Li X - Search Results

1

A single cell level based method for copy number variation analysis by low coverage massively parallel sequencing.

Zhang C, Zhang C, Chen S, Yin X, Pan X, Lin G, Tan Y, Tan K, Xu Z, Hu P, Li X, Chen F, Xu X, Li Y, Zhang X, Jiang H, Wang W. Zhang C, et al. Among authors: li y, li x. PLoS One. 2013;8(1):e54236. doi: 10.1371/journal.pone.0054236. Epub 2013 Jan 23. PLoS One. 2013. PMID: 23372689 Free PMC article.

2

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.

Yin X, Tan K, Vajta G, Jiang H, Tan Y, Zhang C, Chen F, Chen S, Zhang C, Pan X, Gong C, Li X, Lin C, Gao Y, Liang Y, Yi X, Mu F, Zhao L, Peng H, Xiong B, Zhang S, Cheng D, Lu G, Zhang X, Lin G, Wang W. Yin X, et al. Among authors: li x. Biol Reprod. 2013 Mar 21;88(3):69. doi: 10.1095/biolreprod.112.106211. Print 2013 Mar. Biol Reprod. 2013. PMID: 23349234

3

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing.

Chen S, Lau TK, Zhang C, Xu C, Xu Z, Hu P, Xu J, Huang H, Pan L, Jiang F, Chen F, Pan X, Xie W, Liu P, Li X, Zhang L, Li S, Li Y, Xu X, Wang W, Wang J, Jiang H, Zhang X. Chen S, et al. Among authors: li s, li y, li x. Prenat Diagn. 2013 Jun;33(6):584-90. doi: 10.1002/pd.4110. Prenat Diagn. 2013. PMID: 23592436

4

Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia.

Ge H, Huang X, Li X, Chen S, Zheng J, Jiang H, Zhang C, Pan X, Guo J, Chen F, Chen N, Fang Q, Jiang H, Wang W. Ge H, et al. Among authors: li x. PLoS One. 2013 Jun 28;8(6):e67464. doi: 10.1371/journal.pone.0067464. Print 2013. PLoS One. 2013. PMID: 23840709 Free PMC article.

5

PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.

Li X, Chen S, Xie W, Vogel I, Choy KW, Chen F, Christensen R, Zhang C, Ge H, Jiang H, Yu C, Huang F, Wang W, Jiang H, Zhang X. Li X, et al. PLoS One. 2014 Jan 21;9(1):e85096. doi: 10.1371/journal.pone.0085096. eCollection 2014. PLoS One. 2014. PMID: 24465483 Free PMC article.

6

Performance comparison between rapid sequencing platforms for ultra-low coverage sequencing strategy.

Chen S, Li S, Xie W, Li X, Zhang C, Jiang H, Zheng J, Pan X, Zheng H, Liu JS, Deng Y, Chen F, Jiang H. Chen S, et al. Among authors: li s, li x. PLoS One. 2014 Mar 20;9(3):e92192. doi: 10.1371/journal.pone.0092192. eCollection 2014. PLoS One. 2014. PMID: 24651575 Free PMC article.

7

Prenatal detection of aneuploidy and imbalanced chromosomal arrangements by massively parallel sequencing.

Dan S, Chen F, Choy KW, Jiang F, Lin J, Xuan Z, Wang W, Chen S, Li X, Jiang H, Leung TY, Lau TK, Su Y, Zhang W, Zhang X. Dan S, et al. Among authors: li x. PLoS One. 2012;7(2):e27835. doi: 10.1371/journal.pone.0027835. Epub 2012 Feb 28. PLoS One. 2012. PMID: 22389664 Free PMC article.

8

Rapid detection of aneuploidies on a benchtop sequencing platform.

Xie W, Tan Y, Li X, Lin G, Jiang H, Chen F, Zhang C, Gong F, Pan X, Chen S, Lu G, Wang W, Zhang X. Xie W, et al. Among authors: li x. Prenat Diagn. 2013 Mar;33(3):232-7. doi: 10.1002/pd.4049. Epub 2013 Jan 28. Prenat Diagn. 2013. PMID: 23359364

9

Haplotype-assisted accurate non-invasive fetal whole genome recovery through maternal plasma sequencing.

Chen S, Ge H, Wang X, Pan X, Yao X, Li X, Zhang C, Chen F, Jiang F, Li P, Jiang H, Zheng H, Zhang L, Zhao L, Wang W, Li S, Wang J, Wang J, Yang H, Li Y, Zhang X. Chen S, et al. Among authors: li s, li y, li x, li p. Genome Med. 2013 Feb 27;5(2):18. doi: 10.1186/gm422. eCollection 2013. Genome Med. 2013. PMID: 23445748 Free PMC article.

10

Effective noninvasive zygosity determination by maternal plasma target region sequencing.

Zheng J, Xu C, Guo J, Wei Y, Ge H, Li X, Zhang C, Jiang H, Pan L, Tang W, Xie W, Zhang H, Zhao Y, Jiang F, Chen S, Wang W, Xu X, Chen F, Huang H, Jiang H. Zheng J, et al. Among authors: li x. PLoS One. 2013 Jun 10;8(6):e65050. doi: 10.1371/journal.pone.0065050. Print 2013. PLoS One. 2013. PMID: 23762285 Free PMC article.

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