PubMed Clinical Queries for "Whole genome sequencing"

PubMed Clinical Queries



From PubMed Clinical Queries

PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas

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• Search PubMed Clinical Queries for "Whole genome sequencing" 

Results: 5 of 1286

• Impact of Amoxicillin-Clavulanate followed by Autologous Fecal Microbiota Transplantation on Fecal Microbiome Structure and Metabolic Potential.
  Bulow C, Langdon A, Hink T, Wallace M, Reske KA, Patel S, Sun X, Seiler S, Jones S, Kwon JH, et al.mSphere. 2018 Nov 21; 3(6). Epub 2018 Nov 21.
• Iatrogenic endometriosis harbors somatic cancer-driver mutations.
  Lac V, Verhoef L, Aguirre-Hernandez R, Nazeran TM, Tessier-Cloutier B, Praetorius T, Orr NL, Noga H, Lum A, Khattra J, et al.Hum Reprod. 2018 Nov 14; . Epub 2018 Nov 14.
• Characterization of Duck (<i>Anas platyrhynchos</i>) Short Tandem Repeat Variation by Population-Scale Genome Resequencing.
  Fan W, Xu L, Cheng H, Li M, Liu H, Jiang Y, Guo Y, Zhou Z, Hou S.Front Genet. 2018; 9:520. Epub 2018 Oct 30.
• Bronchiectasis.
  McShane PJ, Tino G.Chest. 2018 Nov 4; . Epub 2018 Nov 4.
• A non-randomized procedure for large-scale heterogeneous multiple discrete testing based on randomized tests.
  Dai X, Lin N, Li D, Wang T.Biometrics. 2018 Nov 2; . Epub 2018 Nov 2.

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This column displays citations filtered to a specific clinical study category and scope. These search filters were developed by Haynes RB et al. See more filter information.

Systematic Reviews

Results: 5 of 167

• VFDB 2019: a comparative pathogenomic platform with an interactive web interface.
  Liu B, Zheng D, Jin Q, Chen L, Yang J.Nucleic Acids Res. 2018 Nov 5; . Epub 2018 Nov 5.
• A stroke gene panel for whole-exome sequencing.
  Ilinca A, Samuelsson S, Piccinelli P, Soller M, Kristoffersson U, Lindgren AG.Eur J Hum Genet. 2018 Oct 24; . Epub 2018 Oct 24.
• Diversity of vaginal microbiota in sub-Saharan Africa and its effects on HIV transmission and prevention.
  Bayigga L, Kateete DP, Anderson DJ, Sekikubo M, Nakanjako D.Am J Obstet Gynecol. 2018 Oct 12; . Epub 2018 Oct 12.
• 'How to do it' - a molecular investigation of a hospital outbreak.
  Nutman A, Marchaim D.Clin Microbiol Infect. 2018 Oct 1; . Epub 2018 Oct 1.
• Size Matters: Dissecting Key Parameters for Panel-Based Tumor Mutational Burden (TMB) Analysis.
  Buchhalter I, Rempel E, Endris V, Allgäuer M, Neumann O, Volckmar AL, Kirchner M, Leichsenring J, Lier A, von Winterfeld M, et al.Int J Cancer. 2018 Sep 21; . Epub 2018 Sep 21.

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This column displays citations for systematic reviews, meta-analyses, reviews of clinical trials, evidence-based medicine, consensus development conferences, and guidelines. See filter information or additional related sources.

Medical Genetics

Topic:AllDiagnosisDifferential DiagnosisClinical DescriptionManagementGenetic CounselingMolecular GeneticsGenetic Testing

Results: 5 of 15060

• Research Progress on InDel Genetic Marker in Forensic Science.
  Sheng X, Bao Y, Zhang JS, Li M, Li YN, Xu QN, Zhang SH, Li CT.Fa Yi Xue Za Zhi. 2018 Aug; 34(4):420-427. Epub 2018 Aug 25.
• <i>SEC31A</i> mutation affects ER homeostasis, causing neurological syndrome.
  Halperin D, Kadir R, Perez Y, Drabkin M, Yogev Y, Wormser O, Berman EM, Eremenko E, Rotblat B, Shorer Z, et al.J Med Genet. 2018 Nov 21; . Epub 2018 Nov 21.
• Chromosome level high-density integrated genetic maps improve the Pyrus bretschneideri 'DangshanSuli' v1.0 genome.
  Xue H, Wang S, Yao JL, Deng CH, Wang L, Su Y, Zhang H, Zhou H, Sun M, Li X, et al.BMC Genomics. 2018 Nov 21; 19(1):833. Epub 2018 Nov 21.
• Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency.
  Vahidnezhad H, Youssefian L, Saeidian AH, Touati A, Pajouhanfar S, Baghdadi T, Shadmehri AA, Giunta C, Kraenzlin M, Syx D, et al.Matrix Biol. 2018 Nov 18; . Epub 2018 Nov 18.
• Japanese patient with Cole-carpenter syndrome with compound heterozygous variants of SEC24D.
  Takeyari S, Kubota T, Miyata K, Yamamoto K, Nakayama H, Yamamoto K, Ohata Y, Kitaoka T, Yanagi K, Kaname T, et al.Am J Med Genet A. 2018 Nov 21; . Epub 2018 Nov 21.

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This column displays citations pertaining to topics in medical genetics. See more filter information.