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 *

183 related articles for article (PubMed ID: 35641757)

  • 21. Low-depth genotyping-by-sequencing (GBS) in a bovine population: strategies to maximize the selection of high quality genotypes and the accuracy of imputation.
    Brouard JS; Boyle B; Ibeagha-Awemu EM; Bissonnette N
    BMC Genet; 2017 Apr; 18(1):32. PubMed ID: 28381212
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets.
    Li MX; Yeung JM; Cherny SS; Sham PC
    Hum Genet; 2012 May; 131(5):747-56. PubMed ID: 22143225
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Simple SNP-based minimal marker genotyping for Humulus lupulus L. identification and variety validation.
    Henning JA; Coggins J; Peterson M
    BMC Res Notes; 2015 Oct; 8():542. PubMed ID: 26438052
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays.
    Li JH; Mazur CA; Berisa T; Pickrell JK
    Genome Res; 2021 Apr; 31(4):529-537. PubMed ID: 33536225
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Recommendations for Choosing the Genotyping Method and Best Practices for Quality Control in Crop Genome-Wide Association Studies.
    Pavan S; Delvento C; Ricciardi L; Lotti C; Ciani E; D'Agostino N
    Front Genet; 2020; 11():447. PubMed ID: 32587600
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High-throughput phenotyping for crop improvement in the genomics era.
    Mir RR; Reynolds M; Pinto F; Khan MA; Bhat MA
    Plant Sci; 2019 May; 282():60-72. PubMed ID: 31003612
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Accurate Imputation of Untyped Variants from Deep Sequencing Data.
    Torkamaneh D; Belzile F
    Methods Mol Biol; 2021; 2243():271-281. PubMed ID: 33606262
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Integration of Infinium and Axiom SNP array data in the outcrossing species Malus × domestica and causes for seemingly incompatible calls.
    Howard NP; Troggio M; Durel CE; Muranty H; Denancé C; Bianco L; Tillman J; van de Weg E
    BMC Genomics; 2021 Apr; 22(1):246. PubMed ID: 33827434
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotyping-by-sequencing and SNP-arrays are complementary for detecting quantitative trait loci by tagging different haplotypes in association studies.
    Negro SS; Millet EJ; Madur D; Bauland C; Combes V; Welcker C; Tardieu F; Charcosset A; Nicolas SD
    BMC Plant Biol; 2019 Jul; 19(1):318. PubMed ID: 31311506
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Role of NGS and SNP genotyping methods in sugarcane improvement programs.
    Manimekalai R; Suresh G; Govinda Kurup H; Athiappan S; Kandalam M
    Crit Rev Biotechnol; 2020 Sep; 40(6):865-880. PubMed ID: 32508157
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics.
    Wasik K; Berisa T; Pickrell JK; Li JH; Fraser DJ; King K; Cox C
    BMC Genomics; 2021 Mar; 22(1):197. PubMed ID: 33743587
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Strategies for processing and quality control of Illumina genotyping arrays.
    Zhao S; Jing W; Samuels DC; Sheng Q; Shyr Y; Guo Y
    Brief Bioinform; 2018 Sep; 19(5):765-775. PubMed ID: 28334151
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole-Genome Genotyping Using DNA Microarrays for Population Genetics.
    Van Asselt AJ; Ehli EA
    Methods Mol Biol; 2022; 2418():269-287. PubMed ID: 35119671
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Development and Applications of a High Throughput Genotyping Tool for Polyploid Crops: Single Nucleotide Polymorphism (SNP) Array.
    You Q; Yang X; Peng Z; Xu L; Wang J
    Front Plant Sci; 2018; 9():104. PubMed ID: 29467780
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genotyping-by-Sequencing and Its Application to Oat Genomic Research.
    Fu YB; Yang MH
    Methods Mol Biol; 2017; 1536():169-187. PubMed ID: 28132151
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies.
    Chat V; Ferguson R; Morales L; Kirchhoff T
    Front Genet; 2021; 12():790445. PubMed ID: 35251117
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Re-ranking sequencing variants in the post-GWAS era for accurate causal variant identification.
    Faye LL; Machiela MJ; Kraft P; Bull SB; Sun L
    PLoS Genet; 2013; 9(8):e1003609. PubMed ID: 23950724
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Saliva samples are a viable alternative to blood samples as a source of DNA for high throughput genotyping.
    Abraham JE; Maranian MJ; Spiteri I; Russell R; Ingle S; Luccarini C; Earl HM; Pharoah PP; Dunning AM; Caldas C
    BMC Med Genomics; 2012 May; 5():19. PubMed ID: 22647440
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-Wide SNP Calling from Genotyping by Sequencing (GBS) Data: A Comparison of Seven Pipelines and Two Sequencing Technologies.
    Torkamaneh D; Laroche J; Belzile F
    PLoS One; 2016; 11(8):e0161333. PubMed ID: 27547936
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Specific-Locus Amplified Fragment Sequencing (SLAF-Seq) as High-Throughput SNP Genotyping Methods.
    Zhu Z; Sun B; Lei J
    Methods Mol Biol; 2021; 2264():75-87. PubMed ID: 33263904
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.