A citation-based method for searching scientific literature

Aaron M Wenger, Paul Peluso, William J Rowell, Pi-Chuan Chang, Richard J Hall, Gregory T Concepcion, Jana Ebler, Arkarachai Fungtammasan, Alexey Kolesnikov, Nathan D Olson, Armin Töpfer, Michael Alonge, Medhat Mahmoud, Yufeng Qian, Chen-Shan Chin, Adam M Phillippy, Michael C Schatz, Gene Myers, Mark A DePristo, Jue Ruan, Tobias Marschall, Fritz J Sedlazeck, Justin M Zook, Heng Li, Sergey Koren, Andrew Carroll, David R Rank, Michael W Hunkapiller. Nat Biotechnol 2019
Times Cited: 241



Mark J P Chaisson, John Huddleston, Megan Y Dennis, Peter H Sudmant, Maika Malig, Fereydoun Hormozdiari, Francesca Antonacci, Urvashi Surti, Richard Sandstrom, Matthew Boitano, Jane M Landolin, John A Stamatoyannopoulos, Michael W Hunkapiller, Jonas Korlach, Evan E Eichler. Nature 2015
Times Cited: 386




List of shared articles



Times cited

Identifying the causes and consequences of assembly gaps using a multiplatform genome assembly of a bird-of-paradise.
Valentina Peona, Mozes P K Blom, Luohao Xu, Reto Burri, Shawn Sullivan, Ignas Bunikis, Ivan Liachko, Tri Haryoko, Knud A Jønsson, Qi Zhou,[...]. Mol Ecol Resour 2021
17

Finding long tandem repeats in long noisy reads.
Shinichi Morishita, Kazuki Ichikawa, Eugene W Myers. Bioinformatics 2021
0

Long-read trio sequencing of individuals with unsolved intellectual disability.
Marc Pauper, Erdi Kucuk, Aaron M Wenger, Shreyasee Chakraborty, Primo Baybayan, Michael Kwint, Bart van der Sanden, Marcel R Nelen, Ronny Derks, Han G Brunner,[...]. Eur J Hum Genet 2021
2

Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads.
David Porubsky, Peter Ebert, Peter A Audano, Mitchell R Vollger, William T Harvey, Pierre Marijon, Jana Ebler, Katherine M Munson, Melanie Sorensen, Arvis Sulovari,[...]. Nat Biotechnol 2021
18

The changing face of genome assemblies: Guidance on achieving high-quality reference genomes.
Annabel Whibley, Joanna L Kelley, Shawn R Narum. Mol Ecol Resour 2021
7


Applying genomic and transcriptomic advances to mitochondrial medicine.
William L Macken, Jana Vandrovcova, Michael G Hanna, Robert D S Pitceathly. Nat Rev Neurol 2021
3

Haplotype-resolved diverse human genomes and integrated analysis of structural variation.
Peter Ebert, Peter A Audano, Qihui Zhu, Bernardo Rodriguez-Martin, David Porubsky, Marc Jan Bonder, Arvis Sulovari, Jana Ebler, Weichen Zhou, Rebecca Serra Mari,[...]. Science 2021
32

A comprehensive review of scaffolding methods in genome assembly.
Junwei Luo, Yawei Wei, Mengna Lyu, Zhengjiang Wu, Xiaoyan Liu, Huimin Luo, Chaokun Yan. Brief Bioinform 2021
1

Genetic basis of mitochondrial diseases.
Mirjana Gusic, Holger Prokisch. FEBS Lett 2021
5


Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences.
Marzieh Eslami Rasekh, Yözen Hernández, Samantha D Drinan, Juan I Fuxman Bass, Gary Benson. Nucleic Acids Res 2021
0