BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 27098910)

  • 1. Efficient Genome-Wide Sequencing and Low-Coverage Pedigree Analysis from Noninvasively Collected Samples.
    Snyder-Mackler N; Majoros WH; Yuan ML; Shaver AO; Gordon JB; Kopp GH; Schlebusch SA; Wall JD; Alberts SC; Mukherjee S; Zhou X; Tung J
    Genetics; 2016 Jun; 203(2):699-714. PubMed ID: 27098910
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome characterization in pedigreed non-human primates using genotyping-by-sequencing (GBS) and imputation.
    Bimber BN; Raboin MJ; Letaw J; Nevonen KA; Spindel JE; McCouch SR; Cervera-Juanes R; Spindel E; Carbone L; Ferguson B; Vinson A
    BMC Genomics; 2016 Aug; 17(1):676. PubMed ID: 27558348
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Methylation-based enrichment facilitates low-cost, noninvasive genomic scale sequencing of populations from feces.
    Chiou KL; Bergey CM
    Sci Rep; 2018 Jan; 8(1):1975. PubMed ID: 29386638
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Skim-Based Genotyping by Sequencing Using a Double Haploid Population to Call SNPs, Infer Gene Conversions, and Improve Genome Assemblies.
    Bayer PE
    Methods Mol Biol; 2016; 1374():285-92. PubMed ID: 26519413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Improved ancestry estimation for both genotyping and sequencing data using projection procrustes analysis and genotype imputation.
    Wang C; Zhan X; Liang L; Abecasis GR; Lin X
    Am J Hum Genet; 2015 Jun; 96(6):926-37. PubMed ID: 26027497
    [TBL] [Abstract][Full Text] [Related]  

  • 6. mInDel: a high-throughput and efficient pipeline for genome-wide InDel marker development.
    Lv Y; Liu Y; Zhao H
    BMC Genomics; 2016 Apr; 17():290. PubMed ID: 27079510
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low-depth genotyping-by-sequencing (GBS) in a bovine population: strategies to maximize the selection of high quality genotypes and the accuracy of imputation.
    Brouard JS; Boyle B; Ibeagha-Awemu EM; Bissonnette N
    BMC Genet; 2017 Apr; 18(1):32. PubMed ID: 28381212
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Generating RNA Baits for Capture-Based Enrichment.
    Snyder-Mackler N; Voyles T; Tung J
    Methods Mol Biol; 2019; 1963():107-120. PubMed ID: 30875049
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A highly robust and optimized sequence-based approach for genetic polymorphism discovery and genotyping in large plant populations.
    Jiang N; Zhang F; Wu J; Chen Y; Hu X; Fang O; Leach LJ; Wang D; Luo Z
    Theor Appl Genet; 2016 Sep; 129(9):1739-57. PubMed ID: 27316437
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Assessing the enrichment performance in targeted resequencing experiments.
    Frommolt P; Abdallah AT; Altmüller J; Motameny S; Thiele H; Becker C; Stemshorn K; Fischer M; Freilinger T; Nürnberg P
    Hum Mutat; 2012 Apr; 33(4):635-41. PubMed ID: 22290614
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deriving genotypes from RAD-seq short-read data using Stacks.
    Rochette NC; Catchen JM
    Nat Protoc; 2017 Dec; 12(12):2640-2659. PubMed ID: 29189774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Can whole-exome sequencing data be used for linkage analysis?
    Gazal S; Gosset S; Verdura E; Bergametti F; Guey S; Babron MC; Tournier-Lasserve E
    Eur J Hum Genet; 2016 Apr; 24(4):581-6. PubMed ID: 26173971
    [TBL] [Abstract][Full Text] [Related]  

  • 14. megasat: automated inference of microsatellite genotypes from sequence data.
    Zhan L; Paterson IG; Fraser BA; Watson B; Bradbury IR; Nadukkalam Ravindran P; Reznick D; Beiko RG; Bentzen P
    Mol Ecol Resour; 2017 Mar; 17(2):247-256. PubMed ID: 27333119
    [TBL] [Abstract][Full Text] [Related]  

  • 15. LINKPHASE3: an improved pedigree-based phasing algorithm robust to genotyping and map errors.
    Druet T; Georges M
    Bioinformatics; 2015 May; 31(10):1677-9. PubMed ID: 25573918
    [TBL] [Abstract][Full Text] [Related]  

  • 16. swinger: a user-friendly computer program to establish captive breeding groups that minimize relatedness without pedigree information.
    Sandoval-Castillo J; Attard CR; Marri S; Brauer CJ; Möller LM; Beheregaray LB
    Mol Ecol Resour; 2017 Mar; 17(2):278-287. PubMed ID: 27754599
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™.
    Eduardoff M; Santos C; de la Puente M; Gross TE; Fondevila M; Strobl C; Sobrino B; Ballard D; Schneider PM; Carracedo Á; Lareu MV; Parson W; Phillips C
    Forensic Sci Int Genet; 2015 Jul; 17():110-121. PubMed ID: 25955683
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GenomeLaser: fast and accurate haplotyping from pedigree genotypes.
    Li W; Fu G; Rao W; Xu W; Ma L; Guo S; Song Q
    Bioinformatics; 2015 Dec; 31(24):3984-7. PubMed ID: 26286810
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotyping methodologies.
    Bevan S; Houlston RS
    Mol Biotechnol; 2001 Jan; 17(1):83-9. PubMed ID: 11280934
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Conservation of human chromosome 18 in baboons (Papio hamadryas): a linkage map of eight human microsatellites.
    Perelygin AA; Kammerer CM; Stowell NC; Rogers J
    Cytogenet Cell Genet; 1996; 75(4):207-9. PubMed ID: 9067425
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.