A citation-based method for searching scientific literature

Brett Trost, Susan Walker, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Jeffrey R MacDonald, Wilson W L Sung, Sergio L Pereira, Joe Whitney, Ada J S Chan, Giovanna Pellecchia, Miriam S Reuter, Si Lok, Ryan K C Yuen, Christian R Marshall, Daniele Merico, Stephen W Scherer. Am J Hum Genet 2018
Times Cited: 74



Mehdi Pirooznia, Fernando S Goes, Peter P Zandi. Front Genet 2015
Times Cited: 80




List of shared articles



Times cited

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese, David M Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld,[...]. Genome Med 2021
5

CNVfilteR: an R/bioconductor package to identify false positives produced by germline NGS CNV detection tools.
José Marcos Moreno-Cabrera, Jesús Del Valle, Elisabeth Castellanos, Lidia Feliubadaló, Marta Pineda, Eduard Serra, Gabriel Capellá, Conxi Lázaro, Bernat Gel. Bioinformatics 2021
0

A random forest-based framework for genotyping and accuracy assessment of copy number variations.
Xuehan Zhuang, Rui Ye, Man-Ting So, Wai-Yee Lam, Anwarul Karim, Michelle Yu, Ngoc Diem Ngo, Stacey S Cherny, Paul Kwong-Hang Tam, Maria-Mercè Garcia-Barcelo,[...]. NAR Genom Bioinform 2020
2

4

Evaluation of tools for identifying large copy number variations from ultra-low-coverage whole-genome sequencing data.
Johannes Smolander, Sofia Khan, Kalaimathy Singaravelu, Leni Kauko, Riikka J Lund, Asta Laiho, Laura L Elo. BMC Genomics 2021
0

WisecondorX: improved copy number detection for routine shallow whole-genome sequencing.
Lennart Raman, Annelies Dheedene, Matthias De Smet, Jo Van Dorpe, Björn Menten. Nucleic Acids Res 2019
24

Copy-number variation in goat genome sequence: A comparative analysis of the different litter size trait groups.
Rui-Qian Zhang, Jun-Jie Wang, Teng Zhang, Hong-Li Zhai, Wei Shen. Gene 2019
9