Abstract: The present invention relates to a method of providing information for predicting cancer recurrence and prognosis using a patient-specific panel. According to the method for predicting cancer recurrence according to one embodiment of the present invention, it is possible to predict cancer recurrence and prognosis with increased sensitivity and accuracy.

Abstract: The present invention relates to a method for preparing a multi-analytical prediction model for cancer diagnosis and a method of providing information for cancer diagnosis using the same. The method of preparing a multi-analytical prediction model for cancer diagnosis according to one embodiment of the present invention and the method of providing information for cancer diagnosis using the prediction model have advantages in that it is possible to diagnose cancer with high accuracy and sensitivity and to diagnose cancer at an early stage.

Abstract: The present invention relates to a method of identifying false positive variants during nucleic acid sequencing. According to one embodiment of the present invention, it is possible to effectively identify and remove false positive variants using the context error rate of HQS obtained from an amplified nucleic acid fragment.

Abstract: A method and a system thereof for generating a personalized biological age prediction model are proposed. The method and the system generate a model capable of predicting a biological age for each individual by obtaining an excess age for a chronological age for each age on the basis of medical checkup data. More particularly, the method and the system build a biological age prediction model by gender and chronological age group in consideration of aging mechanisms different from each other according to the gender and the chronological age group, and enable predicting the biological age according to the biological age prediction model for each age group.

Abstract: The present invention relates to a DNA methylation marker for predicting the recurrence of liver cancer by using the difference in the DNA methylation levels according to a liver cancer prognosis, and when the marker is used, the recurrence of liver cancer can be easily predicted, and a more personalized treatment for patients at high risk of liver cancer recurrence can be provided and clinical information for avoiding unnecessary over-treatment can be provided.

Abstract: The present invention relates to a method for assessing the prognosis or risk stratification of liver cancer by using a clinical specimen mixed with a normal tissue, wherein at least one CpG site that shows a low methylation level in normal and blood tissues but a high methylation level in only a cancer tissue is measured for methylation level.

Abstract: The present disclosure relates to a statistical analysis system. More particularly, the present disclosure relates to a statistical analysis system capable of inferring the purpose of a user's analysis, etc. through questions and answers with the user so that ordinary people easily acquire clinical and statistical analysis information, the system using a conversational interface adapted to a statistical analysis for clinical data.

Abstract: The present invention relates to a method for assessing the prognosis or risk stratification of liver cancer by using a clinical specimen mixed with a normal tissue, wherein at least one CpG site that shows a low methylation level in normal and blood tissues but a high methylation level in only a cancer tissue is measured for methylation level.

Abstract: Provided are a method and an apparatus for preparing medicines. The method for preparing medicines includes a distribution step of distributing at least one pill into at least one medicine packet and a crushing step of applying a pressure to the medicine packet with the pill to crush the pill. The apparatus for preparing medicines includes a distributor configured to distribute at least one pill into at least one medicine packet and a crusher configured to apply a pressure to the medicine packet with the pill to crush the pill.

Abstract: Provided are a method and an apparatus for preparing medicines. The method for preparing medicines includes a distribution step of distributing at least one pill into at least one medicine packet and a crushing step of applying a pressure to the medicine packet with the pill to crush the pill. The apparatus for preparing medicines includes a distributor configured to distribute at least one pill into at least one medicine packet and a crusher configured to apply a pressure to the medicine packet with the pill to crush the pill.

Abstract: A sanitary finger cap including: an insertion portion having a generally cylindrical shape and adapted to be fitted to a third knuckle of a finger connected to the center of a hand or to a portion of a second knuckle of the finger; and a grasping portion connected with one side of the insertion portion as a unitary body, in a shape of a general corn or pyramid in such a manner as to become small in thickness as it goes toward the other side thereof, and adapted to be fitted to a first knuckle as the end portion of the finger or to the second knuckle of the finger so as to grasp food thereon.

Abstract: A packaging container heated together with contents accommodated inside therein according to the present invention includes: a first cover part having a packaging area and a sealing area surrounding the packaging area; and a second cover part facing the first cover part and coupled to the first cover part in the sealing area. Further, each of the first cover part and the second cover part includes: a base layer, a first auxiliary layer formed on the base layer, and a second auxiliary layer formed on the base layer so as face the first auxiliary layer with the base layer interposed therebetween. The base layer is implemented by a Casted Polypropylene (CPP) film, the first auxiliary layer is implemented by the CPP film including Epoxidised Butadiene Rubber (EBR), and the second auxiliary layer includes the same material as that of the first auxiliary layer.

Abstract: A packaging pouch according to the present invention includes a first cover part, a second cover part, and coupling parts. The first cover part includes a packaging area and a sealing area surrounding the packaging area, and a second cover part faces the first cover part to be coupled to the first cover part in the sealing area. Further, the coupling parts are arranged while being spaced apart from each other on the first cover part and the second cover part in the packaging area, and couple the first cover part and the second cover part to each other.

Abstract: The present invention relates to a sanitary finger cap including: an insertion portion having a generally cylindrical shape and adapted to be fitted to a third knuckle of a finger connected to the center of a hand or to a portion of a second knuckle of the finger; and a grasping portion connected with one side of the insertion portion as a unitary body, in a shape of a general corn or pyramid in such a manner as to become small in thickness as it goes toward the other side thereof, and adapted to be fitted to a first knuckle as the end portion of the finger or to the second knuckle of the finger so as to grasp food thereon.

Abstract: Light-generating fusion proteins having a ligand binding site and a light-generating polypeptide moiety and their use as diagnostics, in drug screening and discovery, and as therapeutics, are disclosed. The light-generating fusion protein has a feature where the bioluminescence of the polypeptide moiety changes upon binding of a ligand at the ligand binding site. The ligand may be, for example, an enzyme present in an environment only under certain conditions, e.g., ubiquitin ligase in a hypoxic state, such that the light-generating fusion protein is “turned on” only under such conditions.

Abstract: An apparatus and method for driving an LCD device is provided. The apparatus for driving an LCD device comprises an image display unit that includes liquid crystal cells formed in each region defined by a plurality of gate lines and a plurality of data lines. A data driver supplies analog video signals to the respective data lines. A gate driver supplies scan pulses to the respective gate lines. A data converter detects motion vectors from input data and generating modulated data by filtering the input data in accordance with the motion vectors to generate overshoot or undershoot in a boundary along a motion direction. A timing controller aligns the modulated data to supply the aligned data to the data driver and operates the data driver and the gate driver.

Abstract: Light-generating fusion proteins having a ligand binding site and a light-generating polypeptide moiety and their use as diagnostics, in drug screening and discovery, and as therapeutics, are disclosed. The light-generating fusion protein has a feature where the bioluminescence of the polypeptide moiety changes upon binding of a ligand at the ligand binding site. The ligand may be, for example, an enzyme present in an environment only under certain conditions, e.g., ubiquitin ligase in a hypoxic state, such that the light-generating fusion protein is “turned on” only under such conditions.

Abstract: A liquid crystal display device according to an embodiment of the present invention includes at least two liquid crystal display panels; a lamp to irradiate light on each of the liquid crystal display panels; a transparent case to cover the lamp; and a hinge part to provide a hinge function to each of the liquid crystal display panels.

Abstract: The liquid crystal display device includes a histogram analyzer analyzing a histogram of an input image and determining the input image as being in one of a low brightness mode, a normal mode, and a high brightness mode based on the histogram analysis, a back light controller controlling a maximum brightness of a back light unit based on the mode determination, and a data modulator enlarging the histogram of the input image to modulate data of the input image. The histogram analyzer detects a most frequent value of gray scale occurring most frequently in the input image of one frame, compares the most frequent value with a predetermined low reference gray value and a predetermined high reference gray value, and determines the input image as in one of the low brightness mode, the normal mode, and the high brightness mode based on the compared result.

Abstract: A resistive type touch panel includes a first substrate aligned to be facing a second substrate. The first substrate includes a first conductive layer and the second substrate includes a second conductive layer. A plurality of spacers each having a polygonal column shape are disposed between the first and second substrates in predetermined positions. The geometry and center-to-center spacing of the spacers minimizes detection of a distributed activation force applied to one of the first and second substrate while still providing sensitivity to detect concentrated application of an activation force to one of the first and second substrates.