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 *

69 related articles for article (PubMed ID: 9520506)

  • 41. Next generation sequencing reads comparison with an alignment-free distance.
    Weitschek E; Santoni D; Fiscon G; De Cola MC; Bertolazzi P; Felici G
    BMC Res Notes; 2014 Dec; 7():869. PubMed ID: 25465386
    [TBL] [Abstract][Full Text] [Related]  

  • 42. An accurate algorithm for the detection of DNA fragments from dilution pool sequencing experiments.
    Bansal V
    Bioinformatics; 2018 Jan; 34(1):155-162. PubMed ID: 29036419
    [TBL] [Abstract][Full Text] [Related]  

  • 43. GMAP and GSNAP for Genomic Sequence Alignment: Enhancements to Speed, Accuracy, and Functionality.
    Wu TD; Reeder J; Lawrence M; Becker G; Brauer MJ
    Methods Mol Biol; 2016; 1418():283-334. PubMed ID: 27008021
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Rapid identification of single nucleotide substitutions using SeqDoC.
    Crowe ML
    Methods Mol Biol; 2007; 396():345-57. PubMed ID: 18025703
    [TBL] [Abstract][Full Text] [Related]  

  • 45. rHAT: fast alignment of noisy long reads with regional hashing.
    Liu B; Guan D; Teng M; Wang Y
    Bioinformatics; 2016 Jun; 32(11):1625-31. PubMed ID: 26568628
    [TBL] [Abstract][Full Text] [Related]  

  • 46. TargetIdentifier: a webserver for identifying full-length cDNAs from EST sequences.
    Min XJ; Butler G; Storms R; Tsang A
    Nucleic Acids Res; 2005 Jul; 33(Web Server issue):W669-72. PubMed ID: 15980559
    [TBL] [Abstract][Full Text] [Related]  

  • 47. A space-efficient algorithm for the constrained pairwise sequence alignment problem.
    He D; Arslan AN
    Genome Inform; 2005; 16(2):237-46. PubMed ID: 16901106
    [TBL] [Abstract][Full Text] [Related]  

  • 48. CUDA ClustalW: An efficient parallel algorithm for progressive multiple sequence alignment on Multi-GPUs.
    Hung CL; Lin YS; Lin CY; Chung YC; Chung YF
    Comput Biol Chem; 2015 Oct; 58():62-8. PubMed ID: 26052076
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Accurate anchoring alignment of divergent sequences.
    Huang W; Umbach DM; Li L
    Bioinformatics; 2006 Jan; 22(1):29-34. PubMed ID: 16301203
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Multiple sequence alignment based on profile alignment of intermediate sequences.
    Lu Y; Sze SH
    J Comput Biol; 2008 Sep; 15(7):767-77. PubMed ID: 18662101
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Making DNA add.
    Guarnieri F; Fliss M; Bancroft C
    Science; 1996 Jul; 273(5272):220-3. PubMed ID: 8662501
    [TBL] [Abstract][Full Text] [Related]  

  • 52. The evolution of molecular computation.
    Stemmer WP
    Science; 1995 Dec; 270(5241):1510. PubMed ID: 7491501
    [No Abstract]   [Full Text] [Related]  

  • 53. DNA sequencing.
    Rees WD
    Proc Nutr Soc; 1996 Mar; 55(1B):605-12. PubMed ID: 8832824
    [No Abstract]   [Full Text] [Related]  

  • 54. On the potential of molecular computing.
    Linial M; Linial N
    Science; 1995 Apr; 268(5210):481; author reply 483-4. PubMed ID: 7725085
    [No Abstract]   [Full Text] [Related]  

  • 55. Single nucleotide polymorphism mapping using genome-wide unique sequences.
    Chen LY; Lu SH; Shih ES; Hwang MJ
    Genome Res; 2002 Jul; 12(7):1106-11. PubMed ID: 12097348
    [TBL] [Abstract][Full Text] [Related]  

  • 56. DNA sequence chromatogram browsing using JAVA and CORBA.
    Parsons JD; Buehler E; Hillier L
    Genome Res; 1999 Mar; 9(3):277-81. PubMed ID: 10077534
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Sequence assembly with CAFTOOLS.
    Dear S; Durbin R; Hillier L; Marth G; Thierry-Mieg J; Mott R
    Genome Res; 1998 Mar; 8(3):260-7. PubMed ID: 9521929
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Trace alignment and some of its applications.
    Mott R
    Bioinformatics; 1998; 14(1):92-7. PubMed ID: 9520506
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Automated generation of heuristics for biological sequence comparison.
    Slater GS; Birney E
    BMC Bioinformatics; 2005 Feb; 6():31. PubMed ID: 15713233
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Automated detection of point mutations using fluorescent sequence trace subtraction.
    Bonfield JK; Rada C; Staden R
    Nucleic Acids Res; 1998 Jul; 26(14):3404-9. PubMed ID: 9649626
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.