Abstract:
Both a chalcogenide select device and a chalcogenide memory element are formed within vias within dielectrics. As a result, the chalcogenides is effectively trapped within the vias and no glue or adhesion layer is needed. Moreover, delamination problems are avoided. A lance material is formed within the same via with the memory element. In one embodiment, the lance material is made thinner by virtue of the presence of a sidewall spacer; in another embodiment no sidewall spacer is utilized. A relatively small area of contact between the chalcogenide used to form a memory element and the lance material is achieved by providing a pin hole opening in a dielectric, which separates the chalcogenide and the lance material.
Abstract:
A microfluidic device for nucleic acid analysis includes a monolithic semiconductor body (13), a microfluidic circuit (10), at least partially accommodated in the monolithic semiconductor body (13), and a micropump (11). The microfluidic circuit (10) includes a sample preparation channel (18) formed on the monolithic semiconductor body (13) and at least one microfluidic channel (20, 22) buried in the monolithic semiconductor body (13). The micropump (11), includes a plurality of sealed chambers (40) provided with respective openable sealing elements (41) and having a first pressure therein that is different from a second pressure in the microfluidic circuit (10). In addition, the micropump (11) and the microfluidic circuit (10) are configured so that opening the openable sealing elements (41) provides fluidic coupling between the respective chambers (40) and the microfluidic circuit (10). The openable sealing elements (41) are integrated in the monolithic semiconductor body (13).
Abstract:
A plurality of planar electrodes (5) in a microchannel (4) is used for separation, lysis and PCR in a chip (10). Cells from a sample are brought to the electrodes (5). Depending on sample properties, phase pattern, frequency and voltage of the electrodes and flow velocity are chosen to trap target cells (16) using DEP, whereas the majority of unwanted cells (17) flushes through. After separation the target cell (16) are lysed while still trapped. Lysis is carried out by applying RF pulses and/or thermally so as to change the dielectric properties of the trapped cells. After lysis, the target cells (16) are amplified within the microchannel (4), so as to obtain separation, lysis and PCR on same chip (1).
Abstract:
In the MSN encoded form, the symbols of each block of the present invention define a running digital sum (RDS) value, defined as RDS([a0a1 . . . aN−1])=−Σi(−1)ai where the symbols ai belong to the set {0, 1} and the sum extends for values of i from 0 to N−1. An encoder is configured to satisfy at least one of the following characteristics: a) blocks of symbols with a given length (L) are used for encoding, wherein RDS=RDS0+4.K, where K is an integer, RDS is the said running digital sum, RDS0 is defined as zero for even values of the said length (L), and one for odd values of said length (L), and b) blocks of symbols with a given length (L) are used for MSN coding and encoding is effected by selecting encoded blocks such that the set of running digital sum (RDS) values is the set with the minimum number of elements that satisfy the required rate value, defined as the ratio between the length of the input blocks and the length of the output blocks. A decoder with a simplified trellis structure is used for decoding (as in decoding a digital signal read from media on which the signal in question has been recorded via a vertical or perpendicular magnetic recording technique, for example).