A citation-based method for searching scientific literature

Ken Chen, John W Wallis, Michael D McLellan, David E Larson, Joelle M Kalicki, Craig S Pohl, Sean D McGrath, Michael C Wendl, Qunyuan Zhang, Devin P Locke, Xiaoqi Shi, Robert S Fulton, Timothy J Ley, Richard K Wilson, Li Ding, Elaine R Mardis. Nat Methods 2009
Times Cited: 931



Daniel L Cameron, Jan Schröder, Jocelyn Sietsma Penington, Hongdo Do, Ramyar Molania, Alexander Dobrovic, Terence P Speed, Anthony T Papenfuss. Genome Res 2017
Times Cited: 120




List of shared articles



Times cited

Robust Benchmark Structural Variant Calls of An Asian Using State-of-the-art Long-read Sequencing Technologies.
Xiao Du, Lili Li, Fan Liang, Sanyang Liu, Wenxin Zhang, Shuai Sun, Yuhui Sun, Fei Fan, Linying Wang, Xinming Liang,[...]. Genomics Proteomics Bioinformatics 2022
2

Mako: A Graph-based Pattern Growth Approach to Detect Complex Structural Variants.
Jiadong Lin, Xiaofei Yang, Walter Kosters, Tun Xu, Yanyan Jia, Songbo Wang, Qihui Zhu, Mallory Ryan, Li Guo, Chengsheng Zhang,[...]. Genomics Proteomics Bioinformatics 2022
2

Progress in Methods for Copy Number Variation Profiling.
Veronika Gordeeva, Elena Sharova, Georgij Arapidi. Int J Mol Sci 2022
2

A Practical Guide to Using Structural Variants for Genome-Wide Association Studies.
Marc-André Lemay, Sidiki Malle. Methods Mol Biol 2022
0

Expanding the conservation genomics toolbox: Incorporating structural variants to enhance genomic studies for species of conservation concern.
Jana Wold, Klaus-Peter Koepfli, Stephanie J Galla, David Eccles, Carolyn J Hogg, Marissa F Le Lec, Joseph Guhlin, Anna W Santure, Tammy E Steeves. Mol Ecol 2021
5

Detection of somatic structural variants from short-read next-generation sequencing data.
Tingting Gong, Vanessa M Hayes, Eva K F Chan. Brief Bioinform 2021
13

Detecting Causal Variants in Mendelian Disorders Using Whole-Genome Sequencing.
Abdul Rezzak Hamzeh, T Daniel Andrews, Matt A Field. Methods Mol Biol 2021
1