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7,631 Possible Causes for genomic

  • Influenza

    As a result of this project, the number of complete human H3N2 influenza virus genomes in GenBank has already grown from just seven genomes to over 200.[dx.doi.org] […] haemagglutinin (HA) and neuraminidase (NA) sequencing in an apparent cross-site influenza A(H1N1) outbreak in renal transplant and haemodialysis patients, confirmed with whole genome[ncbi.nlm.nih.gov] Genome Res. 8 , 186–194 (1998) 6 Salzberg, S. L., Church, D., DiCuccio, M., Yaschenko, E. & Ostell, J. The genome Assembly Archive: a new public resource.[dx.doi.org]

  • Acute Gastroenteritis

    KEYWORDS: full genome analysis; human rotavirus A; non-structural genes; structural genes[ncbi.nlm.nih.gov] A whole genome sequencing revealed that all of the viral genome segments were highly similar to those of the Rotarix virus, with the exception of five amino acid mutations[ncbi.nlm.nih.gov] The whole-genome sequence was obtained with the Ion Torrent next-generation sequencing platform.[ncbi.nlm.nih.gov]

  • Urinary Tract Infection

    Here, we used genome-wide expression profiling to map the bladder transcriptome of GBS UTI in mice infected transurethrally with uropathogenic GBS that was cultured from a[ncbi.nlm.nih.gov] […] laboratory features and the microbial metagenome of 121 clean-catch urine samples. 16S rDNA gene signatures were successfully obtained for 116 participants, while whole genome[biorxiv.org] Genes Genomics. 2018 Jun;40(6):625-634. doi: 10.1007/s13258-018-0664-6. Epub 2018 Feb 14.[ncbi.nlm.nih.gov]

  • Viral Lower Respiratory Infection

    Whole genome sequencing will also be needed to obtain a more complete coverage of exonic regions ( 43 ), and to explore noncoding and large-scale structural variation.[pnas.org] Reconstruction of the complete human cytomegalovirus genome in a BAC reveals RL13 to be a potent inhibitor of replication.[ijcancerprevention.com] […] loss-of-function variants (LoFs), we searched for variants that were homozygous in at least one study participant, and with a higher minor allele frequency in our cohort than in the genome[pnas.org]

  • Skin Infection

    The genome of S. aureus PVL-producing strains were sequenced and compared.[ncbi.nlm.nih.gov] The VZV genome has at least 70 known or predicted open reading frames (ORFs), but understanding how these gene products function in virulence is difficult because VZV is a[ncbi.nlm.nih.gov] KEYWORDS: Genome sequence; Migrants; Panton–Valentine leucocidin; ST132; Skin infection; Staphylococcus aureus [Indexed for MEDLINE] Free full text[ncbi.nlm.nih.gov]

  • Sinusitis

    […] methicillin resistance among nosocomial isolates and community-acquired strains outlines molecular detection methods for mainstream diagnostic tests assesses the promise of modern genomics[books.google.com]

  • Streptococcal Infection

    Complete genome sequence showed that SDSE is the closest bacterial species to GAS, with approximately 70% of genome coverage.[ncbi.nlm.nih.gov] As individuals vary greatly in their risk of developing such serious infections, investigating how the genome, the inherited blueprint of our bodies, of these patients differs[clinicaltrials.gov] BACKGROUND: Several genome scans have reported linkage of markers on chromosome 7p with asthma and related phenotypes in different populations. A fine mapping ...[well.ox.ac.uk]

  • Pharyngitis

    Whole genome sequencing combined with mutant construction and improvements in animal models for oropharyngeal infection by GAS may help pave the way for new discoveries.[ncbi.nlm.nih.gov] Association Rheumatic Fever, Endocarditis, and Kawasaki Disease Committee of the Council on Cardiovascular Disease in the Young, the Interdisciplinary Council on Functional Genomics[scielo.br]

  • Acute Bronchitis

    The ongoing GRACE programme (Genomics to Combat Resistance Against Antibiotics in Community‐Acquired Lower Respiratory Tract Infections in Europe, www.grace‐lrti.org ) may[doi.org]

  • Osteoporosis

    More than 80 genes or genetic variants have been implicated in risk of osteoporosis by hypothesis-free genome-wide studies.[ncbi.nlm.nih.gov] […] of genomic regions [ 15 ].[doi.org] Several genes identified in robust genome-wide association studies will be the new cutting edge in genetic studies of osteoporosis.[ncbi.nlm.nih.gov]

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