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 *

133 related articles for article (PubMed ID: 19293142)

  • 21. Accounting for Errors in Low Coverage High-Throughput Sequencing Data When Constructing Genetic Maps Using Biparental Outcrossed Populations.
    Bilton TP; Schofield MR; Black MA; Chagné D; Wilcox PL; Dodds KG
    Genetics; 2018 May; 209(1):65-76. PubMed ID: 29487138
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Accounting for genotype uncertainty in the estimation of allele frequencies in autopolyploids.
    Blischak PD; Kubatko LS; Wolfe AD
    Mol Ecol Resour; 2016 May; 16(3):742-54. PubMed ID: 26607217
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Linkage Disequilibrium Estimation in Low Coverage High-Throughput Sequencing Data.
    Bilton TP; McEwan JC; Clarke SM; Brauning R; van Stijn TC; Rowe SJ; Dodds KG
    Genetics; 2018 Jun; 209(2):389-400. PubMed ID: 29588288
    [TBL] [Abstract][Full Text] [Related]  

  • 24. AKSmooth: enhancing low-coverage bisulfite sequencing data via kernel-based smoothing.
    Chen J; Lutsik P; Akulenko R; Walter J; Helms V
    J Bioinform Comput Biol; 2014 Dec; 12(6):1442005. PubMed ID: 25553811
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evaluation of preprocessing, mapping and postprocessing algorithms for analyzing whole genome bisulfite sequencing data.
    Tsuji J; Weng Z
    Brief Bioinform; 2016 Nov; 17(6):938-952. PubMed ID: 26628557
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A new analysis tool for individual-level allele frequency for genomic studies.
    Yang HC; Lin HC; Huang MC; Li LH; Pan WH; Wu JY; Chen YT
    BMC Genomics; 2010 Jul; 11():415. PubMed ID: 20602748
    [TBL] [Abstract][Full Text] [Related]  

  • 27. PPC: an algorithm for accurate estimation of SNP allele frequencies in small equimolar pools of DNA using data from high density microarrays.
    Brohede J; Dunne R; McKay JD; Hannan GN
    Nucleic Acids Res; 2005 Sep; 33(17):e142. PubMed ID: 16199750
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Increasing the information content of STS-based genome maps: identifying polymorphisms in mapped STSs.
    Kwok PY; Deng Q; Zakeri H; Taylor SL; Nickerson DA
    Genomics; 1996 Jan; 31(1):123-6. PubMed ID: 8808290
    [TBL] [Abstract][Full Text] [Related]  

  • 29. One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies.
    Yuan S; Johnston HR; Zhang G; Li Y; Hu YJ; Qin ZS
    PLoS Comput Biol; 2015 Aug; 11(8):e1004448. PubMed ID: 26267278
    [TBL] [Abstract][Full Text] [Related]  

  • 30. LEI: A Novel Allele Frequency-Based Feature Selection Method for Multi-ancestry Admixed Populations.
    Wathen MJ; Gautam Y; Ghandikota S; Rao MB; Mersha TB
    Sci Rep; 2019 Jul; 9(1):11103. PubMed ID: 31366927
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Deep sequencing to reveal new variants in pooled DNA samples.
    Out AA; van Minderhout IJ; Goeman JJ; Ariyurek Y; Ossowski S; Schneeberger K; Weigel D; van Galen M; Taschner PE; Tops CM; Breuning MH; van Ommen GJ; den Dunnen JT; Devilee P; Hes FJ
    Hum Mutat; 2009 Dec; 30(12):1703-12. PubMed ID: 19842214
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Maximum likelihood estimation of individual inbreeding coefficients and null allele frequencies.
    Hall N; Mercer L; Phillips D; Shaw J; Anderson AD
    Genet Res (Camb); 2012 Jun; 94(3):151-61. PubMed ID: 22805896
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A pipeline for local assembly of minisatellite alleles from single-molecule sequencing data.
    Ogeh D; Badge R
    Bioinformatics; 2017 Mar; 33(5):650-653. PubMed ID: 27998939
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Best linear unbiased allele-frequency estimation in complex pedigrees.
    McPeek MS; Wu X; Ober C
    Biometrics; 2004 Jun; 60(2):359-67. PubMed ID: 15180661
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterizing and interpreting genetic variation from personal genome sequencing.
    Johansson AC; Feuk L
    Methods Mol Biol; 2012; 838():343-67. PubMed ID: 22228021
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Quantification of rare allelic variants from pooled genomic DNA.
    Druley TE; Vallania FL; Wegner DJ; Varley KE; Knowles OL; Bonds JA; Robison SW; Doniger SW; Hamvas A; Cole FS; Fay JC; Mitra RD
    Nat Methods; 2009 Apr; 6(4):263-5. PubMed ID: 19252504
    [TBL] [Abstract][Full Text] [Related]  

  • 37. PoooL: an efficient method for estimating haplotype frequencies from large DNA pools.
    Zhang H; Yang HC; Yang Y
    Bioinformatics; 2008 Sep; 24(17):1942-8. PubMed ID: 18573795
    [TBL] [Abstract][Full Text] [Related]  

  • 38. KmerStream: streaming algorithms for k-mer abundance estimation.
    Melsted P; Halldórsson BV
    Bioinformatics; 2014 Dec; 30(24):3541-7. PubMed ID: 25355787
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Improvement in detection of minor alleles in next generation sequencing by base quality recalibration.
    Ni S; Stoneking M
    BMC Genomics; 2016 Feb; 17():139. PubMed ID: 26920804
    [TBL] [Abstract][Full Text] [Related]  

  • 40. SNP discovery in swine by reduced representation and high throughput pyrosequencing.
    Wiedmann RT; Smith TP; Nonneman DJ
    BMC Genet; 2008 Dec; 9():81. PubMed ID: 19055830
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.