Abstract: A microfluidic lab-on-a-chip system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The lab-on-a-chip has a fluidic platform with a plurality of arrays operably connected to a voltage source and a controller for the voltage source, a set of first inlets operably connected to the fluidic platform, each first inlet for one DNA symbol from a DNA symbol library, a set of second inlets operably connected to the fluidic platform, each second inlet for one DNA linker from a DNA linker library, and a mixing area operably connected to the fluidic platform and to the plurality of first inlets and the plurality of second inlets.

Abstract: An edge node has a central processing operable to gather sensor node data via a sensor and store at least part of the sensor node data locally in a public region of a persistent storage. The edge node backs up duplicate portions of the sensor node data to public storage regions of peer-edge nodes. The edge node receives private data from a host that is coupled to the edge computing node and the peer edge nodes, and stores the private data in a private region of the persistent storage. The private region is protected from the peer edge nodes using distributed key management.

Abstract: A method for reducing noise in a read signal due attributable to read element asymmetry provides for transmitting a write signal through a write precompensation circuit that shifts rising edges and falling edges of each of pulse in the write signal by a select magnitude and in opposite directions. After the write signal is encoded on a media, a corresponding read signal is read, with a read element, from the media. The method further provides for transmitting the read signal through a magnetoresistive asymmetry compensation (MRAC) block that is tuned to correct second-order non-linearities characterized by a particular set of distortion signatures. The select magnitude of the waveform shift applied by the write precompensation circuit introduces a non-linear signal characteristic that combines with non-linear signal characteristics introduced by the read element to generate one of the particular distortion signatures that is correctable by the MRAC block.

Abstract: Building DNA strands at a high rate that are suitable for data storage. Methods include using DNAzyme and utilizing libraries of pre-prepared oligos. A system for the DNA strand synthesis includes: a DNA symbol library comprising a number of single strand oligo symbols; a DNA linker library comprising a first set of single strand oligo linkers and a second set of single strand oligo linkers; and a DNAzyme library comprising a number of DNAzymes. An S1 end of a first DNAzyme is adapted to join the S1 end of a symbol and an S2 end of the first DNAzyme is adapted to join an S2 end of a first linker, and an S1 end of a second DNAzyme is adapted to join an S1 end of a second linker and an S2 end of the second DNAzyme is adapted to join an S2 end of the symbol.

Abstract: A controller extracts a distortion component of a readback signal from a magnetic read head. The distortion component may be found using a finite length Volterra series, for example. The controller estimates a clearance between the read head and a recording medium based on the distortion component. This clearance measurement can be used for closed loop fly-height control of the read head.

Abstract: A method for reducing noise in a read signal due attributable to read element asymmetry provides for transmitting a write signal through a write precompensation circuit that shifts rising edges and falling edges of each of pulse in the write signal by a select magnitude and in opposite directions. After the write signal is encoded on a media, a corresponding read signal is read, with a read element, from the media. The method further provides for transmitting the read signal through a magnetoresistive asymmetry compensation (MRAC) block that is tuned to correct second-order non-linearities characterized by a particular set of distortion signatures. The select magnitude of the waveform shift applied by the write precompensation circuit introduces a non-linear signal characteristic that combines with non-linear signal characteristics introduced by the read element to generate one of the particular distortion signatures that is correctable by the MRAC block.

Abstract: A microfluidic device for polymerase chain reaction (PCR) processing includes a platform with a microstructure with at least one reaction chamber, and a heating element. The heating element heats at least a part of the at least one reaction chamber. The heating element includes at least one spin torque oscillator (STO) configured to heat the at least a part of the at least one reaction chamber to one or more temperatures for PCR processing.

Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first end and a second end and a second linker of the pair having a first end and a second end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.

Abstract: Method and apparatus for generating and processing pulses in a light detection and ranging (LiDAR) system. In some embodiments, an emitter outputs phase modulated continuous wave (PMCW) light sequences encoded with a selected encoding scheme such as a pseudo-random bit sequence (PRBS). An analog processing circuit processes reflected light sequences from a target illuminated by the PMCW light sequences by performing analog extraction of a doppler component and analog encoding correlation prior to digitalization of the received signal. The analog processing circuit can include a plurality of demodulation stages each multiplying the input signals by positive and negative magnitudes of a scalar value at times corresponding to signal transitions of different associated doppler clock frequencies.

Abstract: An optical receiver includes a parasitic current compensation circuit having a reference diode, a sense avalanche photodiode (APD), at least one DC voltage source, and a measurement node. The at least one DC voltage source is configured to generate a first DC bias voltage that varies over time and drives the reference diode, and generates a second DC bias voltage that varies over time and drives the sense APD. A reference parasitic current travels through the reference diode based on the first DC bias voltage. A sense current travels through the sense APD based on the second DC bias voltage and exposure of the sense APD to a light signal. The measurement node receives a sense photocurrent, which is generated by the sense APD in response to the exposure of the sense APD to the light signal, the sense photocurrent including the sense current less the reference parasitic current.

Abstract: Apparatus and method for adaptively adjusting amplifier gain based on detected distance to a target in a light detection and ranging (LiDAR) system. In some embodiments, the amplifier amplifies detected pulses obtained from a photodetector, and the gain is adjusted from among at least two selectable gain modes responsive to a measured time of flight (ToF) for the pulses. A first range of gain levels can be used for targets that are within a first maximum distance range, and a second range of gain levels can be used for targets that are beyond the first maximum distance range. Each mode can extend from a minimum to a maximum value along a selected linear slope. A gain adjustment circuit can use a Gilbert Cell or a multiplier and fully differential amplifier arrangement.

Abstract: A microfluidic device for polymerase chain reaction (PCR) processing includes a platform with a microstructure with at least one reaction chamber, and a heating element. The heating element heats at least a part of the at least one reaction chamber. The heating element includes at least one spin torque oscillator (STO) configured to heat the at least a part of the at least one reaction chamber to one or more temperatures for PCR processing.

Abstract: Methods and systems for use in reading DNA storage genes generally include removing one or more linking symbols from a first strand of a DNA storage gene, introducing a test symbol pool to the DNA storage gene, and replacing a data symbol in the first strand of the DNA storage gene with a single stranded test symbol from the test symbol pool when the linking symbol and data symbol of the single stranded test symbol are complimentary to an adjacent linking symbol and data symbol in the second strand of the DNA storage gene. The DNA storage gene is then scanned to identify locations on the DNA storage gene where the linking symbol is double stranded or single stranded. The locations where double stranded linking symbols are detected are then used, along with the composition of the test symbol pool, to read the DNA storage gene.

Abstract: Systems and methods are disclosed for a multiple detector data channel and data detection utilizing different cost functions. For example, a digital data channel system can have multiple data detectors where each data detector implements a distinct cost function for detecting data. A cost function analyzer can then selectively choose decisions from the multiple data detectors to generate a data sequence. In some examples, a dual detector system may have one detector implement a Soft-Output Viterbi Algorithm (SOVA) cost function and another detector implement a peak detection algorithm. Further, in some embodiments, the cost function analyzer can implement multiple selection criteria to determine which decisions to include in a data sequence from the multiple data detectors.

Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first end and a second end and a second linker of the pair having a first end and a second end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.

Abstract: An edge node has a central processing operable to gather sensor node data via a sensor and store at least part of the sensor node data locally in a public region of a persistent storage. The edge node backs up duplicate portions of the sensor node data to public storage regions of peer-edge nodes. The edge node receives private data from a host that is coupled to the edge computing node and the peer edge nodes, and stores the private data in a private region of the persistent storage. The private region is protected from the peer edge nodes using distributed key management.

Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first overhanging end and a second overhanging end and a second linker of the pair having a first overhanging end and a second overhanging end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.

Abstract: An apparatus includes a write pole that stores data on tracks on a data storage medium. The apparatus also includes side shields on first and second sides of the write pole, and a trailing shield above the write pole and above the side shields. The apparatus further includes a microwave assisted magnetic recording oscillator having conductive pads that form capacitors with portions of a conductive film of the data storage medium. The conductive pads are positioned on a medium-facing surface of a slider that includes the write pole, the side shields and the trailing shield.

Abstract: One or more networks each include a plurality of sensor nodes operable to communicate public data with each other. Each of the plurality of sensor nodes is operable to gather sensor node data and store the sensor node data locally on the sensor node. Duplicate portions of the sensor node data are distributed to the public data of others of the plurality of sensor nodes via the public data paths for backup storage. The system includes a host that is coupled to individually communicate private data with each of the plurality of sensor nodes. Each of the sensor nodes protects the private data from others of the sensor nodes using distributed key management to ensure distributed encryption.

Abstract: A system for DNA gene assembly that utilizes a DNA symbol library and a DNA linker library. The symbol library has a number of DNA symbols each having a first overhanging end and a second overhanging end different than and non-complimentary to the first end, the first and second ends being the same nucleotides for each DNA symbol. The linker library has pairs of DNA linkers, a first linker of a pair having a first overhanging end and a second overhanging end and a second linker of the pair having a first overhanging end and a second overhanging end, the first end of the first linker being the same nucleotides for each first linker and the second end of the second linker being the same nucleotides for each second linker, wherein the second end of the first linker and the first end of the second linker have complementary nucleotides. The first linker joins to the first end of a DNA symbol and the second linker joins to the second end of another DNA symbol.