Abstract: A combined error checker and sequence generator which shares a LFSR is disclosed which reduces complexity, cost, and area required for implementation while also improving timing margin. A clock and data recovery system recovers a data signal received over a channel from a remote transceiver. Control logic selects different modes of operation of the system. An error detector compares the two sequence signals and records errors in response to differences between the two sequence signals. A sequence generator generates a sequence signal for use by the error detector as a reference sequence signal or for transmission to a remote transceiver. The system includes one or more switching elements configured to selectively route the generated sequence as feedback into the sequence generator or the received sequence signal into the sequence generator subject to whether the combined error checker and sequence generator is in error checker mode or sequence generator mode.

Abstract: A combined error checker and sequence generator which shares a LFSR is disclosed which reduces complexity, cost, and area required for implementation while also improving timing margin. A clock and data recovery system recovers a data signal received over a channel from a remote transceiver. Control logic selects different modes of operation of the system. An error detector compares the two sequence signals and records errors in response to differences between the two sequence signals. A sequence generator generates a sequence signal for use by the error detector as a reference sequence signal or for transmission to a remote transceiver. The system includes one or more switching elements configured to selectively route the generated sequence as feedback into the sequence generator or the received sequence signal into the sequence generator subject to whether the combined error checker and sequence generator is in error checker mode or sequence generator mode.

Abstract: Transmit amplitude independent adaptive equalizers are provided that compensate for transmission losses in an input signal when the transmit signal amplitude is unknown. Several embodiments are provided, including a first embodiment having an equalizer core, a controllable-swing slicer and an amplitude control loop, a second embodiment having an equalizer core, a fixed-swing slicer and a control loop, a third embodiment having an equalizer core, a variable gain amplifier, and a variable gain amplifier control loop, and a fourth embodiment having an equalizer core, a fixed-swing slicer, a variable gain amplifier, and a variable gain amplifier control loop.

Abstract: Transmit amplitude independent adaptive equalizers are provided that compensate for transmission losses in an input signal when the transmit signal amplitude is unknown. Several embodiments are provided, including a first embodiment having an equalizer core, a controllable-swing slicer and an amplitude control loop, a second embodiment having an equalizer core, a fixed-swing slicer and a control loop, a third embodiment having an equalizer core, a variable gain amplifier, and a variable gain amplifier control loop, and a fourth embodiment having an equalizer core, a fixed-swing slicer, a variable gain amplifier, and a variable gain amplifier control loop.

Abstract: Transmit amplitude independent adaptive equalizers are provided that compensate for transmission losses in an input signal when the transmit signal amplitude is unknown. Several embodiments are provided, including a first embodiment having an equalizer core, a controllable-swing slicer and an amplitude control loop, a second embodiment having an equalizer core, a fixed-swing slicer and a control loop, a third embodiment having an equalizer core, a variable gain amplifier, and a variable gain amplifier control loop, and a fourth embodiment having an equalizer core, a fixed-swing slicer, a variable gain amplifier, and a variable gain amplifier control loop.

Abstract: The present invention provides a variant of an immunoglobulin variable domain including (A) at least one CDR region and (B) framework regions flanking the CDR region, wherein the variant also contains (a) a CDR region having added or substituted therein at least on binding sequence and (b) the flanking framework regions, wherein the binding sequence is heterelogous to the CDR and is an antigenic sequence from a MUC-1 binding sequence.