High-Throughput Nucleotide Sequencing

Displaying 1 - 12 of 12CSV
Allen, B. S., Kidd, M., Sue, P. K., & Filkins, L. M. (2025). A Committee-Based Diagnostic Stewardship Model for Pathogen Metagenomic Sequencing in Children. The Journal of Applied Laboratory Medicine, 10(1), 59–65. https://doi.org/10.1093/jalm/jfae084
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Martin, B. E., Sands, T., Bier, L., Bergner, A., Boehme, A. K., & Lippa, N. (2024). Comparing the frequency of variants of uncertain significance (VUS) between ancestry groups in a paediatric epilepsy cohort. Journal of Medical Genetics, 61(7), 645–651. https://doi.org/10.1136/jmg-2023-109450
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Hernandez-Morato, I., & Kemfack, A. M. (2024). Next-Generation Sequencing Application: A Systematic Approach for High-Quality RNA Isolation from Skeletal Muscles. RNA Amplification and Analysis, 13–24. https://doi.org/10.1007/978-1-0716-3918-4_2
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Bridge, J. A., Halling, K. C., Moncur, J. T., Souers, R. J., Hameed, M. R., Fernandes, H., Roy, A., Surrey, L., Tafe, L. J., Vasalos, P., & Lopez-Terrada, D. H. (2023). RNA Sequencing for Solid Tumor Fusion Gene Detection: Proficiency Testing Practice and Performance Comparison. Archives of Pathology & Laboratory Medicine, 148(5), 538–544. https://doi.org/10.5858/arpa.2023-0047-cp
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Metz, J. B., Hornstein, N. J., Sharma, S. D., Worley, J., Gonzalez, C., & Sims, P. A. (2022). High-throughput translational profiling with riboPLATE-seq. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-09638-3
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Pandit, K., Petrescu, J., Cuevas, M., Stephenson, W., Smibert, P., Phatnani, H., & Maniatis, S. (2022). An open source toolkit for repurposing Illumina sequencing systems as versatile fluidics and imaging platforms. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-08740-w
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Dindhoria, K., Monga, I., & Thind, A. S. (2022). Computational approaches and challenges for identification and annotation of non-coding RNAs using RNA-Seq. Functional & Integrative Genomics, 22(6), 1105–1112. https://doi.org/10.1007/s10142-022-00915-y
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Sheng, J., Hod, E. A., Vlad, G., & Chavez, A. (2022). Quantifying protein abundance on single cells using split-pool sequencing on DNA-barcoded antibodies for diagnostic applications. Scientific Reports, 12(1). https://doi.org/10.1038/s41598-022-04842-7
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Church, A. J., Corson, L. B., Kao, P.-C., Imamovic-Tuco, A., Reidy, D., Doan, D., Kang, W., Pinto, N., Maese, L., Laetsch, T. W., Kim, A., Colace, S. I., Macy, M. E., Applebaum, M. A., Bagatell, R., Sabnis, A. J., Weiser, D. A., Glade-Bender, J. L., Homans, A. C., … Janeway, K. A. (2022). Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer. Nature Medicine, 28(8), 1581–1589. https://doi.org/10.1038/s41591-022-01856-6
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