Standout Papers
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data (2010)
- The variant call format and VCFtools (2011)
- A framework for variation discovery and genotyping using next-generation DNA sequencing data (2011)
- From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline (2013)
- Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender (2023)
Immediate Impact
3 by Nobel laureates 56 from Science/Nature 81 standout
Citing Papers
A comprehensive spatio-cellular map of the human hypothalamus
2025 StandoutNature
Refining the impact of genetic evidence on clinical success
2024 StandoutNature
Works of Eric Banks being referenced
Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender
2023 Standout
Evaluating drug targets through human loss-of-function genetic variation
2020
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Eric Banks | 18118 | 17798 | 5181 | 7671 | 29 | 39.1k | |
| Mark A. DePristo | 19141 | 17599 | 5142 | 7767 | 22 | 41.7k | |
| Nils Homer | 23039 | 11288 | 4201 | 8907 | 15 | 40.2k | |
| Kiran Garimella | 14092 | 12020 | 4302 | 4954 | 45 | 29.0k | |
| Robert E. Handsaker | 30572 | 20667 | 5691 | 11996 | 27 | 57.8k | |
| Jue Ruan | 26823 | 12298 | 4326 | 10694 | 64 | 45.0k | |
| Aaron McKenna | 14055 | 10495 | 4826 | 4425 | 26 | 27.8k | |
| Tim Fennell | 26000 | 13949 | 5208 | 9723 | 8 | 45.9k | |
| Andrey Sivachenko | 14768 | 10618 | 4294 | 4456 | 48 | 28.0k | |
| Kristian Cibulskis | 13198 | 10389 | 4695 | 4357 | 21 | 26.7k | |
| Alec Wysoker | 23682 | 11306 | 4209 | 8846 | 9 | 41.7k |
All Works
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