BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

170 related articles for article (PubMed ID: 24507442)

  • 1. SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing.
    Quail MA; Smith M; Jackson D; Leonard S; Skelly T; Swerdlow HP; Gu Y; Ellis P
    BMC Genomics; 2014 Feb; 15(1):110. PubMed ID: 24507442
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enhancing the detection of barcoded reads in high throughput DNA sequencing data by controlling the false discovery rate.
    Buschmann T; Zhang R; Brash DE; Bystrykh LV
    BMC Bioinformatics; 2014 Aug; 15(1):264. PubMed ID: 25099007
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sample Tracking Using Unique Sequence Controls.
    Moore RA; Zeng T; Docking TR; Bosdet I; Butterfield YS; Munro S; Li I; Swanson L; Starks ER; Tse K; Mungall AJ; Holt RA; Karsan A
    J Mol Diagn; 2020 Feb; 22(2):141-146. PubMed ID: 31837431
    [TBL] [Abstract][Full Text] [Related]  

  • 4. RNA Fragmentation and Sequencing (RF-Seq): Cost-Effective, Time-Efficient, and High-Throughput 3' mRNA Sequencing Library Construction in a Single Tube.
    Veeranagouda Y; Remaury A; Guillemot JC; Didier M
    Curr Protoc Mol Biol; 2019 Dec; 129(1):e109. PubMed ID: 31763778
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Quantitative bias in Illumina TruSeq and a novel post amplification barcoding strategy for multiplexed DNA and small RNA deep sequencing.
    Van Nieuwerburgh F; Soetaert S; Podshivalova K; Ay-Lin Wang E; Schaffer L; Deforce D; Salomon DR; Head SR; Ordoukhanian P
    PLoS One; 2011; 6(10):e26969. PubMed ID: 22046424
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hackflex: low-cost, high-throughput, Illumina Nextera Flex library construction.
    Gaio D; Anantanawat K; To J; Liu M; Monahan L; Darling AE
    Microb Genom; 2022 Jan; 8(1):. PubMed ID: 35014949
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Barcode-free next-generation sequencing error validation for ultra-rare variant detection.
    Yeom H; Lee Y; Ryu T; Noh J; Lee AC; Lee HB; Kang E; Song SW; Kwon S
    Nat Commun; 2019 Feb; 10(1):977. PubMed ID: 30816127
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impact of next-generation sequencing error on analysis of barcoded plasmid libraries of known complexity and sequence.
    Deakin CT; Deakin JJ; Ginn SL; Young P; Humphreys D; Suter CM; Alexander IE; Hallwirth CV
    Nucleic Acids Res; 2014; 42(16):e129. PubMed ID: 25013183
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Massively parallel sequencing of the entire control region and targeted coding region SNPs of degraded mtDNA using a simplified library preparation method.
    Lee EY; Lee HY; Oh SY; Jung SE; Yang IS; Lee YH; Yang WI; Shin KJ
    Forensic Sci Int Genet; 2016 May; 22():37-43. PubMed ID: 26844917
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Insertion and deletion correcting DNA barcodes based on watermarks.
    Kracht D; Schober S
    BMC Bioinformatics; 2015 Feb; 16():50. PubMed ID: 25887410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Embryo tracking system for high-throughput sequencing-based preimplantation genetic testing.
    van Dijk W; Derks K; Drüsedau M; Meekels J; Koeck R; Essers R; Dreesen J; Coonen E; de Die-Smulders C; Stevens SJC; Brunner HG; van den Wijngaard A; Paulussen ADC; Zamani Esteki M
    Hum Reprod; 2022 Oct; 37(11):2700-2708. PubMed ID: 36149256
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pseudo-Sanger sequencing: massively parallel production of long and near error-free reads using NGS technology.
    Ruan J; Jiang L; Chong Z; Gong Q; Li H; Li C; Tao Y; Zheng C; Zhai W; Turissini D; Cannon CH; Lu X; Wu CI
    BMC Genomics; 2013 Oct; 14(1):711. PubMed ID: 24134808
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel ultra high-throughput 16S rRNA gene amplicon sequencing library preparation method for the Illumina HiSeq platform.
    de Muinck EJ; Trosvik P; Gilfillan GD; Hov JR; Sundaram AYM
    Microbiome; 2017 Jul; 5(1):68. PubMed ID: 28683838
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next-generation sequencing of multiple individuals per barcoded library by deconvolution of sequenced amplicons using endonuclease fragment analysis.
    Andersen JD; Pereira V; Pietroni C; Mikkelsen M; Johansen P; Børsting C; Morling N
    Biotechniques; 2014 Aug; 57(2):91-4. PubMed ID: 25109295
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Simple multiplexed PCR-based barcoding of DNA for ultrasensitive mutation detection by next-generation sequencing.
    Ståhlberg A; Krzyzanowski PM; Egyud M; Filges S; Stein L; Godfrey TE
    Nat Protoc; 2017 Apr; 12(4):664-682. PubMed ID: 28253235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Role of Quality Control in Targeted Next-generation Sequencing Library Preparation.
    Nietsch R; Haas J; Lai A; Oehler D; Mester S; Frese KS; Sedaghat-Hamedani F; Kayvanpour E; Keller A; Meder B
    Genomics Proteomics Bioinformatics; 2016 Aug; 14(4):200-6. PubMed ID: 27475404
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High-specificity detection of rare alleles with Paired-End Low Error Sequencing (PELE-Seq).
    Preston JL; Royall AE; Randel MA; Sikkink KL; Phillips PC; Johnson EA
    BMC Genomics; 2016 Jun; 17():464. PubMed ID: 27301885
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Performance evaluation of a mitogenome capture and Illumina sequencing protocol using non-probative, case-type skeletal samples: Implications for the use of a positive control in a next-generation sequencing procedure.
    Marshall C; Sturk-Andreaggi K; Daniels-Higginbotham J; Oliver RS; Barritt-Ross S; McMahon TP
    Forensic Sci Int Genet; 2017 Nov; 31():198-206. PubMed ID: 29101892
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sample tracking in microbiome community profiling assays using synthetic 16S rRNA gene spike-in controls.
    Tourlousse DM; Ohashi A; Sekiguchi Y
    Sci Rep; 2018 Jun; 8(1):9095. PubMed ID: 29904073
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.