| 1. |
|
|
| 2. |
- Jordan, R, et al.
(författare)
-
Nested convolutional codes and their application to woven codes
- 2004
-
Ingår i: IEEE Transactions on Information Theory. - 0018-9448. ; 50:2, s. 380-384
-
Tidskriftsartikel (refereegranskat)abstract
- Nested convolutional codes are a set of convolutional codes that is derived from a given generator matrix. The structural properties of nested convolutional codes and nested generator matrices are studied. A method to construct the set of all minimal (rational) generator matrices of a given convolutional code is presented. As an example, two different sets of nested convolutional codes are derived from two equivalent minimal generator matrices. The significant difference in their free-distance profiles emphasizes the importance of being careful when selecting the generator matrices that determine the nested convolutional codes. As an application of nested convolutional codes, woven codes with outer warp, and inner nested convolutional codes are considered. The free-distance profile of the inner generator matrix is shown to be an important design tool.
|
|
| 3. |
- Jordan, R, et al.
(författare)
-
Woven convolutional codes II: Decoding aspects
- 2004
-
Ingår i: IEEE Transactions on Information Theory. - 0018-9448. ; 50:10, s. 2522-2529
-
Tidskriftsartikel (refereegranskat)abstract
- An iterative decoding scheme for woven convolutional codes is presented. It operates in a window sliding over the received sequence. This exploits the nature of convolutional codewords as infinite sequences and reflects the concept of considering convolutional encoding and decoding as a continuous process. The decoder is analyzed in terms of decoding delay and decoding complexity. Its basic building block is a symbol-by-symbol a posteriori probability (APP) decoder for convolutional codes, which is a windowed variant of the well-known Bahl-Cocke-Jelinek-Raviv (BCJR) algorithm. Additional interleaving for the woven constructions is introduced by employing convolutional scramblers. It is shown that row-wise random interleaving preserves the lower bound on the free distance of the original woven constructions. Based on the properties of the interleavers, new lower bounds on the free distance of woven constructions with both outer warp and inner warp are derived. Simulation results for woven convolutional codes with and without additional interleaving are presented.
|
|
| 4. |
- Jordan, Ulf, 1974, et al.
(författare)
-
Microwave breakdown in slots
- 2004
-
Ingår i: IEEE Trans. Plasma Science. ; 32, s. 2250-
-
Tidskriftsartikel (refereegranskat)
|
|
| 5. |
- Lehmann, O. J., et al.
(författare)
-
Novel anterior segment phenotypes resulting from forkhead gene alterations: Evidence for cross-species conservation of function
- 2003
-
Ingår i: Investigative Ophthalmology & Visual Science. - : Association for Research in Vision and Ophthalmology (ARVO). - 0146-0404 .- 1552-5783. ; 44:6, s. 2627-2633
-
Tidskriftsartikel (refereegranskat)abstract
- PURPOSE. Mutations in murine and human Versions of an ancestrally related gene usually result in similar phenotypes. However, interspecics differences exist, and in the case of two forkhead transcription factor genes (FOXC1 and FOXC2), these differences include corneal or anterior segment phenotypes, respectively. This study was undertaken to determine whether such discrepancies provide an opportunity for identifying novel human-murine ocular phenotypes. METHODS. Four pedigrees with early-onset glaucoma phenotypes secondary to segmental chromosomal duplications or deletions encompassing FOXC1 and 18 individuals from 9 FOXC2 mutation pedigrees underwent detailed ocular phenotyping. Subsequently, mice with mutations in Foxc1 or a related forkhead gene, Foxe3, were assessed for features of the human phenotypes. RESULTS. A significant increase in central corneal thickness was present in affected individuals from the segmental duplication pedigrees compared with their unaffected relatives (mean increase 13%, maximum 35%, P < 0.05). Alterations in corneal thickness were present in mice heterozygous and homozygous for Foxe3 mutations but neither in Foxc1 heterozygotes nor the small human segmental deletion pedigree. Mutations in FOXC2 resulted in ocular anterior segment anomalies. These were more severe and prevalent with mutations involving the forkhead domain. CONCLUSIONS. Normal corneal development is dependent on the precise dose and levels of activity of certain forkhead transcription factors. The altered corneal thickness attributable to increased forkhead gene dosage is particularly important, because it may affect the clinical management of certain glaucoma subtypes and lead to excessive treatment. The FOXC1 and Foxe3 data, taken together with the novel ocular phenotypes of FOXC2 mutations, highlight the remarkable cross-species conservation of function among forkhead genes.
|
|
| 6. |
|
|
