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 *

186 related articles for article (PubMed ID: 18562660)

  • 1. Testing for neutrality in samples with sequencing errors.
    Achaz G
    Genetics; 2008 Jul; 179(3):1409-24. PubMed ID: 18562660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Population genomics from pool sequencing.
    Ferretti L; Ramos-Onsins SE; Pérez-Enciso M
    Mol Ecol; 2013 Nov; 22(22):5561-76. PubMed ID: 24102736
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neutrality tests for sequences with missing data.
    Ferretti L; Raineri E; Ramos-Onsins S
    Genetics; 2012 Aug; 191(4):1397-401. PubMed ID: 22661328
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Fully Bayesian tests of neutrality using genealogical summary statistics.
    Drummond AJ; Suchard MA
    BMC Genet; 2008 Oct; 9():68. PubMed ID: 18976476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A General Framework for Neutrality Tests Based on the Site Frequency Spectrum.
    Ramos-Onsins SE; Marmorini G; Achaz G; Ferretti L
    Genes (Basel); 2023 Aug; 14(9):. PubMed ID: 37761854
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Frequency spectrum neutrality tests: one for all and all for one.
    Achaz G
    Genetics; 2009 Sep; 183(1):249-58. PubMed ID: 19546320
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Statistical power analysis of neutrality tests under demographic expansions, contractions and bottlenecks with recombination.
    Ramírez-Soriano A; Ramos-Onsins SE; Rozas J; Calafell F; Navarro A
    Genetics; 2008 May; 179(1):555-67. PubMed ID: 18493071
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Site Frequency/Dosage Spectrum of Autopolyploid Populations.
    Ferretti L; Ribeca P; Ramos-Onsins SE
    Front Genet; 2018; 9():480. PubMed ID: 30405691
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inferring population mutation rate and sequencing error rate using the SNP frequency spectrum in a sample of DNA sequences.
    Liu X; Maxwell TJ; Boerwinkle E; Fu YX
    Mol Biol Evol; 2009 Jul; 26(7):1479-90. PubMed ID: 19318520
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correcting for Sample Contamination in Genotype Calling of DNA Sequence Data.
    Flickinger M; Jun G; Abecasis GR; Boehnke M; Kang HM
    Am J Hum Genet; 2015 Aug; 97(2):284-90. PubMed ID: 26235984
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications.
    Arbeithuber B; Makova KD; Tiemann-Boege I
    DNA Res; 2016 Dec; 23(6):547-559. PubMed ID: 27477585
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Accounting for uncertainty in DNA sequencing data.
    O'Rawe JA; Ferson S; Lyon GJ
    Trends Genet; 2015 Feb; 31(2):61-6. PubMed ID: 25579994
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Statistical modeling for sensitive detection of low-frequency single nucleotide variants.
    Hao Y; Zhang P; Xuei X; Nakshatri H; Edenberg HJ; Li L; Liu Y
    BMC Genomics; 2016 Aug; 17 Suppl 7(Suppl 7):514. PubMed ID: 27556804
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of mixups among DNA sequencing plates.
    Stojanovic N; Chang JL; Lehoczky J; Zody MC; Dewar K
    Bioinformatics; 2002 Nov; 18(11):1418-26. PubMed ID: 12424111
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gap statistics for whole genome shotgun DNA sequencing projects.
    Wendl MC; Yang SP
    Bioinformatics; 2004 Jul; 20(10):1527-34. PubMed ID: 14962917
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Statistical modeling of sequencing errors in SAGE libraries.
    Beissbarth T; Hyde L; Smyth GK; Job C; Boon WM; Tan SS; Scott HS; Speed TP
    Bioinformatics; 2004 Aug; 20 Suppl 1():i31-9. PubMed ID: 15262778
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Modeling sequencing errors by combining Hidden Markov models.
    Lottaz C; Iseli C; Jongeneel CV; Bucher P
    Bioinformatics; 2003 Oct; 19 Suppl 2():ii103-12. PubMed ID: 14534179
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Correction of sequence-based artifacts in serial analysis of gene expression.
    Akmaev VR; Wang CJ
    Bioinformatics; 2004 May; 20(8):1254-63. PubMed ID: 14871862
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Multivariate QST-FST comparisons: a neutrality test for the evolution of the g matrix in structured populations.
    Martin G; Chapuis E; Goudet J
    Genetics; 2008 Dec; 180(4):2135-49. PubMed ID: 18245845
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An error correction strategy for image reconstruction by DNA sequencing microscopy.
    Kloosterman A; Baars I; Högberg B
    Nat Comput Sci; 2024 Feb; 4(2):119-127. PubMed ID: 38253805
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.