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Scientific Data|June 9, 2016
Extensive sequencing of seven human genomes to characterize benchmark reference materialsJustin M Zook, David Catoe, Jennifer McDaniel, et al.Nature Biotechnology|July 24, 2020
Author Correction: A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.Nature Biotechnology|June 17, 2020
A robust benchmark for detection of germline large deletions and insertionsJustin M Zook, Nancy F Hansen, Nathan D Olson, et al.Medrxiv : the Preprint Server for Health Sciences|March 18, 2024
Nanopore sequencing of 1000 Genomes Project samples to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.Genome Research|October 2, 2024
High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variationJonas A Gustafson, Sophia B Gibson, Nikhita Damaraju, et al.IEEE Transactions on Medical Imaging|December 11, 2014
The Multimodal Brain Tumor Image Segmentation Benchmark (BRATS)Bjoern H Menze, Andras Jakab, Stefan Bauer, et al.Science (New York, N.Y.)|March 31, 2022
Complete genomic and epigenetic maps of human centromeresNicolas Altemose, Glennis A Logsdon, Andrey V Bzikadze, et al.Cell|August 6, 2026
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.Biorxiv : the Preprint Server for Biology|September 26, 2025
A complete diploid human genome benchmark for personalized genomicsNancy F Hansen, Nathan Dwarshuis, Hyun Joo Ji, et al.Cell Genomics|June 20, 2022
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regionsNathan D Olson, Justin Wagner, Jennifer McDaniel, et al.Pageof 12