• 한국HCI학회:학술대회논문집
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• 한국HCI학회 2009년도 학술대회
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• pp.558-561
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• 2009

본 논문에서는 증강현실에서 마커에 포함된 이미지뿐만 아니라 문자 인식을 지원하기 위한 심플 프레임 마커를 제안한다. 마커 내부에 임의의 패턴 대신에 문자를 삽입하고 문자 인식 알고리즘(Optical Character Recognition)을 사용하여 인식하면 실행 전 학습과정이 필요 없을 뿐만 아니라 문자의 친숙함 때문에 시각적 장애요인도 줄일 수 있다. 따라서 기존의 마커 방식인 이미지뿐만 아니라 문자도 인식하기 위해서 제안된 심플 프레임 마커는 정의된 마커의 가로세로 비율에 따라 이미지타입의 마커(Square SFMarker)인지 문자타입의 마커(Rectangle SFMarker)인지를 구별하고 각기 다른 인식 알고리즘을 적용한다. 또한 문자 인식을 위한 전처리 과정을 줄이기 위해 디자인 단계에서 마커 테두리에 방향정보를 삽입하고, 인식 단계에서는 이 방향 정보를 추출하여 문자 인식을 빠르고 정확하게 수행한다. 마지막으로 매 프레임 문자를 인식하는 알고리즘을 수행 시 추적 속도가 저하되므로, 프레임간 변화량이 적을 때는 이전 프레임의 인식 결과 정보를 사용하여 수행 속도를 높인다.

• 한국수산과학회지
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• 제49권6호
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• pp.867-874
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• 2016

Although shrimps belonging to family Crangonidae are known to be genetically divergent and ecologically important among the various benthos, any of their mitochondrial genome has not been reported yet. We here determined the complete mitochondrial genome sequence of Crangon hakodatei (Rathbun, 1902), which was collected from East China Sea ($124^{\circ}E$ and $34.5^{\circ}N$). Total mitochondrial genome length of C. hakodatei was 16,060 bp, in which 13 proteins, 2 ribosomal RNAs, 22 transfer RNAs and a putative control region were encoded. Secondary structure prediction analysis showed that twenty tRNA genes exhibit the conserved structure but two genes, $tRNA^{Cys}$ and $tRNA^{Ser}$ (AGN), lack T and D arm, respectively. Based on the sequence similarity of the COI region from the currently reported five species belonging to genus Crangonidae, C. hakodatei was most closely related to Crangon crangon. Phylogenetic analysis of full COXI genes belonging to infraorder Caridea showed that only crangonid shrimps were clustered together with those of Dendrobranchiata. Gene order were well conserved from Penaeoidea to Caridea but $tRNA^{Pro}$ and $tRNA^{Thr}$ in Palaemonid shrimp were flipped each other by the recombination. Further study about mitochondrial genome sequences of shrimps belonging to Crangonidae should be made to know better about their evolutional relationships with other those in infraorder Caridea.

• Genomics & Informatics
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• 제21권3호
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• pp.39.1-39.15
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• 2023

DNA barcoding without assessing reliability and validity causes taxonomic errors of species identification, which is responsible for disruptions of their conservation and aquaculture industry. Although DNA barcoding facilitates molecular identification and phylogenetic analysis of species, its availability in clariid catfish lineage remains uncertain. In this study, DNA barcoding was developed and validated for clariid catfish. 2,970 barcode sequences from mitochondrial cytochrome c oxidase I (COI) and cytochrome b (Cytb) genes and D-loop sequences were analyzed for 37 clariid catfish species. The highest intraspecific nearest neighbor distances were 85.47%, 98.03%, and 89.10% for COI, Cytb, and D-loop sequences, respectively. This suggests that the Cytb gene is the most appropriate for identifying clariid catfish and can serve as a standard region for DNA barcoding. A positive barcoding gap between interspecific and intraspecific sequence divergence was observed in the Cytb dataset but not in the COI and D-loop datasets. Intraspecific variation was typically less than 4.4%, whereas interspecific variation was generally more than 66.9%. However, a species complex was detected in walking catfish and significant intraspecific sequence divergence was observed in North African catfish. These findings suggest the need to focus on developing a DNA barcoding system for classifying clariid catfish properly and to validate its efficacy for a wider range of clariid catfish. With an enriched database of multiple sequences from a target species and its genus, species identification can be more accurate and biodiversity assessment of the species can be facilitated.