A method and system for pooling a plurality of specimens for processing, each specimen associated with a set of specimen characteristics. Each specimen is grouped based on the set of specimen characteristics, where the set of specimen characteristics includes a mass of each specimen. A set of flow cell characteristics for each flow cell included in a group of flow cells that includes at least one flow cell is identified. At least one pool is generated based on the set of specimen characteristics associated with each specimen included in the plurality of specimens and the set of flow cell characteristics for each flow cell included in the group of flow cells. Each pool is associated with a lane included in a flow cell and includes at least one specimen included in the plurality of specimens, and each lane is associated with a specimen type.

An automatic measurement system for Sludge settling Velocity comprises a sampling and shooting module, a data service module, data processing module, and a measurement and analysis module. The sampling and shooting module is configured to collect samples and to obtain a test images of samples. The data processing module is configured to collect and store process data. The measurement and analysis module is configured to obtain the sedimentation ratios of samples according to test images. The sludge activity is analyzed according to the sedimentation ratios. When the sludge activity is abnormal, the process data are obtained from data processing module, and the process analysis data are obtained according to the data and the sludge activity analysis results. The automatic measurement system can avoid errors caused by manual measurement and improve accuracy and efficiency of detection and can avoid the problems of untimely detection.

Disclosed are a dilution method and a dilution apparatus. The dilution method includes: adding a sample into a first reactor at a first station of a supply unit; transferring the first reactor to a fifth station of a transit apparatus, and receiving a second reactor at the first station of the supply unit; adding a diluent into the first reactor at the fifth station to obtain a diluted sample; uniformly mixing the diluted sample in the first reactor; transferring the first reactor from the transit apparatus to a dilution transport apparatus; transferring part of the diluted sample in the first reactor to the second reactor; transferring the second reactor to the fifth station of the transit apparatus, and continuing to add the diluent into the second reactor; and uniformly mixing substances in the second reactor. The dilution apparatus includes the supply unit and the transit apparatus.

A method to provide control samples for validating a diagnostic test within a laboratory system is presented. The laboratory system comprises an aliquoting device, a storage, a transport system, at least two analyzers, and a control unit. A total number of control sample aliquots and an aliquot volume for each control sample aliquot is determined based on a validation time schedule. A provided total control sample volume is aliquoted into the determined total number of control sample aliquots with the determined aliquot volumes. The generated control sample aliquots are transported to one or more of the at least two analyzers according to the validation time schedule.

An automated laboratory system for processing biological samples in a batch type manner is disclosed. In one embodiment, the system may receive assay instructions for biological samples processing among a plurality of devices. The devices may include a pre-analytical instrument and one or more analysis systems. The system may include an orchestration core application for determining an order of performance for the assays ordered for the samples.

A sample dispensing mechanism configured to dispense a sample and a reagent to the reaction vessel at a first dispensing position and the reaction cell positioned at a second dispensing position; a second reagent vessel disposed on a track of the sample dispensing mechanism; and a control unit configured to control the sample dispensing mechanism, in which the control unit is configured to, based on information on presence or absence of incubation of an analysis item, control the sample dispensing mechanism to dispense a sample and a reagent to the reaction vessel positioned at the first dispensing position in a case where the incubation is not required by the analysis item, and control the sample dispensing mechanism to dispense a sample to the reaction cell positioned at the second dispensing position in a case where the incubation is required by the analysis item.

Aspects of the present disclosure include methods and systems for automated analysis of clinical fluid samples, such as urine, blood, or cerebral spinal fluid, where the number of fluid samples in increased or optimized without negatively impacting the accuracy of the analysis of a given fluid sample.

The invention has an object to provide an automatic analyzer and a control program that can shorten total analysis time. The automatic analyzer comprises: a sample rack that houses a sample; a sample dispensing mechanism that aspirates the sample from the sample rack and dispenses the sample into a reaction container; a plurality of detection units that detect a reaction liquid in the reaction container; and a control unit that controls the sample dispensing mechanism and the detection units. The control unit checks the measurement item specified for the sample and checks one of the detection units that is specified by the measurement item. When measurements specifying the same detection unit among the detection units are specified consecutively, the order of dispensing by the sample dispensing mechanism is changed so that measurements specifying different detection units are made consecutively.

A sample testing system includes a test receptacle support structure, an optical element positioned for transmitting electromagnetic radiation emitted or reflected by a sample disposed in a test receptacle supported by the test receptacle support structure, a cleaning member, and an automated transport arm configured to (i) detachably couple the cleaning member, (ii) move the detachably-coupled cleaning member into a position proximate to and/or contacting the optical element, and (iii) decouple the cleaning member.

Disclosed are high-throughput vessel supply systems and methods of supplying sample vessels, such as samples stored in test tubes. A system for supplying a plurality of individual vessels that each contains a sample is disclosed.