Fang L - Search Results

1

Detection of DNA base modifications by deep recurrent neural network on Oxford Nanopore sequencing data.

Liu Q, Fang L, Yu G, Wang D, Xiao CL, Wang K. Liu Q, et al. Among authors: fang l. Nat Commun. 2019 Jun 4;10(1):2449. doi: 10.1038/s41467-019-10168-2. Nat Commun. 2019. PMID: 31164644 Free PMC article.

2

NextSV: a meta-caller for structural variants from low-coverage long-read sequencing data.

Fang L, Hu J, Wang D, Wang K. Fang L, et al. BMC Bioinformatics. 2018 May 23;19(1):180. doi: 10.1186/s12859-018-2207-1. BMC Bioinformatics. 2018. PMID: 29792160 Free PMC article.

3

Identification of Copy Number Variants from SNP Arrays Using PennCNV.

Fang L, Wang K. Fang L, et al. Methods Mol Biol. 2018;1833:1-28. doi: 10.1007/978-1-4939-8666-8_1. Methods Mol Biol. 2018. PMID: 30039360

4

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy.

Zeng S, Zhang MY, Wang XJ, Hu ZM, Li JC, Li N, Wang JL, Liang F, Yang Q, Liu Q, Fang L, Hao JW, Shi FD, Ding XB, Teng JF, Yin XM, Jiang H, Liao WP, Liu JY, Wang K, Xia K, Tang BS. Zeng S, et al. Among authors: fang l. J Med Genet. 2019 Apr;56(4):265-270. doi: 10.1136/jmedgenet-2018-105484. Epub 2018 Sep 7. J Med Genet. 2019. PMID: 30194086

5

Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD).

Dai Y, Li P, Wang Z, Liang F, Yang F, Fang L, Huang Y, Huang S, Zhou J, Wang D, Cui L, Wang K. Dai Y, et al. Among authors: fang l. J Med Genet. 2020 Feb;57(2):109-120. doi: 10.1136/jmedgenet-2019-106078. Epub 2019 Sep 10. J Med Genet. 2020. PMID: 31506324 Free PMC article.

6

Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophies.

Ling C, Dai Y, Fang L, Yao F, Liu Z, Qiu Z, Cui L, Xia F, Zhao C, Zhang S, Wang K, Zhang X. Ling C, et al. Among authors: fang l. Hum Mutat. 2020 Mar;41(3):668-677. doi: 10.1002/humu.23953. Epub 2019 Dec 3. Hum Mutat. 2020. PMID: 31705731 Free PMC article.

7

LinkedSV for detection of mosaic structural variants from linked-read exome and genome sequencing data.

Fang L, Kao C, Gonzalez MV, Mafra FA, Pellegrino da Silva R, Li M, Wenzel SS, Wimmer K, Hakonarson H, Wang K. Fang L, et al. Nat Commun. 2019 Dec 6;10(1):5585. doi: 10.1038/s41467-019-13397-7. Nat Commun. 2019. PMID: 31811119 Free PMC article.

8

Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases.

Zhao M, Havrilla JM, Fang L, Chen Y, Peng J, Liu C, Wu C, Sarmady M, Botas P, Isla J, Lyon GJ, Weng C, Wang K. Zhao M, et al. Among authors: fang l. NAR Genom Bioinform. 2020 Jun;2(2):lqaa032. doi: 10.1093/nargab/lqaa032. Epub 2020 May 25. NAR Genom Bioinform. 2020. PMID: 32500119 Free PMC article.

9

Implications of Error-Prone Long-Read Whole-Genome Shotgun Sequencing on Characterizing Reference Microbiomes.

Hu Y, Fang L, Nicholson C, Wang K. Hu Y, et al. Among authors: fang l. iScience. 2020 Jun 26;23(6):101223. doi: 10.1016/j.isci.2020.101223. Epub 2020 Jun 2. iScience. 2020. PMID: 32563152 Free PMC article.

10

A map of cis-regulatory elements and 3D genome structures in zebrafish.

Yang H, Luan Y, Liu T, Lee HJ, Fang L, Wang Y, Wang X, Zhang B, Jin Q, Ang KC, Xing X, Wang J, Xu J, Song F, Sriranga I, Khunsriraksakul C, Salameh T, Li D, Choudhary MNK, Topczewski J, Wang K, Gerhard GS, Hardison RC, Wang T, Cheng KC, Yue F. Yang H, et al. Among authors: fang l. Nature. 2020 Dec;588(7837):337-343. doi: 10.1038/s41586-020-2962-9. Epub 2020 Nov 25. Nature. 2020. PMID: 33239788 Free PMC article.

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