Showing 101 - 120 results of 14,140 for search '"Whole genome sequencing"', query time: 1.05s Refine Results
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    Whole genome sequencing and rare variant analysis in essential tremor families. by Zagaa Odgerel, Shilpa Sonti, Nora Hernandez, Jemin Park, Ruth Ottman, Elan D Louis, Lorraine N Clark

    Published 2019-01-01
    “…The etiology of ET remains largely unexplained. Whole genome sequencing (WGS) is likely to be of value in understanding a large proportion of ET with Mendelian and complex disease inheritance patterns. …”
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  4. 104

    Whole genome sequencing and prediction of antimicrobial susceptibilities in non-tuberculous mycobacteria by Priya Solanki, Marc Lipman, Marc Lipman, Timothy D. McHugh, Giovanni Satta

    Published 2022-11-01
    “…To benefit from the advantages of whole genome sequencing, further advances in resistance prediction need to take place, as well as there being better information on novel drug mutations and an understanding of the impact of whole genome sequencing on NTM treatment outcomes.…”
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  5. 105

    The "most wanted" taxa from the human microbiome for whole genome sequencing. by Anthony A Fodor, Todd Z DeSantis, Kristine M Wylie, Jonathan H Badger, Yuzhen Ye, Theresa Hepburn, Ping Hu, Erica Sodergren, Konstantinos Liolios, Heather Huot-Creasy, Bruce W Birren, Ashlee M Earl

    Published 2012-01-01
    “…Taken together, these results suggest that it should be possible to perform whole-genome sequencing on a large fraction of the human microbiome, including the 'most wanted', and that these sequences should serve to support microbiome studies across multiple cohorts. …”
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    Identification of genomic variations of Azeri buffaloes using whole genome sequencing by Milad Hosseini, Hossein Moradi shahrbabak, Mohamad Moradi shahrbabak

    Published 2023-11-01
    “…Also, introducing the effects of these variations on different genomic regions of Azeri buffaloes have potential applications in breeding programs.Materials and MethodsIn this study, whole genome sequencing of 5 heads of Azeri buffaloes native to Iran was done by Illumina sequencing platform. …”
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    Homozygous duplication identified by whole genome sequencing causes LRBA deficiency by Daniele Merico, Yehonatan Pasternak, Mehdi Zarrei, Edward J. Higginbotham, Bhooma Thiruvahindrapuram, Ori Scott, Jessica Willett-Pachul, Eyal Grunebaum, Julia Upton, Adelle Atkinson, Vy H. D. Kim, Elbay Aliyev, Khalid Fakhro, Stephen W. Scherer, Chaim M. Roifman

    Published 2021-11-01
    “…Abstract In more than one-third of primary immunodeficiency (PID) patients, extensive genetic analysis including whole-exome sequencing (WES) fails to identify the genetic defect. Whole-genome sequencing (WGS) is able to detect variants missed by other genomics platforms, enabling the molecular diagnosis of otherwise unresolved cases. …”
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    Whole Genome Sequencing-Based Comparison of Food Isolates of Cronobacter sakazakii by Mohamed A. Aly, Mohamed A. Aly, Konrad J. Domig, Wolfgang Kneifel, Erik Reimhult

    Published 2019-07-01
    “…In this context, we present the whole genome sequence (WGS) of two different C. sakazakii isolated from skimmed milk powder (C7) and ready-to-eat salad mix (C8), respectively. …”
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    Mapping the serum proteome to neurological diseases using whole genome sequencing by Grace Png, Andrei Barysenka, Linda Repetto, Pau Navarro, Xia Shen, Maik Pietzner, Eleanor Wheeler, Nicholas J. Wareham, Claudia Langenberg, Emmanouil Tsafantakis, Maria Karaleftheri, George Dedoussis, Anders Mälarstig, James F. Wilson, Arthur Gilly, Eleftheria Zeggini

    Published 2021-12-01
    “…Here, the authors use whole genome sequencing data to describe the genetic architecture of neurologically-relevant serum proteins and establish causal protein-neurological disease relationships.…”
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    Using whole genome sequencing to study American foulbrood epidemiology in honeybees. by Joakim Ågren, Marc Oliver Schäfer, Eva Forsgren

    Published 2017-01-01
    “…However, a more powerful alternative is multi-locus sequence typing (MLST) using whole-genome sequencing (WGS), which allows for high-resolution studies of disease outbreaks. …”
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    Identification of Medium-Sized Copy Number Alterations in Whole-Genome Sequencing by Hatice Gulcin Ozer, Aisulu Usubalieva, Adrienne Dorrance, Ayse Selen Yilmaz, Michael Caligiuri, Guido Marcucci, Kun Huang

    Published 2014-01-01
    “…The genome-wide discoveries such as detection of copy number alterations (CNA) from high-throughput whole-genome sequencing data enabled new developments in personalized medicine. …”
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