Abstract: Provided is a direct radiating array (“DRA”) antenna, the antenna including a printed circuit board (“PCB”) having a first side and a second side opposing the first side, a thermal interface plate arranged generally parallel to the PCB, a plurality of radiating elements mounted to the first side of the PCB, a plurality of radio frequency (“RF”) chains mounted to the second side of the PCB and to the thermal interface plate, each respective one of the plurality of RF chains coupled to and located proximate to a respective one of the plurality of patch radiating elements and thermally coupled to the thermal interface plate and a plurality of beamforming circuits mounted to the second side of the PCB, wherein each of the RF chains is connected to at least one of the plurality of beamforming circuits.

Abstract: A computer-implemented method that is for assessing pathogenicity of a variant for a patient. Receive a variant. Determine at least one probability for the variant in relation to pathogenic metrics based on a collection of learned variants. The pathogenic metrics comprise a data representation of at least one genetic condition cluster for determining at least one probability for the variant. The combined representation of at least one probability of the variant for the patient is outputted.

Abstract: A screening system includes control circuitry that determines gene variants present in a compiled genome representative of a subject based on a difference between a reference genome and the compiled genome representative of the subject, and acquires phenotype information from an observation of the subject. The control circuitry further generates multi-dimensional data structure that includes the gene variants in respect of a first dimension, the phenotype information in respect of a second dimension; and a set of data samples in respect of a third dimension. The set of data samples includes the compiled genome sequence representative of the subject, and corresponding historical data samples of other subjects including their corresponding transcript information (for example, including phenotype information) of the other subjects and their gene variants.