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 *

231 related articles for article (PubMed ID: 22607156)

  • 1. Exome sequencing generates high quality data in non-target regions.
    Guo Y; Long J; He J; Li CI; Cai Q; Shu XO; Zheng W; Li C
    BMC Genomics; 2012 May; 13():194. PubMed ID: 22607156
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. The effect of strand bias in Illumina short-read sequencing data.
    Guo Y; Li J; Li CI; Long J; Samuels DC; Shyr Y
    BMC Genomics; 2012 Nov; 13():666. PubMed ID: 23176052
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison and evaluation of two exome capture kits and sequencing platforms for variant calling.
    Zhang G; Wang J; Yang J; Li W; Deng Y; Li J; Huang J; Hu S; Zhang B
    BMC Genomics; 2015 Aug; 16(1):581. PubMed ID: 26242175
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comprehensive comparison of three commercial human whole-exome capture platforms.
    Asan ; Xu Y; Jiang H; Tyler-Smith C; Xue Y; Jiang T; Wang J; Wu M; Liu X; Tian G; Wang J; Wang J; Yang H; Zhang X
    Genome Biol; 2011 Sep; 12(9):R95. PubMed ID: 21955857
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Performance of microarray and liquid based capture methods for target enrichment for massively parallel sequencing and SNP discovery.
    Kiialainen A; Karlberg O; Ahlford A; Sigurdsson S; Lindblad-Toh K; Syvänen AC
    PLoS One; 2011 Feb; 6(2):e16486. PubMed ID: 21347407
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome genotyping, linkage disequilibrium and population structure in loblolly pine (Pinus taeda L.).
    Lu M; Krutovsky KV; Nelson CD; Koralewski TE; Byram TD; Loopstra CA
    BMC Genomics; 2016 Sep; 17(1):730. PubMed ID: 27624183
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparison of SureSelect and Nextera Exome Capture Performance in Single-Cell Sequencing.
    Huss WJ; Hu Q; Glenn ST; Gangavarapu KJ; Wang J; Luce JD; Quinn PK; Brese EA; Zhan F; Conroy JM; Paragh G; Foster BA; Morrison CD; Liu S; Wei L
    Hum Hered; 2018; 83(3):153-162. PubMed ID: 30669152
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Improving mapping and SNP-calling performance in multiplexed targeted next-generation sequencing.
    Elsharawy A; Forster M; Schracke N; Keller A; Thomsen I; Petersen BS; Stade B; Stähler P; Schreiber S; Rosenstiel P; Franke A
    BMC Genomics; 2012 Aug; 13():417. PubMed ID: 22913592
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Performance comparison of exome DNA sequencing technologies.
    Clark MJ; Chen R; Lam HY; Karczewski KJ; Chen R; Euskirchen G; Butte AJ; Snyder M
    Nat Biotechnol; 2011 Sep; 29(10):908-14. PubMed ID: 21947028
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Finding the lost treasures in exome sequencing data.
    Samuels DC; Han L; Li J; Quanghu S; Clark TA; Shyr Y; Guo Y
    Trends Genet; 2013 Oct; 29(10):593-9. PubMed ID: 23972387
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Ionizing Radiation Alters the Transition/Transversion Ratio in the Exome of Human Gingiva Fibroblasts.
    Nath N; Hagenau L; Weiss S; Tzvetkova A; Jensen LR; Kaderali L; Port M; Scherthan H; Kuss AW
    Health Phys; 2020 Jul; 119(1):109-117. PubMed ID: 32483046
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sequence variants from whole genome sequencing a large group of Icelanders.
    Gudbjartsson DF; Sulem P; Helgason H; Gylfason A; Gudjonsson SA; Zink F; Oddson A; Magnusson G; Halldorsson BV; Hjartarson E; Sigurdsson GT; Kong A; Helgason A; Masson G; Magnusson OT; Thorsteinsdottir U; Stefansson K
    Sci Data; 2015; 2():150011. PubMed ID: 25977816
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted high throughput sequencing of a cancer-related exome subset by specific sequence capture with a fully automated microarray platform.
    Summerer D; Schracke N; Wu H; Cheng Y; Bau S; Stähler CF; Stähler PF; Beier M
    Genomics; 2010 Apr; 95(4):241-6. PubMed ID: 20138981
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.
    Kim YJ; Lee J; Kim BJ; ; Park T
    BMC Genomics; 2015 Dec; 16():1109. PubMed ID: 26715385
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mitochondria sequence mapping strategies and practicability of mitochondria variant detection from exome and RNA sequencing data.
    Zhang P; Samuels DC; Lehmann B; Stricker T; Pietenpol J; Shyr Y; Guo Y
    Brief Bioinform; 2016 Mar; 17(2):224-32. PubMed ID: 26249222
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population.
    Motoike IN; Matsumoto M; Danjoh I; Katsuoka F; Kojima K; Nariai N; Sato Y; Yamaguchi-Kabata Y; Ito S; Kudo H; Nishijima I; Nishikawa S; Pan X; Saito R; Saito S; Saito T; Shirota M; Tsuda K; Yokozawa J; Igarashi K; Minegishi N; Tanabe O; Fuse N; Nagasaki M; Kinoshita K; Yasuda J; Yamamoto M
    BMC Genomics; 2014 Aug; 15(1):673. PubMed ID: 25109789
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Performance comparison of four commercial human whole-exome capture platforms.
    Shigemizu D; Momozawa Y; Abe T; Morizono T; Boroevich KA; Takata S; Ashikawa K; Kubo M; Tsunoda T
    Sci Rep; 2015 Aug; 5():12742. PubMed ID: 26235669
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.