BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 29423797)

  • 1. Whole Genome Library Construction for Next Generation Sequencing.
    Keats JJ; Cuyugan L; Adkins J; Liang WS
    Methods Mol Biol; 2018; 1706():151-161. PubMed ID: 29423797
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long insert whole genome sequencing for copy number variant and translocation detection.
    Liang WS; Aldrich J; Tembe W; Kurdoglu A; Cherni I; Phillips L; Reiman R; Baker A; Weiss GJ; Carpten JD; Craig DW
    Nucleic Acids Res; 2014 Jan; 42(2):e8. PubMed ID: 24071583
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole Exome Library Construction for Next Generation Sequencing.
    Liang WS; Stephenson K; Adkins J; Christofferson A; Helland A; Cuyugan L; Keats JJ
    Methods Mol Biol; 2018; 1706():163-174. PubMed ID: 29423798
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A performance evaluation of Nextera XT and KAPA HyperPlus for rapid Illumina library preparation of long-range mitogenome amplicons.
    Ring JD; Sturk-Andreaggi K; Peck MA; Marshall C
    Forensic Sci Int Genet; 2017 Jul; 29():174-180. PubMed ID: 28448897
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Next Generation Sequencing of Prenatal Structural Chromosomal Rearrangements Using Large-Insert Libraries.
    Currall BB; Antolik CW; Collins RL; Talkowski ME
    Methods Mol Biol; 2019; 1885():251-265. PubMed ID: 30506203
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Library preparation methodology can influence genomic and functional predictions in human microbiome research.
    Jones MB; Highlander SK; Anderson EL; Li W; Dayrit M; Klitgord N; Fabani MM; Seguritan V; Green J; Pride DT; Yooseph S; Biggs W; Nelson KE; Venter JC
    Proc Natl Acad Sci U S A; 2015 Nov; 112(45):14024-9. PubMed ID: 26512100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantification of Aneuploidy in Mammalian Systems.
    van den Bos H; Bakker B; Taudt A; Guryev V; Colomé-Tatché M; Lansdorp PM; Foijer F; Spierings DCJ
    Methods Mol Biol; 2019; 1896():159-190. PubMed ID: 30474848
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New library construction method for single-cell genomes.
    Xi L; Belyaev A; Spurgeon S; Wang X; Gong H; Aboukhalil R; Fekete R
    PLoS One; 2017; 12(7):e0181163. PubMed ID: 28723968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
    Hollegaard MV; Grauholm J; Nielsen R; Grove J; Mandrup S; Hougaard DM
    Mol Genet Metab; 2013; 110(1-2):65-72. PubMed ID: 23830478
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Preparation of fragment libraries for next-generation sequencing on the applied biosystems SOLiD platform.
    Yegnasubramanian S
    Methods Enzymol; 2013; 529():185-200. PubMed ID: 24011046
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten.
    Nair SS; Luu PL; Qu W; Maddugoda M; Huschtscha L; Reddel R; Chenevix-Trench G; Toso M; Kench JG; Horvath LG; Hayes VM; Stricker PD; Hughes TP; White DL; Rasko JEJ; Wong JJ; Clark SJ
    Epigenetics Chromatin; 2018 May; 11(1):24. PubMed ID: 29807544
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations.
    Wang M; Beck CR; English AC; Meng Q; Buhay C; Han Y; Doddapaneni HV; Yu F; Boerwinkle E; Lupski JR; Muzny DM; Gibbs RA
    BMC Genomics; 2015 Mar; 16(1):214. PubMed ID: 25887218
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Next-generation sequencing library construction on a surface.
    Feng K; Costa J; Edwards JS
    BMC Genomics; 2018 May; 19(1):416. PubMed ID: 29848309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multi-laboratory evaluation of the Illumina iSeq platform for whole genome sequencing of
    Mitchell PK; Wang L; Stanhope BJ; Cronk BD; Anderson R; Mohan S; Zhou L; Sanchez S; Bartlett P; Maddox C; DeShambo V; Mani R; Hengesbach LM; Gresch S; Wright K; Mor S; Zhang S; Shen Z; Yan L; Mackey R; Franklin-Guild R; Zhang Y; Prarat M; Shiplett K; Ramachandran A; Narayanan S; Sanders J; Hunkapiller AA; Lahmers K; Carbonello AA; Aulik N; Lim A; Cooper J; Jones A; Guag J; Nemser SM; Tyson GH; Timme R; Strain E; Reimschuessel R; Ceric O; Goodman LB
    Microb Genom; 2022 Feb; 8(2):. PubMed ID: 35113783
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of a high-throughput, cost-effective Illumina library preparation kit.
    Tvedte ES; Michalski J; Cheng S; Patkus RS; Tallon LJ; Sadzewicz L; Bruno VM; Silva JC; Rasko DA; Dunning Hotopp JC
    Sci Rep; 2021 Aug; 11(1):15925. PubMed ID: 34354114
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
    Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
    Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Efficient and unique cobarcoding of second-generation sequencing reads from long DNA molecules enabling cost-effective and accurate sequencing, haplotyping, and de novo assembly.
    Wang O; Chin R; Cheng X; Wu MKY; Mao Q; Tang J; Sun Y; Anderson E; Lam HK; Chen D; Zhou Y; Wang L; Fan F; Zou Y; Xie Y; Zhang RY; Drmanac S; Nguyen D; Xu C; Villarosa C; Gablenz S; Barua N; Nguyen S; Tian W; Liu JS; Wang J; Liu X; Qi X; Chen A; Wang H; Dong Y; Zhang W; Alexeev A; Yang H; Wang J; Kristiansen K; Xu X; Drmanac R; Peters BA
    Genome Res; 2019 May; 29(5):798-808. PubMed ID: 30940689
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Optimized Illumina PCR-free library preparation for bacterial whole genome sequencing and analysis of factors influencing de novo assembly.
    Huptas C; Scherer S; Wenning M
    BMC Res Notes; 2016 May; 9():269. PubMed ID: 27176120
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Copy number alterations detected by whole-exome and whole-genome sequencing of esophageal adenocarcinoma.
    Wang X; Li X; Cheng Y; Sun X; Sun X; Self S; Kooperberg C; Dai JY
    Hum Genomics; 2015 Sep; 9(1):22. PubMed ID: 26374103
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Optimization and cost-saving in tagmentation-based mate-pair library preparation and sequencing.
    Tatsumi K; Nishimura O; Itomi K; Tanegashima C; Kuraku S
    Biotechniques; 2015 May; 58(5):253-7. PubMed ID: 25967904
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.