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Sökning: WFRF:(Zhang Hanqing)

  • Resultat 1-10 av 28
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1.
  • Wang, Yu, et al. (författare)
  • A Novel MIMO-SAR Echo Separation Solution for Reducing the System Complexity : Spectrum Preprocessing and Segment Synthesis
  • 2023
  • Ingår i: IEEE Transactions on Geoscience and Remote Sensing. - 0196-2892. ; 61
  • Tidskriftsartikel (refereegranskat)abstract
    • The problem of echo separation using digital beamforming (DBF) on receive for multiple-input multiple-output (MIMO) synthetic aperture radar (SAR) is of notable importance to allow for practical systems. Regrettably, current DBF-MIMO-SAR schemes, such as the short-term shift-orthogonal (STSO) scheme, are computationally cumbersome, increasing the required hardware complexity. To alleviate this problem, we here propose an improved echo separation solution for realizing a low-cost MIMO-SAR system. We detail a generic waveform design scheme and optimized monostatic radar waveforms (e.g., nonlinear frequency modulation (NLFM) signal), showing how these can be directly adopted in the proposed scheme to improve imaging performance. The proposed scheme enables the number of interference segments generated by unmatched waveforms to be halved by the use of the fast time spectrum preprocessing and segment synthesis, dramatically simplifying the array configuration, and reduces the system complexity. By exploiting interpulse phase coding techniques, the proposed method can provide a reconfigurable waveform transmitting scheme, allowing the system resources in range frequency, elevation space, and Doppler domains to be jointly exploited for the separation of aliased signal returns. The proposed scheme is evaluated using extensive numerical and measured datasets, demonstrating the feasibility and potential of the proposed method for resource-limited spaceborne/airborne MIMO-SAR systems.
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2.
  • Dahlberg, Tobias, et al. (författare)
  • 3D printed water-soluble scaffolds for rapid production of PDMS micro-fluidic flow chambers
  • 2018
  • Ingår i: Scientific Reports. - : Nature Publishing Group. - 2045-2322. ; 8:1
  • Tidskriftsartikel (refereegranskat)abstract
    • We report a novel method for fabrication of three-dimensional (3D) biocompatible micro-fluidic flow chambers in polydimethylsiloxane (PDMS) by 3D-printing water-soluble polyvinyl alcohol (PVA) filaments as master scaffolds. The scaffolds are first embedded in the PDMS and later residue-free dissolved in water leaving an inscription of the scaffolds in the hardened PDMS. We demonstrate the strength of our method using a regular, cheap 3D printer, and evaluate the inscription process and the channels micro-fluidic properties using image analysis and digital holographic microscopy. Furthermore, we provide a protocol that allows for direct printing on coverslips and we show that flow chambers with a channel cross section down to 40 x 300 μm can be realized within 60 min. These flow channels are perfectly transparent, biocompatible and can be used for microscopic applications without further treatment. Our proposed protocols facilitate an easy, fast and adaptable production of micro-fluidic channel designs that are cost-effective, do not require specialized training and can be used for a variety of cell and bacterial assays. To help readers reproduce our micro-fluidic devices, we provide: full preparation protocols, 3D-printing CAD files for channel scaffolds and our custom-made molding device, 3D printer build-plate leveling instructions, and G-code.
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3.
  • del Pozo, Ana, et al. (författare)
  • Behavioral Characterization of dmrt3a Mutant Zebrafish Reveals Crucial Aspects of Vertebrate Locomotion through Phenotypes Related to Acceleration
  • 2020
  • Ingår i: eNeuro. - 2373-2822. ; 7:3
  • Tidskriftsartikel (refereegranskat)abstract
    • Vertebrate locomotion is orchestrated by spinal interneurons making up a central pattern generator. Proper coordination of activity, both within and between segments, is required to generate the desired locomotor output. This coordination is altered during acceleration to ensure the correct recruitment of muscles for the chosen speed. The transcription factor Dmrt3 has been proposed to shape the patterned output at different gaits in horses and mice. Here, we characterized dmrt3a mutant zebrafish, which showed a strong, transient, locomotor phenotype in developing larvae. During beat-and-glide swimming, mutant larvae showed fewer and shorter movements with decreased velocity and acceleration. Developmental compensation likely occurs as the analyzed behaviors did not differ from wild-type at older larval stages. However, analysis of maximum swim speed in juveniles suggests that some defects persist within the mature locomotor network of dmrt3a mutants. Our results reveal the pivotal role Dmrt3 neurons play in shaping the patterned output during acceleration in vertebrates.
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4.
  • Guruprasad, Puneeth, et al. (författare)
  • Integrated automated particle tracking microfluidic enables high-throughput cell deformability cytometry for red cell disorders
  • 2019
  • Ingår i: American Journal of Hematology. - : Wiley-Blackwell. - 0361-8609 .- 1096-8652. ; 94:2, s. 189-199
  • Tidskriftsartikel (refereegranskat)abstract
    • Investigating individual red blood cells (RBCs) is critical to understanding hematologic diseases, as pathology often originates at the single-cell level. Many RBC disorders manifest in altered biophysical properties, such as deformability of RBCs. Due to limitations in current biophysical assays, there exists a need for high-throughput analysis of RBC deformability with single-cell resolution. To that end, we present a method that pairs a simple in vitro artificial microvasculature network system with an innovative MATLAB-based automated particle tracking program, allowing for high-throughput, single-cell deformability index (sDI) measurements of entire RBC populations. We apply our technology to quantify the sDI of RBCs from healthy volunteers, Sickle cell disease (SCD) patients, a transfusion-dependent beta thalassemia major patient, and in stored packed RBCs (pRBCs) that undergo storage lesion over 4 weeks. Moreover, our system can also measure cell size for each RBC, thereby enabling 2D analysis of cell deformability vs cell size with single cell resolution akin to flow cytometry. Our results demonstrate the clear existence of distinct biophysical RBC subpopulations with high interpatient variability in SCD as indicated by large magnitude skewness and kurtosis values of distribution, the "shifting" of sDI vs RBC size curves over transfusion cycles in beta thalassemia, and the appearance of low sDI RBC subpopulations within 4 days of pRBC storage. Overall, our system offers an inexpensive, convenient, and high-throughput method to gauge single RBC deformability and size for any RBC population and has the potential to aid in disease monitoring and transfusion guidelines for various RBC disorders.
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5.
  • Habicher, Judith, et al. (författare)
  • Chondroitin/dermatan sulfate glycosyltransferase genes are essential for craniofacial development
  • 2022
  • Ingår i: PLOS Genetics. - : Public Library of Science (PLoS). - 1553-7390 .- 1553-7404. ; 18:2
  • Tidskriftsartikel (refereegranskat)abstract
    • Chondroitin/dermatan sulfate (CS/DS) proteoglycans are indispensable for animal development and homeostasis but the large number of enzymes involved in their biosynthesis have made CS/DS function a challenging problem to study genetically. In our study, we generated loss-of-function alleles in zebrafish genes encoding CS/DS biosynthetic enzymes and characterized the effect on development in single and double mutants. Homozygous mutants in chsy1, csgalnact1a, csgalnat2, chpfa, ust and chst7, respectively, develop to adults. However, csgalnact1a-/- fish develop distinct craniofacial defects while the chsy1-/- skeletal phenotype is milder and the remaining mutants display no gross morphological abnormalities. These results suggest a high redundancy for the CS/DS biosynthetic enzymes and to further reduce CS/DS biosynthesis we combined mutant alleles. The craniofacial phenotype is further enhanced in csgalnact1a-/-;chsy1-/- adults and csgalnact1a-/-;csgalnact2-/- larvae. While csgalnact1a-/-;csgalnact2-/- was the most affected allele combination in our study, CS/DS is still not completely abolished. Transcriptome analysis of chsy1-/-, csgalnact1a-/- and csgalnact1a-/-;csgalnact2-/- larvae revealed that the expression had changed in a similar way in the three mutant lines but no differential expression was found in any of fifty GAG biosynthesis enzymes identified. Thus, zebrafish larvae do not increase transcription of GAG biosynthesis genes as a consequence of decreased CS/DS biosynthesis. The new zebrafish lines develop phenotypes similar to clinical characteristics of several human congenital disorders making the mutants potentially useful to study disease mechanisms and treatment.
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6.
  • Hanqing, Zhang, et al. (författare)
  • A fast and robust circle detection method using isosceles triangles sampling
  • 2016
  • Ingår i: Pattern Recognition. - : Elsevier. - 0031-3203 .- 1873-5142. ; 54, s. 218-228
  • Tidskriftsartikel (refereegranskat)abstract
    • Circle detection using randomized sampling has been developed in recent years to reduce computational intensity. However, randomized sampling is sensitive to noise that can lead to reduced accuracy and false-positive candidates. To improve on the robustness of randomized circle detection under noisy conditions this paper presents a new methodology for circle detection based upon randomized isosceles triangles sampling. It is shown that the geometrical property of isosceles triangles provides a robust criterion to find relevant edge pixels which, in turn, offers an efficient means to estimate the centers and radii of circles. For best efficiency, the estimated results given by the sampling from individual connected components of the edge map were analyzed using a simple clustering approach. To further improve on the accuracy we applied a two-step refinement process using chords and linear error compensation with gradient information of the edge pixels. Extensive experiments using both synthetic and real images have been performed. The results are compared to leading state-of-the-art algorithms and it is shown that the proposed methodology has a number of advantages: it is efficient in finding circles with a low number of iterations, it has high rejection rate of false-positive circle candidates, and it has high robustness against noise. All this makes it adaptive and useful in many vision applications.
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7.
  • Leyhr, Jake, et al. (författare)
  • A novel cis-regulatory element drives early expression of Nkx3.2 in the gnathostome primary jaw joint
  • 2022
  • Ingår i: eLIFE. - : eLife Sciences Publications Ltd. - 2050-084X. ; 11
  • Tidskriftsartikel (refereegranskat)abstract
    • The acquisition of movable jaws was a major event during vertebrate evolution. The role of NK3 homeobox 2 (Nkx3.2) transcription factor in patterning the primary jaw joint of gnathostomes (jawed vertebrates) is well known, however knowledge about its regulatory mechanism is lacking. In this study, we report a proximal enhancer element of Nkx3.2 that is deeply conserved in most gnathostomes but undetectable in the jawless hagfish and lamprey. This enhancer is active in the developing jaw joint region of the zebrafish Danio rerio, and was thus designated as jaw joint regulatory sequence 1 (JRS1). We further show that JRS1 enhancer sequences from a range of gnathostome species, including a chondrichthyan and mammals, have the same activity in the jaw joint as the native zebrafish enhancer, indicating a high degree of functional conservation despite the divergence of cartilaginous and bony fish lineages or the transition of the primary jaw joint into the middle ear of mammals. Finally, we show that deletion of JRS1 from the zebrafish genome using CRISPR/Cas9 results in a significant reduction of early gene expression of nkx3.2 and leads to a transient jaw joint deformation and partial fusion. Emergence of this Nkx3.2 enhancer in early gnathostomes may have contributed to the origin and shaping of the articulating surfaces of vertebrate jaws.
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