Samantha Zarate - Concepedia

Author

Samantha Zarate

DNAnexus (United States)ORCID

Also Known As

Evan Edelstein, Olga Krasheninina, S E Cárdenas Zárate, S.E. Cárdenas Zárate, Samantha Zarate, Zarate, Samantha

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

DNAnexus (United States)Baylor College of Medicine Johns Hopkins University University of California, Santa Cruz National Center for Biotechnology Information

About

Samantha Zarate is an author at DNAnexus (United States) specializing in genetics, genomics, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.3K
2	Engineering	3	3	214
3	Public Health	2	2	488
4	Biostatistics	2	2	467
5	Natural Sciences	1	1	42

Samantha Zarate

Publications

Citations

H-Index

Page 1

	Year	Citations
The complete sequence of a human genome Sergey Nurk, Sergey Koren, Arang Rhie, Science	2022	3.1K
The complete sequence of a human Y chromosome Arang Rhie, Sergey Nurk, Monika Čechová, Nature Human Y ChromosomeChromatinCytogeneticsGeneticsChromosome Biology	2023	415
A complete reference genome improves analysis of human genetic variation Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, Science GeneticsGenetic EpidemiologyGenomicsHuman VariationRead Mapping	2022	407
Benchmarking challenging small variants with linked and long reads Justin Wagner, Nathan D. Olson, Lindsay Harris, Cell Genomics	2022	195
The complete sequence of a human genome Sergey Nurk, Sergey Koren, Arang Rhie, ChromatinFunctional GenomicsCelera GenomicsGeneticsChromosome 22	2021	180
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space Michael C. Schatz, Anthony Philippakis, Enis Afgan, Cell Genomics EngineeringBiological DatabaseData ScienceInformatics Lab-spaceBioinformatics Database	2022	126
Parliament2: Accurate structural variant calling at scale Samantha Zarate, Andrew Carroll, Medhat Mahmoud, GigaScience	2020	103
A diploid assembly-based benchmark for variants in the major histocompatibility complex Chen-Shan Chin, Justin Wagner, Qiandong Zeng, Nature Communications	2020	97
A complete reference genome improves analysis of human genetic variation Sergey Aganezov, Stephanie M. Yan, Daniela C. Soto, GeneticsGenomicsGenetic MedicineClinical GeneticsHuman Phenotypes	2021	81
Benchmarking challenging small variants with linked and long reads Justin Wagner, Nathan D. Olson, Lindsay Harris, EngineeringGeneticsComputer ArchitectureNew BenchmarkGenomics	2020	60

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