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 *

266 related articles for article (PubMed ID: 16287933)

  • 1. 2SNP: scalable phasing based on 2-SNP haplotypes.
    Brinza D; Zelikovsky A
    Bioinformatics; 2006 Feb; 22(3):371-3. PubMed ID: 16287933
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 2SNP: scalable phasing method for trios and unrelated individuals.
    Brinza D; Zelikovsky A
    IEEE/ACM Trans Comput Biol Bioinform; 2008; 5(2):313-8. PubMed ID: 18451440
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.
    Di X; Matsuzaki H; Webster TA; Hubbell E; Liu G; Dong S; Bartell D; Huang J; Chiles R; Yang G; Shen MM; Kulp D; Kennedy GC; Mei R; Jones KW; Cawley S
    Bioinformatics; 2005 May; 21(9):1958-63. PubMed ID: 15657097
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.
    Matsuzaki H; Dong S; Loi H; Di X; Liu G; Hubbell E; Law J; Berntsen T; Chadha M; Hui H; Yang G; Kennedy GC; Webster TA; Cawley S; Walsh PS; Jones KW; Fodor SP; Mei R
    Nat Methods; 2004 Nov; 1(2):109-11. PubMed ID: 15782172
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inference of missing SNPs and information quantity measurements for haplotype blocks.
    Su SC; Kuo CC; Chen T
    Bioinformatics; 2005 May; 21(9):2001-7. PubMed ID: 15699029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SNP-PHAGE--High throughput SNP discovery pipeline.
    Matukumalli LK; Grefenstette JJ; Hyten DL; Choi IY; Cregan PB; Van Tassell CP
    BMC Bioinformatics; 2006 Oct; 7():468. PubMed ID: 17059604
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SEAN: SNP prediction and display program utilizing EST sequence clusters.
    Huntley D; Baldo A; Johri S; Sergot M
    Bioinformatics; 2006 Feb; 22(4):495-6. PubMed ID: 16357032
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inferring missing genotypes in large SNP panels using fast nearest-neighbor searches over sliding windows.
    Roberts A; McMillan L; Wang W; Parker J; Rusyn I; Threadgill D
    Bioinformatics; 2007 Jul; 23(13):i401-7. PubMed ID: 17646323
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Constructing near-perfect phylogenies with multiple homoplasy events.
    Satya RV; Mukherjee A; Alexe G; Parida L; Bhanot G
    Bioinformatics; 2006 Jul; 22(14):e514-22. PubMed ID: 16873515
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A parsimonious tree-grow method for haplotype inference.
    Li Z; Zhou W; Zhang XS; Chen L
    Bioinformatics; 2005 Sep; 21(17):3475-81. PubMed ID: 16002432
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GEVALT: an integrated software tool for genotype analysis.
    Davidovich O; Kimmel G; Shamir R
    BMC Bioinformatics; 2007 Feb; 8():36. PubMed ID: 17270038
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SNPs made routine.
    Broman KW; Feingold E
    Nat Methods; 2004 Nov; 1(2):104-5. PubMed ID: 15782170
    [No Abstract]   [Full Text] [Related]  

  • 13. Simulating association studies: a data-based resampling method for candidate regions or whole genome scans.
    Wright FA; Huang H; Guan X; Gamiel K; Jeffries C; Barry WT; de Villena FP; Sullivan PF; Wilhelmsen KC; Zou F
    Bioinformatics; 2007 Oct; 23(19):2581-8. PubMed ID: 17785348
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotype reconstruction from SNP fragments by minimum error correction.
    Wang RS; Wu LY; Li ZP; Zhang XS
    Bioinformatics; 2005 May; 21(10):2456-62. PubMed ID: 15731204
    [TBL] [Abstract][Full Text] [Related]  

  • 15. BNTagger: improved tagging SNP selection using Bayesian networks.
    Lee PH; Shatkay H
    Bioinformatics; 2006 Jul; 22(14):e211-9. PubMed ID: 16873474
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MLR-tagging: informative SNP selection for unphased genotypes based on multiple linear regression.
    He J; Zelikovsky A
    Bioinformatics; 2006 Oct; 22(20):2558-61. PubMed ID: 16895924
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome resequencing and genetic variation.
    Stratton M
    Nat Biotechnol; 2008 Jan; 26(1):65-6. PubMed ID: 18183021
    [No Abstract]   [Full Text] [Related]  

  • 18. A highly informative SNP linkage panel for human genetic studies.
    Murray SS; Oliphant A; Shen R; McBride C; Steeke RJ; Shannon SG; Rubano T; Kermani BG; Fan JB; Chee MS; Hansen MS
    Nat Methods; 2004 Nov; 1(2):113-7. PubMed ID: 15782173
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype reconstruction from genotype data using Imperfect Phylogeny.
    Halperin E; Eskin E
    Bioinformatics; 2004 Aug; 20(12):1842-9. PubMed ID: 14988101
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A greedier approach for finding tag SNPs.
    Chang CJ; Huang YT; Chao KM
    Bioinformatics; 2006 Mar; 22(6):685-91. PubMed ID: 16403792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.