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.
83 related articles for article (PubMed ID: 20812911)
21. DoEstRare: A statistical test to identify local enrichments in rare genomic variants associated with disease. Persyn E; Karakachoff M; Le Scouarnec S; Le Clézio C; Campion D; Consortium FE; Schott JJ; Redon R; Bellanger L; Dina C PLoS One; 2017; 12(7):e0179364. PubMed ID: 28742119 [TBL] [Abstract][Full Text] [Related]
22. SNP frequency estimation using massively parallel sequencing of pooled DNA. Ingman M; Gyllensten U Eur J Hum Genet; 2009 Mar; 17(3):383-6. PubMed ID: 18854868 [TBL] [Abstract][Full Text] [Related]
23. The theory of discovering rare variants via DNA sequencing. Wendl MC; Wilson RK BMC Genomics; 2009 Oct; 10():485. PubMed ID: 19843339 [TBL] [Abstract][Full Text] [Related]
24. GenomeVIP: a cloud platform for genomic variant discovery and interpretation. Mashl RJ; Scott AD; Huang KL; Wyczalkowski MA; Yoon CJ; Niu B; DeNardo E; Yellapantula VD; Handsaker RE; Chen K; Koboldt DC; Ye K; Fenyö D; Raphael BJ; Wendl MC; Ding L Genome Res; 2017 Aug; 27(8):1450-1459. PubMed ID: 28522612 [TBL] [Abstract][Full Text] [Related]
25. 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]
26. India Allele Finder: a web-based annotation tool for identifying common alleles in next-generation sequencing data of Indian origin. Zhang JF; James F; Shukla A; Girisha KM; Paciorkowski AR BMC Res Notes; 2017 Jun; 10(1):233. PubMed ID: 28655339 [TBL] [Abstract][Full Text] [Related]
27. Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized Medicine. Bean LJ; Hegde MR Hum Mutat; 2016 Jun; 37(6):559-63. PubMed ID: 26931283 [TBL] [Abstract][Full Text] [Related]
28. Characterization and identification of hidden rare variants in the human genome. Magi A; D'Aurizio R; Palombo F; Cifola I; Tattini L; Semeraro R; Pippucci T; Giusti B; Romeo G; Abbate R; Gensini GF BMC Genomics; 2015 Apr; 16(1):340. PubMed ID: 25903059 [TBL] [Abstract][Full Text] [Related]
29. Impact of the 1000 genomes project on the next wave of pharmacogenomic discovery. Zhang W; Dolan ME Pharmacogenomics; 2010 Feb; 11(2):249-56. PubMed ID: 20136363 [TBL] [Abstract][Full Text] [Related]
30. Assessing the Power of Exome Chips. Page CM; Baranzini SE; Mevik BH; Bos SD; Harbo HF; Andreassen BK PLoS One; 2015; 10(10):e0139642. PubMed ID: 26437075 [TBL] [Abstract][Full Text] [Related]
31. Identifying rare variants with optimal depth of coverage and cost-effective overlapping pool sequencing. Cao CC; Li C; Huang Z; Ma X; Sun X Genet Epidemiol; 2013 Dec; 37(8):820-30. PubMed ID: 24166758 [TBL] [Abstract][Full Text] [Related]
32. A new testing strategy to identify rare variants with either risk or protective effect on disease. Ionita-Laza I; Buxbaum JD; Laird NM; Lange C PLoS Genet; 2011 Feb; 7(2):e1001289. PubMed ID: 21304886 [TBL] [Abstract][Full Text] [Related]
33. A Sparse Learning Framework for Joint Effect Analysis of Copy Number Variants. Wang Z; Hall B; Xu J; Shi X IEEE/ACM Trans Comput Biol Bioinform; 2017; 14(5):1013-1027. PubMed ID: 28991724 [TBL] [Abstract][Full Text] [Related]
34. [Detection and interpretation of somatic variants in molecular pathology]. Merkelbach-Bruse S; Rehker J; Siemanowski J; Klauschen F Pathologe; 2019 May; 40(3):243-249. PubMed ID: 31037375 [TBL] [Abstract][Full Text] [Related]
35. Confounded by sequencing depth in association studies of rare alleles. Garner C Genet Epidemiol; 2011 May; 35(4):261-8. PubMed ID: 21328616 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Integrating sequencing technologies in personal genomics: optimal low cost reconstruction of structural variants. Du J; Bjornson RD; Zhang ZD; Kong Y; Snyder M; Gerstein MB PLoS Comput Biol; 2009 Jul; 5(7):e1000432. PubMed ID: 19593373 [TBL] [Abstract][Full Text] [Related]
38. A variant by any name: quantifying annotation discordance across tools and clinical databases. Yen JL; Garcia S; Montana A; Harris J; Chervitz S; Morra M; West J; Chen R; Church DM Genome Med; 2017 Jan; 9(1):7. PubMed ID: 28122645 [TBL] [Abstract][Full Text] [Related]
39. An Incomplete Understanding of Human Genetic Variation. Huddleston J; Eichler EE Genetics; 2016 Apr; 202(4):1251-4. PubMed ID: 27053122 [TBL] [Abstract][Full Text] [Related]