Wang D - Search Results

1

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.

2

Construction of a high-density, high-quality genetic map of cultivated lotus (Nelumbo nucifera) using next-generation sequencing.

Liu Z, Zhu H, Liu Y, Kuang J, Zhou K, Liang F, Liu Z, Wang D, Ke W. Liu Z, et al. Among authors: wang d. BMC Genomics. 2016 Jun 17;17:466. doi: 10.1186/s12864-016-2781-4. BMC Genomics. 2016. PMID: 27317430 Free PMC article.

3

Long-read sequencing and de novo assembly of a Chinese genome.

Shi L, Guo Y, Dong C, Huddleston J, Yang H, Han X, Fu A, Li Q, Li N, Gong S, Lintner KE, Ding Q, Wang Z, Hu J, Wang D, Wang F, Wang L, Lyon GJ, Guan Y, Shen Y, Evgrafov OV, Knowles JA, Thibaud-Nissen F, Schneider V, Yu CY, Zhou L, Eichler EE, So KF, Wang K. Shi L, et al. Among authors: wang f, wang l, wang k, wang z, wang d. Nat Commun. 2016 Jun 30;7:12065. doi: 10.1038/ncomms12065. Nat Commun. 2016. PMID: 27356984 Free PMC article.

4

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.

5

Interrogating the "unsequenceable" genomic trinucleotide repeat disorders by long-read sequencing.

Liu Q, Zhang P, Wang D, Gu W, Wang K. Liu Q, et al. Among authors: wang k, wang d. Genome Med. 2017 Jul 18;9(1):65. doi: 10.1186/s13073-017-0456-7. Genome Med. 2017. PMID: 28720120 Free PMC article.

6

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.

7

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.

8

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. Among authors: wang k, wang d. BMC Bioinformatics. 2018 May 23;19(1):180. doi: 10.1186/s12859-018-2207-1. BMC Bioinformatics. 2018. PMID: 29792160 Free PMC article.

9

N⁶-Methyladenine DNA Modification in the Human Genome.

Xiao CL, Zhu S, He M, Chen D, Zhang Q, Chen Y, Yu G, Liu J, Xie SQ, Luo F, Liang Z, Wang DP, Bo XC, Gu XF, Wang K, Yan GR. Xiao CL, et al. Among authors: wang dp, wang k. Mol Cell. 2018 Jul 19;71(2):306-318.e7. doi: 10.1016/j.molcel.2018.06.015. Epub 2018 Jul 12. Mol Cell. 2018. PMID: 30017583 Free article.

10

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

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