518 related articles for article (PubMed ID: 25568282)
1. A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysis.
Chen R; Wei Q; Zhan X; Zhong X; Sutcliffe JS; Cox NJ; Cook EH; Li C; Chen W; Li B
Bioinformatics; 2015 May; 31(9):1452-9. PubMed ID: 25568282
[TBL] [Abstract][Full Text] [Related]
2. Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.
He Z; O'Roak BJ; Smith JD; Wang G; Hooker S; Santos-Cortez RL; Li B; Kan M; Krumm N; Nickerson DA; Shendure J; Eichler EE; Leal SM
Am J Hum Genet; 2014 Jan; 94(1):33-46. PubMed ID: 24360806
[TBL] [Abstract][Full Text] [Related]
3. The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.
Guo W; Shugart YY
BMC Genomics; 2014 Jul; 15(1):632. PubMed ID: 25070353
[TBL] [Abstract][Full Text] [Related]
4. Gene Mapping in Admixed Families: A Cautionary Note on the Interpretation of the Transmission Disequilibrium Test and a Possible Solution.
Wang X; Xiao R; Zhu X; Li M
Hum Hered; 2016; 81(2):106-116. PubMed ID: 28076865
[TBL] [Abstract][Full Text] [Related]
5. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
DE LA Vega FM; Bustamante CD; Leal SM
Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
[TBL] [Abstract][Full Text] [Related]
6. The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.
He Z; Zhang D; Renton AE; Li B; Zhao L; Wang GT; Goate AM; Mayeux R; Leal SM
Am J Hum Genet; 2017 Feb; 100(2):193-204. PubMed ID: 28065470
[TBL] [Abstract][Full Text] [Related]
7. Haplotype sharing transmission/disequilibrium tests that allow for genotyping errors.
Sha Q; Dong J; Jiang R; Chen HS; Zhang S
Genet Epidemiol; 2005 May; 28(4):341-51. PubMed ID: 15662724
[TBL] [Abstract][Full Text] [Related]
8. Methods for association analysis and meta-analysis of rare variants in families.
Feng S; Pistis G; Zhang H; Zawistowski M; Mulas A; Zoledziewska M; Holmen OL; Busonero F; Sanna S; Hveem K; Willer C; Cucca F; Liu DJ; Abecasis GR
Genet Epidemiol; 2015 May; 39(4):227-38. PubMed ID: 25740221
[TBL] [Abstract][Full Text] [Related]
9. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
10. Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants.
Kinnamon DD; Hershberger RE; Martin ER
PLoS One; 2012; 7(2):e30238. PubMed ID: 22363423
[TBL] [Abstract][Full Text] [Related]
11. A Zoom-Focus algorithm (ZFA) to locate the optimal testing region for rare variant association tests.
Wang MH; Weng H; Sun R; Lee J; Wu WKK; Chong KC; Zee BC
Bioinformatics; 2017 Aug; 33(15):2330-2336. PubMed ID: 28334355
[TBL] [Abstract][Full Text] [Related]
12. Rare variant association test in family-based sequencing studies.
Wang X; Zhang Z; Morris N; Cai T; Lee S; Wang C; Yu TW; Walsh CA; Lin X
Brief Bioinform; 2017 Nov; 18(6):954-961. PubMed ID: 27677958
[TBL] [Abstract][Full Text] [Related]
13. A Bayesian framework for de novo mutation calling in parents-offspring trios.
Wei Q; Zhan X; Zhong X; Liu Y; Han Y; Chen W; Li B
Bioinformatics; 2015 May; 31(9):1375-81. PubMed ID: 25535243
[TBL] [Abstract][Full Text] [Related]
14. Testing the effect of rare compound-heterozygous and recessive mutations in case--parent sequencing studies.
Jiang Y; McCarthy JM; Allen AS
Genet Epidemiol; 2015 Mar; 39(3):166-72. PubMed ID: 25631493
[TBL] [Abstract][Full Text] [Related]
15. Region-based association tests for sequencing data on survival traits.
Chien LC; Bowden DW; Chiu YF
Genet Epidemiol; 2017 Sep; 41(6):511-522. PubMed ID: 28580640
[TBL] [Abstract][Full Text] [Related]
16. RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method.
Hamazaki K; Iwata H
PLoS Comput Biol; 2020 Feb; 16(2):e1007663. PubMed ID: 32059004
[TBL] [Abstract][Full Text] [Related]
17. A comparison of popular TDT-generalizations for family-based association analysis.
Hecker J; Laird N; Lange C
Genet Epidemiol; 2019 Apr; 43(3):300-317. PubMed ID: 30609057
[TBL] [Abstract][Full Text] [Related]
18. A power set-based statistical selection procedure to locate susceptible rare variants associated with complex traits with sequencing data.
Sun H; Wang S
Bioinformatics; 2014 Aug; 30(16):2317-23. PubMed ID: 24755303
[TBL] [Abstract][Full Text] [Related]
19. Weighted Transmission Disequilibrium Test for Family Trio Association Design.
Fang H; Yang Y; Chen L
Hum Hered; 2018; 83(4):196-209. PubMed ID: 30865952
[TBL] [Abstract][Full Text] [Related]
20. TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data.
Londono D; Buyske S; Finch SJ; Sharma S; Wise CA; Gordon D
BMC Bioinformatics; 2012 Jan; 13():13. PubMed ID: 22264315
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]