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 *

122 related articles for article (PubMed ID: 35794006)

  • 1. Haplotype and population structure inference using neural networks in whole-genome sequencing data.
    Meisner J; Albrechtsen A
    Genome Res; 2022 Aug; 32(8):1542-1552. PubMed ID: 35794006
    [TBL] [Abstract][Full Text] [Related]  

  • 2. De novo inference of stratification and local admixture in sequencing studies.
    Zhang Y
    BMC Bioinformatics; 2013; 14 Suppl 5(Suppl 5):S17. PubMed ID: 23734678
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Improving population scale statistical phasing with whole-genome sequencing data.
    Wertenbroek R; Hofmeister RJ; Xenarios I; Thoma Y; Delaneau O
    PLoS Genet; 2024 Jul; 20(7):e1011092. PubMed ID: 38959269
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Modeling Human Population Separation History Using Physically Phased Genomes.
    Song S; Sliwerska E; Emery S; Kidd JM
    Genetics; 2017 Jan; 205(1):385-395. PubMed ID: 28049708
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hybrid autoencoder with orthogonal latent space for robust population structure inference.
    Yuan M; Hoskens H; Goovaerts S; Herrick N; Shriver MD; Walsh S; Claes P
    Sci Rep; 2023 Feb; 13(1):2612. PubMed ID: 36788253
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data.
    Yang WY; Hormozdiari F; Wang Z; He D; Pasaniuc B; Eskin E
    Bioinformatics; 2013 Sep; 29(18):2245-52. PubMed ID: 23825370
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ancestry inference using reference labeled clusters of haplotypes.
    Wang Y; Song S; Schraiber JG; Sedghifar A; Byrnes JK; Turissini DA; Hong EL; Ball CA; Noto K
    BMC Bioinformatics; 2021 Sep; 22(1):459. PubMed ID: 34563119
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inference of population structure using dense haplotype data.
    Lawson DJ; Hellenthal G; Myers S; Falush D
    PLoS Genet; 2012 Jan; 8(1):e1002453. PubMed ID: 22291602
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inferring Population Structure and Admixture Proportions in Low-Depth NGS Data.
    Meisner J; Albrechtsen A
    Genetics; 2018 Oct; 210(2):719-731. PubMed ID: 30131346
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A deep learning framework for characterization of genotype data.
    Ausmees K; Nettelblad C
    G3 (Bethesda); 2022 Mar; 12(3):. PubMed ID: 35078229
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Haplotype inference and block partitioning in mixed population samples.
    Sazonova N; Harner EJ
    J Bioinform Comput Biol; 2008 Dec; 6(6):1177-92. PubMed ID: 19090023
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hap-seq: an optimal algorithm for haplotype phasing with imputation using sequencing data.
    He D; Han B; Eskin E
    J Comput Biol; 2013 Feb; 20(2):80-92. PubMed ID: 23383995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ancestry inference using principal component analysis and spatial analysis: a distance-based analysis to account for population substructure.
    Byun J; Han Y; Gorlov IP; Busam JA; Seldin MF; Amos CI
    BMC Genomics; 2017 Oct; 18(1):789. PubMed ID: 29037167
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haplotype inference from unphased SNP data in heterozygous polyploids based on SAT.
    Neigenfind J; Gyetvai G; Basekow R; Diehl S; Achenbach U; Gebhardt C; Selbig J; Kersten B
    BMC Genomics; 2008 Jul; 9():356. PubMed ID: 18667059
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Integrating read-based and population-based phasing for dense and accurate haplotyping of individual genomes.
    Bansal V
    Bioinformatics; 2019 Jul; 35(14):i242-i248. PubMed ID: 31510646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations.
    Bansal V; Libiger O
    BMC Bioinformatics; 2015 Jan; 16():4. PubMed ID: 25592880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Joint haplotype assembly and genotype calling via sequential Monte Carlo algorithm.
    Ahn S; Vikalo H
    BMC Bioinformatics; 2015 Jul; 16():223. PubMed ID: 26178880
    [TBL] [Abstract][Full Text] [Related]  

  • 18. fastNGSadmix: admixture proportions and principal component analysis of a single NGS sample.
    Jørsboe E; Hanghøj K; Albrechtsen A
    Bioinformatics; 2017 Oct; 33(19):3148-3150. PubMed ID: 28957500
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparison of haplotype inference methods using genotypic data from unrelated individuals.
    Xu H; Wu X; Spitz MR; Shete S
    Hum Hered; 2004; 58(2):63-8. PubMed ID: 15711085
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Colloquium paper: genome-wide patterns of population structure and admixture among Hispanic/Latino populations.
    Bryc K; Velez C; Karafet T; Moreno-Estrada A; Reynolds A; Auton A; Hammer M; Bustamante CD; Ostrer H
    Proc Natl Acad Sci U S A; 2010 May; 107 Suppl 2(Suppl 2):8954-61. PubMed ID: 20445096
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.