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)
- A guide to deep learning in healthcare (2018)
- A universal SNP and small-indel variant caller using deep neural networks (2018)
- Simultaneous determination of protein structure and dynamics (2005)
- Using deep learning to annotate the protein universe (2022)
Immediate Impact
4 by Nobel laureates 54 from Science/Nature 82 standout
Citing Papers
Artificial intelligence and illusions of understanding in scientific research
2024 StandoutNature
All-analog photoelectronic chip for high-speed vision tasks
2023 StandoutNature
Works of Mark A. DePristo being referenced
Using deep learning to annotate the protein universe
2022 Standout
A guide to deep learning in healthcare
2018 Standout
Author Peers
| Author | Last Decade | Papers | Cites | ||||
|---|---|---|---|---|---|---|---|
| Mark A. DePristo | 19141 | 17599 | 521 | 7767 | 22 | 41.7k | |
| Eric Banks | 18118 | 17798 | 30 | 7671 | 29 | 39.1k | |
| Nils Homer | 23039 | 11288 | 91 | 8907 | 15 | 40.2k | |
| Robert E. Handsaker | 30572 | 20667 | 103 | 11996 | 27 | 57.8k | |
| Tim Fennell | 26000 | 13949 | 95 | 9723 | 8 | 45.9k | |
| Alec Wysoker | 23682 | 11306 | 93 | 8846 | 9 | 41.7k | |
| Kiran Garimella | 14092 | 12020 | 28 | 4954 | 45 | 29.0k | |
| Aaron McKenna | 14055 | 10495 | 27 | 4425 | 26 | 27.8k | |
| Jue Ruan | 26823 | 12298 | 107 | 10694 | 64 | 45.0k | |
| Kristian Cibulskis | 13198 | 10389 | 22 | 4357 | 21 | 26.7k | |
| Geo Pertea | 28596 | 6691 | 178 | 13359 | 27 | 46.7k |
All Works
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