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Cell Genomics|December 1, 2022
Benchmarking challenging small variants with linked and long readsJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
F1000Research|August 16, 2021
A strategy for building and using a human reference pangenomeBastien Llamas, Giuseppe Narzisi, Valerie Schneider, et al.
Nature Biotechnology|February 8, 2022
Curated variation benchmarks for challenging medically relevant autosomal genesJustin Wagner, Nathan D Olson, Lindsay Harris, et al.
Cell Genomics|December 20, 2025
Characterization of subclonal variants in HG002 Genome in a Bottle reference material as a resource for benchmarking variant callersCamille A Daniels, Adetola A Abdulkadir, Megan H Cleveland, et al.
Biorxiv : the Preprint Server for Biology|December 16, 2024
A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference materialCamille A Daniels, Adetola Abdulkadir, Megan H Cleveland, et al.
Molecular Therapy. Methods & Clinical Development|July 7, 2025
Interlaboratory assessment of candidate reference materials for lentiviral vector copy number and integration site measurementsHua-Jun He, Zhiyong He, Steven P Lund, et al.
Medical Image Analysis|August 1, 2016
ISLES 2015 - A public evaluation benchmark for ischemic stroke lesion segmentation from multispectral MRIOskar Maier, Bjoern H Menze, Janina von der Gablentz, et al.
Neuroimage|February 6, 2015
Standardized evaluation of algorithms for computer-aided diagnosis of dementia based on structural MRI: the CADDementia challengeEsther E Bron, Marion Smits, Wiesje M van der Flier, et al.
Genome Biology|January 4, 2022
Assessing reproducibility of inherited variants detected with short-read whole genome sequencingBohu Pan, Luyao Ren, Vitor Onuchic, et al.
Biorxiv : the Preprint Server for Biology|December 31, 2025
Complete genomes of a multi-generational pedigree to expand studies of genetic and epigenetic inheritanceMonika Cechova, Tamara A Potapova, Andreas Rechtsteiner, et al.
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