Pre-print available on bioRxiv.
- Information to keep in hand before proceeding:
- MySQL credentials - username, password, database name
- Upscale patterns from the experiment - ie in what combinations were the lower density plates condensed to form the higher density plates
- Name of reference strain being used
- Plate maps of the starting density plate
- One plate per sheet in excel
- Cells contain strain-id
- File should be in .xlsx format
- Example
- Excel table specifying strain-id to orf-name relationships
- First column is strain_id
- Second column is orf_name (should include the reference strain)
- Unique strain-ids for each orf (mutant strain)
- Each strain-id from the platemaps should have an associated orf-name
- File should be in .xlsx format
- Example
- Successful run will create the following tables:
- _borderpos = border positions of all plates in the experiment
- 1 border for 384 density, 2 for 1536 and 4 for 6144
- _pos2coor = position ids and their corresponding plate coordinate
- unique position ids for all possible colony positions in the experiment and thei correspoing plate coordinates ie colony density, plate number, row number and column number
- _pos2orf_name = position ids and the corresponding orf-name (or mutant name)
- _pos2rep = position ids of lowest density plates to their replicates at higher density plates based on the upscale pattern
- for internal use
- _pos2strain_id = position ids and their corresponding strain ids
- _strainid2orf_name = same as excel table from above
- _borderpos = border positions of all plates in the experiment
- Example files can be found in Data.zip.
- Information to keep in handy before proceeding:
- Location of any smudges on the plates ie the colonies you want to remove from the analysis because of any technical issues
- plate number, row number, column number
- Location of any smudges on the plates ie the colonies you want to remove from the analysis because of any technical issues
- User will be asked to verify binary files before uploading raw pixel count data
- Each image will now have 3 additional files - .binary, .cs.txt and .info.mat
- View the .binary file (using Preview in Mac) to verify if the colonies have been correctly identified
- Successful run will create the following tables:
- _RAW = raw colony size estimations per hour per position id of all the images
- image1, image2 and image3 columns correspond to the three images per plate
- average column is the mean of the pixel count estimation from the three images
- image1 = image2 = image3 = average if there is a single image per plate
- _smudgebox = position ids corresponding to the user defined coordinates
- _JPEG = similar to _RAW with
- pixel count estimations for borders and smudgebox NULL'd
- and any pixel count estimation < 10 is also NULL'd - likely to be a light artifact
- _RAW = raw colony size estimations per hour per position id of all the images
- If the images are already analyzed using a different software then make sure the colony sizes in the _JPEG table are arranged in ascending order of hours, plate number, column number, row number.
- Example files can be found in Data.zip.
- Successful run will create the following tables:
- _NORM = position ids and their corresponding relative fitness measurements
- also includes the background pixel count measurement based on references
- _FITNESS = similar to _NORM but with strain ids and orf-names included
- _FITNESS_STAT = strain-id-wise mean, median and standard deviation of relative fitness
- _PVALUE = strain-id-wise empirical p-values
- stat = (strain mean fitness - reference mean fitness)/reference fitness standard deviation
- es = (strain mean fitness - reference mean fitness)reference mean fitness
- _NORM = position ids and their corresponding relative fitness measurements
- Example files can be found in Data.zip.