32 results about "Systematic variation" patented technology

The invention relates to systems for a transmission of images via channels of communication with a limited capacity by means of application of compression of the images. The technical result consists in an increase of the compression degree upon encoding, and it allows to fulfill the transmission of such encoded images via the channel of communication with the limited capacity, therewith a high degree of the compression is provided without of increase of computational power of encoding device and without of distortions upon decoding. The result is obtained by the usage of more effective method of interpolation of restored subsamples, in this method there is used an adaptive and applicative set of samples, which restore a quantized signal, and this set of the samples allows to improve an accuracy of the interpolation with a number of the subsamples, which is necessary for the right interpolation that is simultaneously decreased one.

An acoustic borehole logging system for parameters of a well borehole environs. Full wave acoustic response of a scanning transducer is used to measure parameters indicative of condition of a tubular lining the well borehole, the bonding of the tubular to material filling an annulus formed by the outside surface of the tubular and the wall of the borehole, the distribution of the material filling the annulus, and thickness of the tubular. A reference transducer is used to correct measured parameters for variations in acoustic impedance of fluid filling the borehole, and for systematic variations in the response of the scanning transducer. Corrections are made in real time. The downhole tool portion of the logging system is operated essentially centralized in the borehole using a centralizer that can be adjusted for operation in a wide range of borehole sizes.

A contour of a mask design for an integrated circuit is modified to compensate for systematic variations arising from non-optical effects such as stress, well proximity, rapid thermal anneal, or spacer thickness. Electrical characteristics of a simulated integrated circuit chip fabricated using the mask design are extracted and compared to design specifications, and one or more edges of the contour are adjusted to reduce the systematic variation until the electrical characteristic is within specification. The particular electrical characteristic preferably depends on which layer is to be fabricated from the mask: on-current for a polysilicon; resistance for contact; resistance and capacitance for metal; current for active; and resistance for vias. For systematic threshold voltage variation, the contour is adjusted to match a gate length which corresponds to an on-current value according to pre-calculated curves for contour current and gate length at a nominal threshold voltage of the chip.

Accurate characterization of microelectromechanical systems (MEMS) geometry is critical for device design and simulation, for material property extraction, and for post-fabrication trimming. According to the present embodiment, a method for characterizing parameters describing MEMS structures resulting from the fabrication process or process variations is presented. According to the prefered embodiment, experimentally obtained natural frequencies are compared with numerical simulations to identify unknown values of structural parameters or parameter variations. Further, the prefered embodiment teaches how electrostatically-driven laterally resonant comb-drive MEMS test structures with prescribed changes in spring width are used to characterize systematic variations in process offsets and sidewall angles. The disclosed technique is both in-situ and non-destructive.

The invention discloses a method for improving the sensitivity of detection in determining copy number variations. Disclosed are methods for determining copy number variation (CNV) known or suspected to be associated with a variety of medical conditions. In some embodiments, methods are provided for determining copy number variation (CNV) of fetuses using maternal samples comprising maternal and fetal cell free DNA. In some embodiments, methods are provided for determining CNVs known or suspected to be associated with a variety of medical conditions. Some embodiments disclosed herein provide methods to improve the sensitivity and/or specificity of sequence data analysis by removing within-sample GC-content bias. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples. Also disclosed are systems and computer program products for evaluation of CNV of sequences of interest.

Techniques that use the design databases used in each of the expose/etch steps during construction of phase shift masks are described. A model or reference image is rendered, accounting for systematic variations, from the design databases to represent what a layer of the PSM should look like after processing. The reference image is compared to an optically acquired image of a specimen phase shift mask to find defects. The technique of the present invention can be used to inspect EAPSM, APSM and tritone masks. The technique inspects all layers in one pass and is therefore more efficient.

Two paths (arrival and required paths) as a target of analysis are united into a single path, and an on-chip random variation component σr about a plurality of nodes of the single path is calculated. Next, an on-chip variation component σchip is calculated on the basis of the on-chip random variation component σr and an on-chip systematic variation component σs. Subsequently, a delay variation Docv is calculated on the basis of a reference delay Dbase of the entire path and the on-chip variation component σchip.

Methods for expressing active enzymes are described that involve co-expressing a first enzyme with a second enzyme that has an enzymatic activity that reverses a modification on the first enzyme and/or for identification of soluble and/or active catalytic domains by systematic variation of fragment lengths around catalytic domain boundaries.

A method is provided for using obtaining a reproducible device identifier from a physically unclonable function. An authentication device may receive a first physically unclonable function (PUF) dataset from the electronic device, the first PUF dataset including characteristic information generated from a physically unclonable function in the electronic device. The authentication device may then identify a pre-stored PUF dataset corresponding to the electronic device. Authentication of the electronic device may be performed by correlating the pre-stored PUF dataset and the first PUF dataset for the electronic device, wherein such correlation is based on a pattern or distribution correlation the pre-stored PUF dataset and the first PUF dataset. Because such correlation is performed on datasets, and not individual points, systematic variations can be recognized by the correlation operation leading to higher correlation than point-by-point comparisons.

A method, system and computer program product for determining a geometric parameter of an optical spot of a light beam are disclosed. A method comprises: providing a calibration target, the calibration target including a systematic variation in a parameter; measuring the calibration target with respect to the systematic variation using the light beam to obtain a plurality of measurements; and analyzing the measurements and the systematic variation to determine the geometric parameter of the optical spot.

Disclosed are methods for determining copy number variation (CNV) known or suspected to be associated with a variety of medical conditions, including syndromes related to CNV of subchromosomal regions wherein the bins from the unaffected training samples used as controls have a coverage similar to the coverage of the region inspected for CNV. In some embodiments, methods are provided for determining CNV of fetuses using maternal samples comprising maternal and fetal cell free DNA. Some embodiments disclosed herein provide methods to improve the sensitivity and/or specificity of sequence data analysis by removing within-sample GC-content bias. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples. In some embodiments, syndrome related biases in sample data are also removed to increase signal to noise ratio. Also disclosed are systems for evaluation of CNV of sequences of interest.

A system for visual encoding of words to assist learning to read including systematic variations in the appearance of letters which may look like morphic analogs of the sound variations they suggest (for example, barely visible grey for silent letters). By improving how letters cue sounds (like the alphabet originally did), visual encoding reduces the cognitive processing work that most impedes and endangers the progress of beginning and struggling readers (disambiguating letter-sound relationship confusion).

Disclosed are methods for determining copy number variation (CNV) known or suspected to be associated with a variety of medical conditions. In some embodiments, methods are provided for determining copy number variation (CNV) of fetuses using maternal samples comprising maternal and fetal cell free DNA. In some embodiments, methods are provided for determining CNVs known or suspected to be associated with a variety of medical conditions. Some embodiments disclosed herein provide methods to improve the sensitivity and/or specificity of sequence data analysis by deriving a fragment size parameter, such as a size-weighted coverage or a fraction of fragments in a size range. In some embodiments, the fragment size parameter is adjusted to remove within-sample GC-content bias. In some embodiments, removal of within-sample GC-content bias is based on sequence data corrected for systematic variation common across unaffected training samples. Also disclosed are systems and computer program products for evaluation of CNV of sequences of interest.

An airborne ultrasonic testing system includes two sets of ultrasound transmitters and receivers, an ultrasound frequency generator, a computer analyzer, and a controller. The ultrasound transmitters and opposing receivers are fixedly mounted at oblique angles from a support. A seal-receiving slot is defined between the transmitters and receivers, and is sized to receive a sealed edge portion of a container to be tested. The ultrasound transmitters preferably emit respective ultrasound streams that encounter a top surface of a sealed edge portion of the container at an angle between approximately 0-45 degrees, and most preferably, approximately 45 degrees. The angle of ultrasound emission of the first transmitter may be inverse of the angle of emission of the second transmitter. The signal response of each pair of receivers can be processed individually or combined to produce a summary test result of the two measurements that eliminates systematic variation associated with material variation.