Liu X - Search Results

1

Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.

Dong C, Wei P, Jian X, Gibbs R, Boerwinkle E, Wang K, Liu X. Dong C, et al. Among authors: liu x. Hum Mol Genet. 2015 Apr 15;24(8):2125-37. doi: 10.1093/hmg/ddu733. Epub 2014 Dec 30. Hum Mol Genet. 2015. PMID: 25552646 Free PMC article.

2

dbNSFP: a lightweight database of human nonsynonymous SNPs and their functional predictions.

Liu X, Jian X, Boerwinkle E. Liu X, et al. Hum Mutat. 2011 Aug;32(8):894-9. doi: 10.1002/humu.21517. Hum Mutat. 2011. PMID: 21520341 Free PMC article.

3

dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.

Liu X, Jian X, Boerwinkle E. Liu X, et al. Hum Mutat. 2013 Sep;34(9):E2393-402. doi: 10.1002/humu.22376. Epub 2013 Jul 10. Hum Mutat. 2013. PMID: 23843252 Free PMC article.

4

In silico tools for splicing defect prediction: a survey from the viewpoint of end users.

Jian X, Boerwinkle E, Liu X. Jian X, et al. Among authors: liu x. Genet Med. 2014 Jul;16(7):497-503. doi: 10.1038/gim.2013.176. Epub 2013 Nov 21. Genet Med. 2014. PMID: 24263461 Free PMC article. Review.

5

WGSA: an annotation pipeline for human genome sequencing studies.

Liu X, White S, Peng B, Johnson AD, Brody JA, Li AH, Huang Z, Carroll A, Wei P, Gibbs R, Klein RJ, Boerwinkle E. Liu X, et al. J Med Genet. 2016 Feb;53(2):111-2. doi: 10.1136/jmedgenet-2015-103423. Epub 2015 Sep 22. J Med Genet. 2016. PMID: 26395054 Free PMC article. No abstract available.

6

dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs.

Liu X, Wu C, Li C, Boerwinkle E. Liu X, et al. Hum Mutat. 2016 Mar;37(3):235-41. doi: 10.1002/humu.22932. Epub 2016 Jan 5. Hum Mutat. 2016. PMID: 26555599 Free PMC article.

7

FLAGS: A Flexible and Adaptive Association Test for Gene Sets Using Summary Statistics.

Huang J, Wang K, Wei P, Liu X, Liu X, Tan K, Boerwinkle E, Potash JB, Han S. Huang J, et al. Among authors: liu x. Genetics. 2016 Mar;202(3):919-29. doi: 10.1534/genetics.115.185009. Epub 2016 Jan 15. Genetics. 2016. PMID: 26773050 Free PMC article.

8

In Silico Prediction of Deleteriousness for Nonsynonymous and Splice-Altering Single Nucleotide Variants in the Human Genome.

Jian X, Liu X. Jian X, et al. Among authors: liu x. Methods Mol Biol. 2017;1498:191-197. doi: 10.1007/978-1-4939-6472-7_13. Methods Mol Biol. 2017. PMID: 27709577

9

The performance of deleteriousness prediction scores for rare non-protein-changing single nucleotide variants in human genes.

Liu X, Li C, Boerwinkle E. Liu X, et al. J Med Genet. 2017 Feb;54(2):134-144. doi: 10.1136/jmedgenet-2016-104369. Epub 2016 Dec 20. J Med Genet. 2017. PMID: 27999115 Free PMC article. No abstract available.

10

Practical Approaches for Whole-Genome Sequence Analysis of Heart- and Blood-Related Traits.

Morrison AC, Huang Z, Yu B, Metcalf G, Liu X, Ballantyne C, Coresh J, Yu F, Muzny D, Feofanova E, Rustagi N, Gibbs R, Boerwinkle E. Morrison AC, et al. Among authors: liu x. Am J Hum Genet. 2017 Feb 2;100(2):205-215. doi: 10.1016/j.ajhg.2016.12.009. Epub 2017 Jan 12. Am J Hum Genet. 2017. PMID: 28089252 Free PMC article.

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