Search Results - "next generation sequencing"

Comparing metabarcoding and morphological approaches to identify phytoplankton taxa associated with harmful algal blooms by Svetlana Esenkulova, Ben J.G. Sutherland, Amy Tabata, Nicola Haigh, Christopher M. Pearce, Kristina M. Miller

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Optical DNA Mapping of Plasmids Reveals Clonal Spread of Carbapenem-Resistant <i>Klebsiella pneumoniae</i> in a Large Thai Hospital by Sriram KK, Tsegaye Sewunet, Walaiporn Wangchinda, Teerawit Tangkoskul, Visanu Thamlikitkul, Christian G. Giske, Fredrik Westerlund

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Molecular commensalism: how oral corynebacteria and their extracellular membrane vesicles shape microbiome interactions by Jens Kreth, Jens Kreth, Emily Helliwell, Puthayalai Treerat, Puthayalai Treerat, Justin Merritt, Justin Merritt

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A novel PHKA2 mutation in a Chinese child with glycogen storage disease type IXa: a case report and literature review by Junling Fu, Tong Wang, Xinhua Xiao

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Clinical characteristics and mutation Spectrum of NF1 in 12 Chinese families with orbital/periorbital plexiform Neurofibromatosis type 1 by Peiwei Chai, Yingxiu Luo, Chuandi Zhou, Yefei Wang, Xianqun Fan, Renbing Jia

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Establishment of a cell senescence related prognostic model for predicting prognosis in glioblastoma by Hongbin Li, Zhuozhou Wang, Chengde Sun, Shuangjia Li

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Impact of polyols on Oral microbiome of Estonian schoolchildren by Jelena Štšepetova, Jaak Truu, Riina Runnel, Rita Nõmmela, Mare Saag, Jana Olak, Hiie Nõlvak, Jens-Konrad Preem, Kristjan Oopkaup, Kaarel Krjutškov, Eino Honkala, Sisko Honkala, Kauko Mäkinen, Pirkko-Liisa Mäkinen, Tero Vahlberg, Joan Vermeiren, Douwina Bosscher, Peter de Cock, Reet Mändar

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Biochemical, Molecular, and Clinical Characterization of Patients With Primary Carnitine Deficiency via Large-Scale Newborn Screening in Xuzhou Area by Wei Zhou, Huizhong Li, Ting Huang, Yan Zhang, Chuanxia Wang, Maosheng Gu

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Genomic profiling toward precision medicine in non-small cell lung cancer: getting beyond EGFR by Richer AL, Friel JM, Carson VM, Inge LJ, Whitsett TG

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Successful treatment of diffuse alveolar hemorrhage secondary to Mycoplasma pneumoniae complicated with hemophagocytic lymphohistiocytosis in children: a case report and non-system... by Min Yang, Min Yang, Min Yang, Zhong-Qiang Liu, Zhong-Qiang Liu, Zhong-Qiang Liu, Yang Wang, Yang Wang, Yang Wang, Li-Li Luo, Li-Li Luo, Li-Li Luo, Li-Na Qiao, Li-Na Qiao, Li-Na Qiao

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Intraductal oncocytic papillary neoplasm arising in Peutz-Jeghers Syndrome bile duct: a unique case report by Qingyue Liu, Zhiyu Wang, Chaoran Yu, Jianping Zhu, Chengli Liu, Xiangsheng Li, Li Ren, Teng Li

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Correlation of plasma cell assessment by phenotypic methods and molecular profiles by NGS in patients with plasma cell dyscrasias by Ekaterina Rebmann Chigrinova, Naomi A. Porret, Martin Andres, Gertrud Wiedemann, Yara Banz, Myriam Legros, Matthias Pollak, Elisabeth Oppliger Leibundgut, Thomas Pabst, Ulrike Bacher

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Preimplantation genetic testing for aneuploidy in patients of different age: a systematic review and meta-analysis by Leila Adamyan, Laura Pivazyan, Lilia Obosyan, Ekaterina Krylova, Sapiyat Isaeva

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Phenotypic variability in a child with Felty's syndrome: a case report by Guo-min Li, Hai-mei Liu, Wan-zhen Guan, Yi-fan Li, Hong Xu, Li Sun

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Epithelioid angiomyolipoma of the liver in a patient with Li-Fraumeni syndrome: a case report  by Yaewon Yang, Jisun Lee, Chang Gok Woo, Ok-Jun Lee, Seung-Myoung Son

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PAnno: A pharmacogenomics annotation tool for clinical genomic testing by Yaqing Liu, Zipeng Lin, Qingwang Chen, Qiaochu Chen, Leqing Sang, Yunjin Wang, Yunjin Wang, Leming Shi, Li Guo, Li Guo, Ying Yu

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Conversion therapy with chemoimmunotherapy induced pCR in a stage IV lung squamous cell carcinoma patient harboring EGFR exon 20 insertion by Mingjin Xu, Xingfa Huo, Chuantao Zhang, Xuchen Zhang, Huiyun Wang, Hongmin Yang, Nan Ge, Yongjie Wang, Helei Hou

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A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report by Cong Zhou, Yuanyuan Xiao, Hanbing Xie, Shanling Liu, Jing Wang

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Malignant Perivascular Epithelioid Cell Tumor (PEComa) of the Uterus as Part of the Hereditary Cancer Syndrome: A Case Diagnosed with Multiple Malignancies by Sultan CALISKAN, Omer Salih AKAR, Seda GUN, Mehmet KEFELI

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Enhancing clinical utility: deep learning-based embryo scoring model for non-invasive aneuploidy prediction by Bing-Xin Ma, Guang-Nian Zhao, Zhi-Fei Yi, Yong-Le Yang, Lei Jin, Bo Huang

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