Abstract:
The invention relates to a test tube of the type that are used for chemical and biological analysis, having an approximate shape of a cylinder or a truncated cone, comprising an opening in the upper region thereof for inserting substances, and formed from a single piece of a homogeneous material with a translucent colour, composed of a mixture of a polymer from the family of metallocene polyolefins, that homogeneously contains a polypropylene-based masterbatch of a laser-sensitive additive that changes colour to a different contrasting colour, for example an approximately brown-black colour, when exposed to the excitation of a laser marker.
Abstract:
Devices having nanochannels suitable for confinement and alignment of DNA molecules, as well as methods of fabricating the same and methods of using the same for DNA analysis, are provided. A device can include a dynamically-controlled, unified microchannel-nanochannel platform suitable for confinement and alignment of DNA molecules. The nanochannels can be reversibly formed within nanoslits formed in a deformable substrate or base layer.
Abstract:
A method of collecting test data from use of a disposable test kit, the method comprising the steps of: a code reader scanning a unique test identifier provided on the disposable test kit; an identification module identifying from the scanned unique test identifier a type of test performed by the disposable test kit; the code reader scanning a patient identifier; the identification module identifying from the scanned patient identifier a patient who has used the disposable test kit; a display and selection module automatically displaying on a display screen each of all possible distinct outcomes associated with the identified test as a selectable option; a user selecting one of the displayed all possible distinct outcomes for collection as test data; an association module automatically associating the test data with the patient; and the user activating storage of the test data to a data storer.
Abstract:
Embodiments of the invention provide a filter kit including filters for processing a biological sample. Some embodiments include a filter cap in a tube kit with a first tube containing a buffer solution and a second tube containing a lyophilized master mix. Some embodiments include a method of processing a sample using the kit including mixing a biological sample in a first tube with the buffer solution, positioning the filter cap in the first tube, positioning a second tube on the filter cap, flipping the first tube, the filter cap, and the second cap to filter the biological sample and buffer solution mixture with the filter cap as it flows from the first tube to the second tube. Some embodiments include structure enabling transfer of materials through inline flow between the tubes. Some further embodiments include integrated structure for sample pulverization with integrated buffer and lyophilized master mix.
Abstract:
Non-uniformities in substrate thickness and surface topography contribute significantly to the need for auto-focusing on a sample deposited thereon. These auto- focusing needs can be reduced or eliminated by measuring and storing substrate surface topography for later retrieval by an imaging system that can use the topographic information to help set appropriate focal parameters. These steps can be done in advance of an imaging experiment to reduce focus-related delays during the experiment. Topographic information can be stored, for example, in a database, associated with a representation of a unique substrate identifier; entry of the representation retrieves the topographic information. As another example, topographic information can be stored in an encoding device associated with the substrate.
Abstract:
Methods and devices for analysing blood sample volumes are provided. In particular, the disclosure provides a method for estimating the volume of a blood sample on a substrate including the steps of acquiring an image of the blood sample. A coverage or area of the blood sample may be obtained from the image and compared to a standard curve to obtain a volume estimate of the blood sample. The disclosure also proves a device for scanning one or more blood samples on a substrate. The device includes three layers that may be assembled to hold multiple samples between the layers. The device also includes labels and may be disassembled for decontamination and reloading of samples.
Abstract:
Microfluidic methods for barcoding nucleic acid target molecules to be analyzed, e.g., via nucleic acid sequencing techniques, are provided. Also provided are microfluidic, droplet-based methods of preparing nucleic acid barcodes for use in various barcoding applications. The methods described herein facilitate high-throughput sequencing of nucleic acid target molecules as well as single cell and single virus genomic, transcriptomic, and/or proteomic analysis/profiling. Systems and devices for practicing the subject methods are also provided.
Abstract:
Diagnostic devices; systems, methods and computer-readable media store instructions related to determining hemoglobin information using those devices. The methods may include processing a captured image of the reservoir and/or device and the device information to determine color information for the solution and the scale, the color information including one or more color attributes; adjusting the color information for the solution based on the color information for the scale; and determining hemoglobin information (e.g., hemoglobin level, disease state and/or calculated hematocrit) based on the adjusted color information and a stored profile information associated with the device information.
Abstract:
A biological sample containment system (10) that includes a biological specimen collection container (12) for collecting a biological sample and a label (20) for the container (12) is disclosed. In one embodiment, the label (20) includes a first or front side(22) and a second or rear side (24) having a readable information portion (26). The label (20) is affixable to the container (12) by the second side (24) and with the label (20) affixed to the container (12), the readable information portion (26) on the second side (24) is readable through a portion of the container (12). By including readable information on the second or rear side (24) of the label (20), the amount of readable information that can be included on the label (20) is increased by using the previously unused rear side of the label (20).