Abstract: There is provided a method for determining an error in image data of bodily fluid testing equipment. The method comprises detecting (S304) a first colour of a first testing region in the image data, comparing (S306) the detected first colour to reference colours, determining (S308) respective difference scores between the detected first colour and the reference colours, determining (S310) a closest reference colour wherein the closest reference colour has a lowest difference score, determining (S312) whether the difference score between the detected first colour and the closest reference colour is less than a predetermined maximum difference score, performing (S380) a first action when the difference score is less than the predetermined maximum difference score, and determining (S390) that there is an error in the first testing region in the image data and performing a second action when the difference score is not less than the predetermined maximum difference score.

Abstract: A method for determining an indicator of a bodily condition in an image of a bodily fluid testing equipment captured by an electronic device is provided. The method comprises acquiring image data of a bodily fluid testing equipment (100, 200), determining at least one edge (539) of a first bodily fluid testing region (109, 209), determining a location of the first bodily fluid testing region, sampling colour data of a sub-region (541) of the first bodily fluid testing region, determining, based upon the sampled colour data, whether an indicator of a bodily condition has interacted with the first bodily testing region and providing an output, wherein the output is based upon whether the indicator of the bodily condition has interacted with the first bodily fluid testing region.

Abstract: An application-analysable bodily fluid testing equipment (100, 200, 300) is provided. The application-analysable bodily fluid testing equipment comprises at least one testing region (109, 209, 309) sensitive to an indicator of a bodily condition in bodily fluid from which image data is capturable and analysable by an associated application on a device. The bodily fluid testing equipment further comprises a handling indicator (107, 207, 307) indicating an area of the equipment for a user to hold during the application of a bodily fluid to the at least one testing region, and during capture of the image data for analysis of the bodily fluid applied to the at least one testing region using the application on the device.

Abstract: A lateral flow bodily fluid testing system is provided. The system comprises an application-analysable bodily fluid testing equipment (100, 200, 300) and an electronic device (1001) comprising a camera (1002) and one or more processors (1004). The one or more processors are configured to acquire image data of the application-analysable bodily fluid testing equipment with the camera of the electronic device, perform testing of bodily fluid applied to the application-analysable bodily fluid testing equipment using the image data to determine whether indicators of one or more bodily conditions are present in the applied bodily fluid, and output a result indicating whether the indicators of one or more bodily conditions are present in the applied bodily fluid.

Abstract: A method for determining an indicator of a bodily condition in an image of a bodily fluid testing equipment captured by an electronic device is provided. The method comprises determining colour data of a first bodily fluid testing region (109, 209) of a bodily fluid testing equipment (100, 200) from image data of the bodily fluid testing equipment, determining colour calibration data of at least one background sub-region (543) of a background region (545) of the bodily fluid testing equipment, calibrating the colour data based upon the determined colour calibration data, determining whether an indicator of a bodily condition has interacted with the first bodily fluid testing region, and providing an output, wherein the output is based upon whether the indicator of the bodily condition has interacted with the first bodily fluid testing region.

Abstract: There is provided a method for determining an error in image data of bodily fluid testing equipment. The method comprises detecting (S304) a first colour of a first testing region in the image data, comparing (S306) the detected first colour to reference colours, determining (S308) respective difference scores between the detected first colour and the reference colours, determining (S310) a closest reference colour wherein the closest reference colour has a lowest difference score, determining (S312) whether the difference score between the detected first colour and the closest reference colour is less than a predetermined maximum difference score, performing (S380) a first action when the difference score is less than the predetermined maximum difference score, and determining (S390) that there is an error in the first testing region in the image data and performing a second action when the difference score is not less than the predetermined maximum difference score.

Abstract: A method for determining an indicator of a bodily condition in an image of a bodily fluid testing equipment captured by an electronic device is provided. The method comprises acquiring image data of a bodily fluid testing equipment (100, 200), determining at least one edge (539) of a first bodily fluid testing region (109, 209), determining a location of the first bodily fluid testing region, sampling colour data of a sub-region (541) of the first bodily fluid testing region, determining, based upon the sampled colour data, whether an indicator of a bodily condition has interacted with the first bodily testing region and providing an output, wherein the output is based upon whether the indicator of the bodily condition has interacted with the first bodily fluid testing region.

Abstract: A method for determining an indicator of a bodily condition in an image of a bodily fluid testing equipment captured by an electronic device is provided. The method comprises determining colour data of a first bodily fluid testing region (109, 209) of a bodily fluid testing equipment (100, 200) from image data of the bodily fluid testing equipment, determining colour calibration data of at least one background sub-region (543) of a background region (545) of the bodily fluid testing equipment, calibrating the colour data based upon the determined colour calibration data, determining whether an indicator of a bodily condition has interacted with the first bodily fluid testing region, and providing an output, wherein the output is based upon whether the indicator of the bodily condition has interacted with the first bodily fluid testing region.

Abstract: A lateral flow bodily fluid testing system is provided. The system comprises an application-analysable bodily fluid testing equipment (100, 200, 300) and an electronic device (1001) comprising a camera (1002) and one or more processors (1004). The one or more processors are configured to acquire image data of the application-analysable bodily fluid testing equipment with the camera of the electronic device, perform testing of bodily fluid applied to the application-analysable bodily fluid testing equipment using the image data to determine whether indicators of one or more bodily conditions are present in the applied bodily fluid, and output a result indicating whether the indicators of one or more bodily conditions are present in the applied bodily fluid.

Abstract: An application-analysable bodily fluid testing equipment (100, 200, 300) is provided. The application-analysable bodily fluid testing equipment comprises at least one testing region (109, 209, 309) sensitive to an indicator of a bodily condition in bodily fluid from which image data is capturable and analysable by an associated application on a device. The bodily fluid testing equipment further comprises a handling indicator (107, 207, 307) indicating an area of the equipment for a user to hold during the application of a bodily fluid to the at least one testing region, and during capture of the image data for analysis of the bodily fluid applied to the at least one testing region using the application on the device.

Abstract: A stabilized deuteroborane-tetrahydrofuran complex is disclosed. Also disclosed are processes for the preparation of the deuteroborane-tetrahydrofuran complex and methods of storing and transporting the prepared complex. The deuteroborane-tetrahydrofuran complexes exhibit enhanced shelf life and increased self-accelerated decomposition temperatures.

Abstract: Herein described are various systems for the creation of unique audio compositions by first searching collections of purpose-created audio layers and then selecting audio layers that meet the user's criteria. The unique structure and classification of audio layers in the library allows non-musicians a foolproof method to compose harmonious and synchronous original compositions. The user previews versions of the selected layers and mixes the layers to obtain a draft multilayer version of the desired sounds. Once a desired sound is achieved, the user can then download high resolution performance versions the compiled layers or individual selected audio layers to mix and achieve the desired final audio composition.