Abstract: Disclosed in the present invention is a method for decoding Chinese character writing for an invasive brain-computer interface. In a practical application, a corresponding motor neural signal is divided into two states of a writing stroke and a writing stroke break in view of inconsistency of the writing stroke and the writing stroke break during Chinese character writing, and different filters are trained. A hidden markov model (HMM algorithm) and a Viterbi algorithm are used to judge a task state of the motor neural signal, and the corresponding signal is put into a corresponding decoder. The present invention effectively reduces influence of difference of neural data in different states on the decoder, and improves the performance and robustness of the decoder.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: A thermally activated delayed fluorescent material and an electroluminescent device. The thermally activated delayed fluorescent material has a structure as shown in the following formula.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: A display substrate and a display device are provided. The display substrate includes: a base substrate; and a light-emitting element arranged on the base substrate, and including a first electrode, an organic functional layer and a second electrode arranged sequentially in that order in a direction away from the base substrate. The light-emitting element includes a first surface proximate to the base substrate, a second surface distal to the base substrate, and a side surface arranged between the first surface and the second surface. The display substrate further includes a reflection layer covering at least a part of the side surface and configured to reflect light from the organic functional layer.

Abstract: A system and method of uniform sampling in an append-only database to determine temporal distribution of data.

Abstract: A display substrate and a display device are provided. The display substrate includes: a base substrate; and a light-emitting element arranged on the base substrate, and including a first electrode, an organic functional layer and a second electrode arranged sequentially in that order in a direction away from the base substrate. The light-emitting element includes a first surface proximate to the base substrate, a second surface distal to the base substrate, and a side surface arranged between the first surface and the second surface. The display substrate further includes a reflection layer covering at least a part of the side surface and configured to reflect light from the organic functional layer.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: A display substrate and a display device are provided. The display substrate includes: a base substrate; and a light-emitting element arranged on the base substrate, and including a first electrode, an organic functional layer and a second electrode arranged sequentially in that order in a direction away from the base substrate. The light-emitting element includes a first surface proximate to the base substrate, a second surface distal to the base substrate, and a side surface arranged between the first surface and the second surface. The display substrate further includes a reflection layer covering at least a part of the side surface and configured to reflect light from the organic functional layer.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: A structure for sealing a button-type lithium cell includes a cell cover, a sealing ring and a cell casing. The cell cover includes an overlapping structure. The overlapping structure includes a first overlapping portion, a second overlapping portion and a third overlapping portion and the third overlapping portion includes a locking portion and a sealing portion. The cell casing includes a sealing structure. The sealing structure includes a first sealing portion, a second sealing portion, a third sealing portion and a fourth sealing portion. The first overlapping portion abuts against the fourth sealing portion through the sealing ring, the second overlapping portion abuts against the third sealing edge through the sealing ring, the locking portion of the third overlapping portion abuts against the second sealing edge through the sealing ring, and the sealing portion of the third overlapping portion abuts against the first sealing edge through the sealing ring.

Abstract: A structure for sealing a button-type lithium cell includes a cell cover, a sealing ring and a cell casing. The cell cover includes an overlapping structure. The overlapping structure includes a first overlapping portion, a second overlapping portion and a third overlapping portion and the third overlapping portion includes a locking portion and a sealing portion. The cell casing includes a sealing structure. The sealing structure includes a first sealing portion, a second sealing portion, a third sealing portion and a fourth sealing portion. The first overlapping portion abuts against the fourth sealing portion through the sealing ring, the second overlapping portion abuts against the third sealing edge through the sealing ring, the locking portion of the third overlapping portion abuts against the second sealing edge through the sealing ring, and the sealing portion of the third overlapping portion abuts against the first sealing edge through the sealing ring.

Abstract: Immune context scores are calculated for tumor tissue samples using continuous scoring functions. Feature metrics for at least one immune cell marker are calculated for a region or regions of interest, the feature metrics including at least a quantitative measure of human CD3 or total lymphocyte counts. A continuous scoring function is then applied to a feature vector including the feature metric and at least one additional metric related to an immunological biomarker, the output of which is an immune context score. The immune context score may then be plotted as a function of a diagnostic or treatment metric, such as a prognostic metric (e.g. overall survival, disease-specific survival, progression-free survival) or a predictive metric (e.g. likelihood of response to a particular treatment course). The immune context score may then be incorporated into diagnostic and/or treatment decisions.

Abstract: A system and method of uniform sampling in an append-only database to determine temporal distribution of data.

Abstract: A storage controller coupled to a storage array comprising one or more storage devices performs a uniform sampling of data storage items in an append-only file system to identify a sample set and identifies at least two data storage item groups based on an age of the data storage items. The storage controller performs a garbage collection process on the append-only file system to identify stale data storage items in a first logical storage segment and active data storage items in the first logical storage segment and writes a first active data storage item associated with a first group of the two data storage item groups from the first logical storage segment to a second logical storage segment, the second logic storage segment comprising other active data storage items associated with the first group.