Abstract: A device for determining a HRD index of presence of Homologous Recombination Deficiency, HRD, in a genome of a subject, the device being configured for: receiving shallow WGS data and non-shallow sequencing data relative to a group of genes in the subject genome, obtaining at least one first parameter from the shallow WGS data and at least one second parameter from non-shallow sequencing data, and determining, by applying a HRD prediction Machine Learning Model to the obtained at least first and second parameters, an HRD index representative of presence of HRD in the subject genome.

Abstract: A computer-implemented method for decision support of a user to standardize phenotyping in genomic analysis of a subject, wherein the method includes: receiving a list of symptoms having at least one symptom observed for the subject; receiving a first graph having nodes and weighted links; receiving a second graph being previously obtained applying a matrix factorization to a gene-symptom matrix; and outputting at least one gene associated to the list of symptoms based on the first graph and on the second graph.

Abstract: A genomic data analysis architecture includes a plurality of application nodes, each application node including a calculation system including at least one calculation node, the calculation system being constructed and arranged so as to carry out genomic calculations, a human-machine interface constructed and arranged so as to communicate with the calculation system, and a knowledge base access interface, and including a knowledge base constructed and arranged so as to communicate with the plurality of application nodes. The knowledge base contains genomic data.

Abstract: Elevator component access cabinets are provided. The elevator component access cabinets include a housing having an access door, a sliding element contained within the housing, and at least one elevator component pivotably mounted to the sliding element about a first pivot. The sliding element is movable between a first state and a second state, and wherein when in the first state, the at least one elevator component is stowed within the housing and in the second state the at least one elevator component is located outside of the housing, and the at least one elevator component is pivotable about the first pivot to enable access to the at least one elevator component.

Abstract: A genomic data analysis architecture includes a plurality of application nodes, each application node including a calculation system including at least one calculation node, the calculation system being constructed and arranged so as to carry out genomic calculations, a human-machine interface constructed and arranged so as to communicate with the calculation system, and a knowledge base access interface, and including a knowledge base constructed and arranged so as to communicate with the plurality of application nodes. The knowledge base contains genomic data.

Abstract: The invention relates to providing access to data of a digital book on a remote server (SER), wherein, in particular, at least one URL address is provided, said URL address pointing to the data of a single digital book. To this end: a) a hardware medium (CA) is provided, said hardware medium comprising a hidden indicator (COD) for a hardware-medium identifier, as well as an indicator for a first portion (URL1) of said URL address; and b) the server correlates the hardware-medium identifier with said data of the single digital book, in order to make the data of said single digital book accessible at a URL address created by the concatenation of said first URL address portion and the hardware-medium identifier.