apply. The settings appear in the well in the plate map."]
[]
["Section A - Experiment Details"]
[]
["ddPCR Experiment / Assay Type:",null,null,null,null,null,null,"Amount of DNA/RNA per reaction (ng):"]
[]
["Supermix:",null,null,null,null,null,null,"Restriction Enzyme Digestion?"]
[]
["Annealing Temperature (°C):",null,null,null,null,null,null,"Restriction Enzyme Used:"]
[]
[]
[]
["Section B - Plate Editor"]
[]
["Sample Name:"]
[]
[" Target 1 (FAM channel):",null,null,null,null,null,null,"Target 1 Type:"]
[]
["Target 2 (VIC or HEX channel):",null,null,null,null,null,null,"Target 2 Type:"]
[]
[]
[]
[]
[]
[]
["Well",1,2,3,4,5,6,7,8,9,10,11,12]
["A"]
["B"]
["C"]
["D"]
["E"]
["F"]
["G"]
["H"]
[]
[]
["Comments:"]

{"sheet":"Sheet1","index":1,"n_rows":6,"n_cols":11,"rows_kept":6,"cut":false,"hidden":false,"merged":[]}
["Absolute Quantification (ABS)",null,null,null,"ddPCR Supermix for Probes (no dUTP)",null,null,null,"Unknown",null,"Yes"]
["Rare Target Sequence Detection (RED)",null,null,null,"ddPCR Supermix for Probes",null,null,null,"Reference",null,"No"]
["Copy Number Variation - Haploid (CNV1)",null,null,null,"Droplet PCR Supermix",null,null,null,"Postivie"]
["Copy Number Variation - Diploid (CNV2)",null,null,null,"One-Step RT PCR kit for Probes",null,null,null,"Negative"]
["Gene Expression (GEX)",null,null,null,"QX200 ddPCR EvaGreen Supermix",null,null,null,"Blank"]
[null,null,null,null,null,null,null,null,"NTC"]