These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

343 related articles for article (PubMed ID: 26457193)

  • 21. The First Kazakh Whole Genomes: The First Report of NGS Data.
    Akilzhanova A; Kairov U; Rakhimova S; Molkenov A; Rhie A; Kim JI; Seo JS; Zhumadilov Z
    Cent Asian J Glob Health; 2014; 3(Suppl):146. PubMed ID: 29805883
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Variant calling in low-coverage whole genome sequencing of a Native American population sample.
    Bizon C; Spiegel M; Chasse SA; Gizer IR; Li Y; Malc EP; Mieczkowski PA; Sailsbery JK; Wang X; Ehlers CL; Wilhelmsen KC
    BMC Genomics; 2014 Jan; 15():85. PubMed ID: 24479562
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Revising a personal genome by comparing and combining data from two different sequencing platforms.
    Kim D; Kim WY; Lee SY; Lee SY; Yun H; Shin SY; Lee J; Hong Y; Won Y; Kim SJ; Lee YS; Ahn SM
    PLoS One; 2013; 8(4):e60585. PubMed ID: 23593254
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Performance comparison of whole-genome sequencing platforms.
    Lam HY; Clark MJ; Chen R; Chen R; Natsoulis G; O'Huallachain M; Dewey FE; Habegger L; Ashley EA; Gerstein MB; Butte AJ; Ji HP; Snyder M
    Nat Biotechnol; 2011 Dec; 30(1):78-82. PubMed ID: 22178993
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Analytical validation of whole exome and whole genome sequencing for clinical applications.
    Linderman MD; Brandt T; Edelmann L; Jabado O; Kasai Y; Kornreich R; Mahajan M; Shah H; Kasarskis A; Schadt EE
    BMC Med Genomics; 2014 Apr; 7():20. PubMed ID: 24758382
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comparison of whole-genome (13X) and capture (87X) resequencing methods for SNP and genotype callings.
    Roux PF; Marthey S; Djari A; Moroldo M; Esquerré D; Estellé J; Klopp C; Lagarrigue S; Demeure O
    Anim Genet; 2015 Feb; 46(1):82-6. PubMed ID: 25515399
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Comparison of solution-based exome capture methods for next generation sequencing.
    Sulonen AM; Ellonen P; Almusa H; Lepistö M; Eldfors S; Hannula S; Miettinen T; Tyynismaa H; Salo P; Heckman C; Joensuu H; Raivio T; Suomalainen A; Saarela J
    Genome Biol; 2011 Sep; 12(9):R94. PubMed ID: 21955854
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Performance comparison of NextSeq and Ion Proton platforms for molecular diagnosis of clinical oncology.
    Cao F; Gao L; Wei L; Chen Z; Wang Y; Ran X; Meng X; Tao J
    Tumori; 2017 May; 103(3):223-230. PubMed ID: 28127742
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Double-digest RAD sequencing using Ion Proton semiconductor platform (ddRADseq-ion) with nonmodel organisms.
    Recknagel H; Jacobs A; Herzyk P; Elmer KR
    Mol Ecol Resour; 2015 Nov; 15(6):1316-29. PubMed ID: 25808755
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory.
    Mehrotra M; Duose DY; Singh RR; Barkoh BA; Manekia J; Harmon MA; Patel KP; Routbort MJ; Medeiros LJ; Wistuba II; Luthra R
    PLoS One; 2017; 12(8):e0181968. PubMed ID: 28767674
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing.
    Masset H; Zamani Esteki M; Dimitriadou E; Dreesen J; Debrock S; Derhaag J; Derks K; Destouni A; Drüsedau M; Meekels J; Melotte C; Peeraer K; Tšuiko O; van Uum C; Allemeersch J; Devogelaere B; François KO; Happe S; Lorson D; Richards RL; Theuns J; Brunner H; de Die-Smulders C; Voet T; Paulussen A; Coonen E; Vermeesch JR
    Hum Reprod; 2019 Aug; 34(8):1608-1619. PubMed ID: 31348829
    [TBL] [Abstract][Full Text] [Related]  

  • 33. From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability.
    Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid BM; Bjerin O; Gustavsson P; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
    Genome Med; 2019 Nov; 11(1):68. PubMed ID: 31694722
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Optimization of enzymatic fragmentation is crucial to maximize genome coverage: a comparison of library preparation methods for Illumina sequencing.
    Ribarska T; Bjørnstad PM; Sundaram AYM; Gilfillan GD
    BMC Genomics; 2022 Feb; 23(1):92. PubMed ID: 35105301
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Comparison among three variant callers and assessment of the accuracy of imputation from SNP array data to whole-genome sequence level in chicken.
    Ni G; Strom TM; Pausch H; Reimer C; Preisinger R; Simianer H; Erbe M
    BMC Genomics; 2015 Oct; 16():824. PubMed ID: 26486989
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Variant detection sensitivity and biases in whole genome and exome sequencing.
    Meynert AM; Ansari M; FitzPatrick DR; Taylor MS
    BMC Bioinformatics; 2014 Jul; 15(1):247. PubMed ID: 25038816
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Tool evaluation for the detection of variably sized indels from next generation whole genome and targeted sequencing data.
    Wang N; Lysenkov V; Orte K; Kairisto V; Aakko J; Khan S; Elo LL
    PLoS Comput Biol; 2022 Feb; 18(2):e1009269. PubMed ID: 35176018
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evaluating the Calling Performance of a Rare Disease NGS Panel for Single Nucleotide and Copy Number Variants.
    Cacheiro P; Ordóñez-Ugalde A; Quintáns B; Piñeiro-Hermida S; Amigo J; García-Murias M; Pascual-Pascual SI; Grandas F; Arpa J; Carracedo A; Sobrido MJ
    Mol Diagn Ther; 2017 Jun; 21(3):303-313. PubMed ID: 28290094
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Developing a 670k genotyping array to tag ~2M SNPs across 24 horse breeds.
    Schaefer RJ; Schubert M; Bailey E; Bannasch DL; Barrey E; Bar-Gal GK; Brem G; Brooks SA; Distl O; Fries R; Finno CJ; Gerber V; Haase B; Jagannathan V; Kalbfleisch T; Leeb T; Lindgren G; Lopes MS; Mach N; da Câmara Machado A; MacLeod JN; McCoy A; Metzger J; Penedo C; Polani S; Rieder S; Tammen I; Tetens J; Thaller G; Verini-Supplizi A; Wade CM; Wallner B; Orlando L; Mickelson JR; McCue ME
    BMC Genomics; 2017 Jul; 18(1):565. PubMed ID: 28750625
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies.
    Chat V; Ferguson R; Morales L; Kirchhoff T
    Front Genet; 2021; 12():790445. PubMed ID: 35251117
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.