Results 71 to 80 of about 4,090,293 (192)

Mapping optical process in semiconductor nanowires using dynamic optical tweezers

, 2016
We present a novel method for spatial mapping of the luminescent properties of single optically trapped semiconductor nanowires by combing dynamic optical tweezers with micro-photoluminescence. The technique involves the use of a spatial light modulator (
McGloin, David, Jagadish, Chennupati, Ming Lee, Woei, Reece, Peter, Tan, Hark Hoe, Gao, Qiang, Wang, Fan, Hartstone, Alexander, Toe, Wen Jun   +8 more
core   +1 more source

Performance optimization of free-space optical communication protocols based on results from FSO demonstrations [PDF]

, 2007
The mobile free-space optical channel mainly suffers from relatively long link outages, produced by short-term blockings of the line-of-sight (obstacles, clouds), pointing- and tracking-errors or deep signal-fades caused by index of refraction turbulence
Bernhard Epple, Epple, Bernhard
core   +1 more source

BiSCoT: Improving large eukaryotic genome assemblies with optical maps

PeerJ, 2019
ABSTRACT Motivation Long read sequencing and Bionano Genomics optical maps are two techniques that, when used together, make it possible to reconstruct entire chromosome or chromosome arms structure. However, the existing tools are often too conservative and organization of contigs into scaffolds is ...
Istace, Benjamin, Belser, Caroline, Aury, Jean-Marc   +2 more
openaire   +4 more sources

The distribution of D4Z4 repeats in China and direct prenatal diagnosis of FSHD by optical genome mapping

Orphanet Journal of Rare Diseases
Background Facioscapulohumeral muscular dystrophy (FSHD) is the second most common form of muscular dystrophy, which is characterized by a reduction in the number of D4Z4 repeats on chromosome 4q35.
Mengmeng Li, Na Hao, Jiazhen Chang, Kaili Yin, Xueting Yang, Yaru Wang, Yi Dai, Yulin Jiang   +7 more
doaj   +1 more source

Structural variation in the chicken genome identified by paired-end next-generation DNA sequencing of reduced representation libraries [PDF]

, 2011
Background Variation within individual genomes ranges from single nucleotide polymorphisms (SNPs) to kilobase, and even megabase, sized structural variants (SVs), such as deletions, insertions, inversions, and more complex rearrangements.
Kerstens Hindrik HD, Vereijken, A., Martien AM Groenen, Bert W Dibbits, Groenen, M.A.M., Dibbits, B.W., Kerstens, H.H.D., Dibbits Bert W, Okimoto Ron, Hindrik HD Kerstens, Richard PMA Crooijmans, Addie Vereijken, Vereijken Addie, Crooijmans, R.P.M.A., Okimoto, R., Groenen Martien AM, Crooijmans Richard PMA, Ron Okimoto   +17 more
core   +2 more sources

Optical Mapping: Detecting Genomic Resistance Cassettes in MRSA

ACS Omega
Methicillin-resistant Staphylococcus aureus (MRSA) is a multidrug-resistant bacterium with a global presence in healthcare facilities as well as community settings. The resistance of MRSA to beta-lactam antibiotics can be attributed to a mobile genetic element called the staphylococcal cassette chromosome mec (SCCmec), ranging from 23 to 68 kilobase ...
Ruppeka-Rupeika, E., Abakumov, S., Engelbrecht, M., Chen, X., do Carmo Linhares, D., Bouwens, A., Leen, V., Hofkens, J., Hofkens, J.   +8 more
openaire   +5 more sources

Optical Genome Mapping Identifies a Novel Unbalanced Translocation Between Chromosomes 4q and 6q Leading to Feeding Difficulties and Hypotonia in a Neonate: A Case Report

The Application of Clinical Genetics
Ying Wang, Shaohua Bi, Xiaoqing Shi, Liying Dai Division of Neonatology, Anhui Provincial Children’s Hospital, Hefei, Anhui, 230051, People’s Republic of ChinaCorrespondence: Liying Dai, Division of Neonatology, Anhui Province Children’s Hospital, No. 39,
Wang Y, Bi S, Shi X, Dai L
doaj  

Optical genome mapping (Bionano – Saphyr) for AML associated with cryptic chromosomal recurrent abnormality

peer reviewedHere, we report the diagnostic work-up of a thirty-three-year-old woman presenting with 77% bone marrow myeloid blasts. Conventional cytogenetic did not show any recurrent abnormality but four mutations were found in three genes: FLT3, CEBPA
Beckers, Pablo, KOOPMANSCH, Benjamin, Franke, Sabine, MENTEN, Catherine, Catarin, Nicolas, JAMAR, Mauricette, Fernandez Carazo, Rafael, LLORENTE, William, LETE, Céline, Bours, Vincent, Lambert, Frédéric, GUADAGNI, Alexandra   +11 more
core  

[New Guinea, scale 1:63,360] [cartographic material] /

, 1955
Provisional ed. Uncontoured (planimetric) map series of Papua New Guinea, compiled from aerial photography, showing minor roads, tracks, water features, buildings and populated places. Relief shown by spot heights.; Produced by National Mapping Office to
Australia. National Mapping Office.
core  

Optical genome mapping unveils hidden structural variants in neurodevelopmental disorders

Scientific Reports
While short-read sequencing currently dominates genetic research and diagnostics, it frequently falls short of capturing certain structural variants (SVs), which are often implicated in the etiology of neurodevelopmental disorders (NDDs).
Isabelle Schrauwen, Yasmin Rajendran, Anushree Acharya, Susanna Öhman, Maria Arvio, Ritva Paetau, Auli Siren, Kristiina Avela, Johanna Granvik, Suzanne M. Leal, Tuomo Määttä, Hannaleena Kokkonen, Irma Järvelä   +12 more
doaj   +1 more source