GUI Manual
The tool has a tab for each data type (tabular, DICOM) and the usage of the GUI is a straightforward procedure.
First we have to load the dataset csv file.
If we need to validate the data, we need to have a json file containing the table schema (metadata) of the dataset csv file. This json must may follows either a modified frictionless data table-schema specifications or MIP's Data-Catalogue specification schema.
About frictionless schema, the modified schema of that json file can be found here. In short, it is a simple modification that adds MIPType property in the field json object. The acceptable values for this property are text, numerical, integer, nominal and date, depending on the original field object type property value.
Also, in the case where the dataset belongs to a certain MIP's pathology, there is the option to download the dataset's CDE schema from MIP Data Catalogue. The user may save the schema file in a local drive as a json file.
For the report, there are two options file formats:
- excel (xlsx)
For more details about the content of the above files, please refer to the Report Files Descriptions and Details wiki section.
outlier threshold input field is related with the outlier detection for numerical variables of the incoming dataset. The way that the Data Quality Control tool handles the outlier detection of a certain numerical variable, is that first calculates the mean and the standard deviation based on the valid values of that column and then calculates the upper and the lower limit by the formula: upper_limit = mean + outlier threshold * standard deviation, lower_limit = mean - outlier threshold * standard deviation. If any value is outside those limits then it is considered as an outlier.
The report file will be saved in the given output folder, by clicking Create Report button. The name of the output file will be:
-
<dataset>_report.pdf
After reviewing the Cleaning Suggestions either by clicking the button Show cleaning suggestions or by referring the Suggested corrections section in the Data Validation report created in the previous step (Please refer to the Report Files Descriptions and Details wiki section for further details), we can proceed with the data cleaning operation by clicking the Perform Cleaning button. The cleaned dataset file will be saved in the report folder using the original dataset name with the addition of the suffix '_corrected'.
For further details about the validating and cleaning procedure of the DQC tool please refer to the Validation & Cleaning functionality per datatype wiki section.
In this tab we can infer a dataset's schema and save it to the local disk. The schema could be saved in two formats:
- Frictionless spec json
- Data Catalogue's spec Excel (xlsx) file, that can be used for creating a new CDE pathology version.
In the infer option section, we give the number of rows that the tool will based on for the schema inference. Also, we declare the maximum number of categories that a nominal MIPType variable can have.
If we choose the Data Catalogue's excel as an output, the tool offers the option of suggesting CDE variables for each column of the incoming dataset. This option is possible, only when a CDE dictionary is provided. This dictionary is an excel file that contains information for all the CDE variables that are included or will be included in the MIP (this dictionary will be available in the Data Catalogue in the near future). The tool calculates a similarity measure for each column based on the column name similarity (80%) and the value range similarity (20%). The similarity measure takes values between 0 and 1. In the field similarity threshold we can define the minimum similarity measure between an incoming column and a CDE variable that need to be met in order the tool to suggest that CDE variable as a possible correspondence. The tool stores those CDE suggestions in the excel file in the column named CDE and also stores the corresponding concept path under the column conceptPath.
We select the Dicom Root Folder where all the DICOM are stored. It is assumed that for each patient there is a subfolder containing all the MRI dcm files, note that a patient could have more than one MRI. Then, we select the the Output Report Folder where the report files will be placed. If the folder does not exist, the tool will create it. Then, we press the Create Report button.
The tool creates in the <report folder>, the pdf report file dicom_report.pdf and, depending of the results, also creates the following csv files :
- validsequences.csv
- invalidsequences.csv
- invaliddicoms.csv
- notprocessed.csv
- mri_visits.csv
The above files are created even if no valid/invalid sequences/dicoms files have been found. In such case, the files will be empty. Detailed description for the content of these files can be found on the Report Files - Description and Details wiki section.
If we want to filter out the invalid MRI sequences and reorganize the dcm files of the valid MRIs in a suitable folder structure for importing them into LORIS-for-MIP, repeat the previous step and select the Reorganize files for Loris pipeline check button.
For the LORIS pipeline the dcm files are reorganized and stored in a folder structure <ouput_report_folder>/<patientid>/<patientid_visitcount>.
All the dcm sequence files that belong to the same scanning session (visit) are stored in the common folder <patientid_visitcount>.