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.
441 related articles for article (PubMed ID: 20552648)
1. Design of association studies with pooled or un-pooled next-generation sequencing data. Kim SY; Li Y; Guo Y; Li R; Holmkvist J; Hansen T; Pedersen O; Wang J; Nielsen R Genet Epidemiol; 2010 Jul; 34(5):479-91. PubMed ID: 20552648 [TBL] [Abstract][Full Text] [Related]
2. Analysis and optimal design for association studies using next-generation sequencing with case-control pools. Liang WE; Thomas DC; Conti DV Genet Epidemiol; 2012 Dec; 36(8):870-81. PubMed ID: 22972696 [TBL] [Abstract][Full Text] [Related]
3. Resequencing of pooled DNA for detecting disease associations with rare variants. Wang T; Lin CY; Rohan TE; Ye K Genet Epidemiol; 2010 Jul; 34(5):492-501. PubMed ID: 20578089 [TBL] [Abstract][Full Text] [Related]
4. A unified approach for allele frequency estimation, SNP detection and association studies based on pooled sequencing data using EM algorithms. Chen Q; Sun F BMC Genomics; 2013; 14 Suppl 1(Suppl 1):S1. PubMed ID: 23369070 [TBL] [Abstract][Full Text] [Related]
5. The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA. Chiang CW; Gajdos ZK; Korn JM; Butler JL; Hackett R; Guiducci C; Nguyen TT; Wilks R; Forrester T; Henderson KD; Le Marchand L; Henderson BE; Haiman CA; Cooper RS; Lyon HN; Zhu X; McKenzie CA; Palmert MR; Hirschhorn JN Hum Genet; 2011 Nov; 130(5):607-21. PubMed ID: 21424828 [TBL] [Abstract][Full Text] [Related]
6. Large-scale detection of rare variants via pooled multiplexed next-generation sequencing: towards next-generation Ecotilling. Marroni F; Pinosio S; Di Centa E; Jurman I; Boerjan W; Felice N; Cattonaro F; Morgante M Plant J; 2011 Aug; 67(4):736-45. PubMed ID: 21554453 [TBL] [Abstract][Full Text] [Related]
7. On optimal pooling designs to identify rare variants through massive resequencing. Lee JS; Choi M; Yan X; Lifton RP; Zhao H Genet Epidemiol; 2011 Apr; 35(3):139-47. PubMed ID: 21254222 [TBL] [Abstract][Full Text] [Related]
8. Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling. Ji F; Finch SJ; Haynes C; Mendell NR; Gordon D BMC Genomics; 2007 Jul; 8():238. PubMed ID: 17634103 [TBL] [Abstract][Full Text] [Related]
9. On the use of DNA pooling to estimate haplotype frequencies. Wang S; Kidd KK; Zhao H Genet Epidemiol; 2003 Jan; 24(1):74-82. PubMed ID: 12508258 [TBL] [Abstract][Full Text] [Related]
10. Biases and errors on allele frequency estimation and disease association tests of next-generation sequencing of pooled samples. Chen X; Listman JB; Slack FJ; Gelernter J; Zhao H Genet Epidemiol; 2012 Sep; 36(6):549-60. PubMed ID: 22674656 [TBL] [Abstract][Full Text] [Related]
11. Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer's Disease. Jin SC; Benitez BA; Deming Y; Cruchaga C Methods Mol Biol; 2016; 1303():299-314. PubMed ID: 26235075 [TBL] [Abstract][Full Text] [Related]
12. A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data. Luo L; Zhu Y; Xiong M J Comput Biol; 2012 Jun; 19(6):731-44. PubMed ID: 22651812 [TBL] [Abstract][Full Text] [Related]
13. Estimation of population allele frequencies from next-generation sequencing data: pool-versus individual-based genotyping. Gautier M; Foucaud J; Gharbi K; Cézard T; Galan M; Loiseau A; Thomson M; Pudlo P; Kerdelhué C; Estoup A Mol Ecol; 2013 Jul; 22(14):3766-79. PubMed ID: 23730833 [TBL] [Abstract][Full Text] [Related]
14. Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. Kim W; Londono D; Zhou L; Xing J; Nato AQ; Musolf A; Matise TC; Finch SJ; Gordon D Hum Hered; 2012; 74(3-4):172-83. PubMed ID: 23594495 [TBL] [Abstract][Full Text] [Related]
15. Efficient study design for next generation sequencing. Sampson J; Jacobs K; Yeager M; Chanock S; Chatterjee N Genet Epidemiol; 2011 May; 35(4):269-77. PubMed ID: 21370254 [TBL] [Abstract][Full Text] [Related]
16. An efficient study design to test parent-of-origin effects in family trios. Yu X; Chen G; Feng R Genet Epidemiol; 2017 Nov; 41(7):587-598. PubMed ID: 28726280 [TBL] [Abstract][Full Text] [Related]
17. An evaluation of statistical approaches to rare variant analysis in genetic association studies. Morris AP; Zeggini E Genet Epidemiol; 2010 Feb; 34(2):188-93. PubMed ID: 19810025 [TBL] [Abstract][Full Text] [Related]
18. SNP calling by sequencing pooled samples. Raineri E; Ferretti L; Esteve-Codina A; Nevado B; Heath S; Pérez-Enciso M BMC Bioinformatics; 2012 Sep; 13():239. PubMed ID: 22992255 [TBL] [Abstract][Full Text] [Related]
19. Evaluation of allele frequency estimation using pooled sequencing data simulation. Guo Y; Samuels DC; Li J; Clark T; Li CI; Shyr Y ScientificWorldJournal; 2013; 2013():895496. PubMed ID: 23476151 [TBL] [Abstract][Full Text] [Related]
20. Estimating allele frequency from next-generation sequencing of pooled mitochondrial DNA samples. Wang T; Pradhan K; Ye K; Wong LJ; Rohan TE Front Genet; 2011; 2():51. PubMed ID: 22303347 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]