Results 71 to 80 of about 552,282 (159)

MetaSTAARlite: an all-in-one tool for biobank-scale whole-genome sequencing meta-analysis. [PDF]

Nat Comput Sci
Kumarasinghe Y, Williams J, Yuan Y, Wang W, Dias JA, Zhang H, Li Z, Li X.   +7 more
europepmc   +1 more source

Genomics in Equine MEED: Whole-Genome Sequencing and Target Mutation Identification. [PDF]

Animals (Basel)
Tanner K, Mays M, Nguyen TA, Lugo T.
europepmc   +1 more source

Whole-genome sequencing and annotation of probiotic <i>Bacillus amyloliquefaciens</i> COFCAU_P1. [PDF]

Microbiol Resour Announc
Choudhury TG, Khan MIR, Tripathy PS, Kumar S, Saha RK, Kamilya D.   +5 more
europepmc   +1 more source

«Whole genome sequencing»

Swiss Medical Forum ‒ Schweizerisches Medizin-Forum, 2017
Meinel, Dominik M, Seth-Smith, Helena M.B., Egli, Adrian   +2 more
openaire   +3 more sources

Accelerated long-read variant calling with Clair3 for whole-genome sequencing. [PDF]

Bioinformatics
Zheng Z, He M, Yu X, Li J, Chen L, Wong AOK, Zhang J, Zhou Y, Luo R.   +8 more
europepmc   +1 more source

A Novel Approach to Interrogating Whole Genome Sequencing Data to Optimise Clinical Utility. [PDF]

Mol Genet Genomic Med
Sonner S, McKenna C, Heggarty S, Hamill C, Flanagan C, McKee S, Kerr K, Alhazzaa R, McKnight AJ, Mone F.   +9 more
europepmc   +1 more source

Contrasting Features of Papillary and Chromophobe Renal Cell Carcinoma Revealed by Whole-Genome Sequencing. [PDF]

Mol Cancer Res
Culliford R, Mills C, Chubb D, Kinnersley B, Sud A, Cornish AJ, Browning L, Lawrence SED, Bentham R, Frangou A, Gruber AJ, Litchfield K, Wedge DC, Larkin J, Turajlic S, Houlston RS.   +15 more
europepmc   +1 more source

Clinical utility of 'Shaken' biopsies for whole-genome sequencing. [PDF]

J Clin Pathol
Nelan R, Mijuskovic M, Hughes M, Becq J, Kingsbury Z, Tsogka E, He M, Vucenovic D, Craig C, Elgar G, Levey P, Suaris T, Walsh E, Ross M, Jones JL.   +14 more
europepmc   +1 more source

Case Report: Whole genome sequencing of small cell ovarian carcinomas. [PDF]

Front Oncol
Daoud S, Tinsley E, Treacy A, Miller C, Thompson C, Hennessey BT, Toomey S, Furney SJ.   +7 more
europepmc   +1 more source

A deep intronic IFT172 variant causing pseudoexon inclusion identified by whole-genome sequencing in nephronophthisis. [PDF]

CEN Case Rep
Sy PM, Baba M, Fujiwara K, Yamamura N, Kawato K, Nishi E, Aoyama S, Kimura Y, Inoki Y, Nagano C, Sakakibara N, Horinouchi T, Yamamura T, Ishimori S, Morisada N, Nozu K.   +15 more
europepmc   +1 more source