Wang D - Search Results

1

Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform.

Hu L, Liang F, Cheng D, Zhang Z, Yu G, Zha J, Wang Y, Xia Q, Yuan D, Tan Y, Wang D, Liang Y, Lin G. Hu L, et al. Among authors: wang y, wang d. Front Genet. 2020 Jan 14;10:1313. doi: 10.3389/fgene.2019.01313. eCollection 2019. Front Genet. 2020. PMID: 32010185 Free PMC article.

2

Hybrid sequencing and map finding (HySeMaFi): optional strategies for extensively deciphering gene splicing and expression in organisms without reference genome.

Ning G, Cheng X, Luo P, Liang F, Wang Z, Yu G, Li X, Wang D, Bao M. Ning G, et al. Among authors: wang z, wang d. Sci Rep. 2017 Mar 8;7:43793. doi: 10.1038/srep43793. Sci Rep. 2017. PMID: 28272530 Free PMC article.

3

Long-read sequence assembly of the firefly Pyrocoelia pectoralis genome.

Fu X, Li J, Tian Y, Quan W, Zhang S, Liu Q, Liang F, Zhu X, Zhang L, Wang D, Hu J. Fu X, et al. Among authors: wang d. Gigascience. 2017 Dec 1;6(12):1-7. doi: 10.1093/gigascience/gix112. Gigascience. 2017. PMID: 29186486 Free PMC article.

4

The N⁶-adenine methylation in yeast genome profiled by single-molecule technology.

Liang Z, Yu G, Liu J, Geng Y, Mao J, Wang D, Zhou J, Gu X. Liang Z, et al. Among authors: wang d. J Genet Genomics. 2018 Apr 20;45(4):223-225. doi: 10.1016/j.jgg.2018.03.003. Epub 2018 Mar 28. J Genet Genomics. 2018. PMID: 29685735 No abstract available.

5

Long-read sequencing identified a causal structural variant in an exome-negative case and enabled preimplantation genetic diagnosis.

Miao H, Zhou J, Yang Q, Liang F, Wang D, Ma N, Gao B, Du J, Lin G, Wang K, Zhang Q. Miao H, et al. Among authors: wang k, wang d. Hereditas. 2018 Sep 28;155:32. doi: 10.1186/s41065-018-0069-1. eCollection 2018. Hereditas. 2018. PMID: 30279644 Free PMC article.

6

DeepSignal: detecting DNA methylation state from Nanopore sequencing reads using deep-learning.

Ni P, Huang N, Zhang Z, Wang DP, Liang F, Miao Y, Xiao CL, Luo F, Wang J. Ni P, et al. Bioinformatics. 2019 Nov 1;35(22):4586-4595. doi: 10.1093/bioinformatics/btz276. Bioinformatics. 2019. PMID: 30994904

7

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: wang k, wang d. Nat Commun. 2019 Jun 4;10(1):2449. doi: 10.1038/s41467-019-10168-2. Nat Commun. 2019. PMID: 31164644 Free PMC article.

8

Long-read sequencing and haplotype linkage analysis enabled preimplantation genetic testing for patients carrying pathogenic inversions.

Zhang S, Liang F, Lei C, Wu J, Fu J, Yang Q, Luo X, Yu G, Wang D, Zhang Y, Lu D, Sun X, Liang Y, Xu C. Zhang S, et al. Among authors: wang d. J Med Genet. 2019 Nov;56(11):741-749. doi: 10.1136/jmedgenet-2018-105976. Epub 2019 Aug 22. J Med Genet. 2019. PMID: 31439719 Free PMC article.

9

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: wang k, wang z, wang d. 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.

10

Nanopore sequencing of African swine fever virus.

Jia L, Jiang M, Wu K, Hu J, Wang Y, Quan W, Hao M, Liu H, Wei H, Fan W, Liu W, Hu R, Wang D, Li J, Chen J, Liu D. Jia L, et al. Among authors: wang y, wang d. Sci China Life Sci. 2020 Jan;63(1):160-164. doi: 10.1007/s11427-019-9828-1. Epub 2019 Nov 5. Sci China Life Sci. 2020. PMID: 31701406 Review. No abstract available.

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