Articles with public access mandates - Wayne E ClarkeLearn more
Available somewhere: 15
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Mandates: US National Institutes of Health, US Department of Veterans Affairs
High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios
M Byrska-Bishop, US Evani, X Zhao, AO Basile, HJ Abel, AA Regier, ...
Cell 185 (18), 3426-3440. e19, 2022
Mandates: US National Institutes of Health, European Molecular Biology Laboratory …
Transcriptome and methylome profiling reveals relics of genome dominance in the mesopolyploid Brassica oleracea
IAP Parkin, C Koh, H Tang, SJ Robinson, S Kagale, WE Clarke, CD Town, ...
Genome biology 15, 1-18, 2014
Mandates: Australian Research Council, Genome Canada, UK Biotechnology and Biological …
Haplotype-resolved diverse human genomes and integrated analysis of structural variation
P Ebert, PA Audano, Q Zhu, B Rodriguez-Martin, D Porubsky, MJ Bonder, ...
Science 372 (6537), eabf7117, 2021
Mandates: US National Institutes of Health, National Natural Science Foundation of …
A high-density SNP genotyping array for Brassica napus and its ancestral diploid species based on optimised selection of single-locus markers in the allotetraploid …
WE Clarke, EE Higgins, J Plieske, R Wieseke, C Sidebottom, Y Khedikar, ...
Theoretical and Applied Genetics 129, 1887-1899, 2016
Mandates: National Natural Science Foundation of China
Curated variation benchmarks for challenging medically relevant autosomal genes
J Wagner, ND Olson, L Harris, J McDaniel, H Cheng, A Fungtammasan, ...
Nature biotechnology 40 (5), 672-680, 2022
Mandates: US National Institutes of Health, US National Aeronautics and Space …
Benchmarking challenging small variants with linked and long reads
J Wagner, ND Olson, L Harris, Z Khan, J Farek, M Mahmoud, A Stankovic, ...
Cell genomics 2 (5), 2022
Mandates: US National Institutes of Health, German Research Foundation, Federal …
Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes
J Ebler, P Ebert, WE Clarke, T Rausch, PA Audano, T Houwaart, Y Mao, ...
Nature genetics 54 (4), 518-525, 2022
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Federal …
Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study
J Foox, SW Tighe, CM Nicolet, JM Zook, M Byrska-Bishop, WE Clarke, ...
Nature biotechnology 39 (9), 1129-1140, 2021
Mandates: Bill & Melinda Gates Foundation, US National Institutes of Health
Genomic DNA enrichment using sequence capture microarrays: a novel approach to discover sequence nucleotide polymorphisms (SNP) in Brassica napus L
WE Clarke, IA Parkin, HA Gajardo, DJ Gerhardt, E Higgins, C Sidebottom, ...
PloS one 8 (12), e81992, 2013
Mandates: Government of Spain
Detecting de Novo Homoeologous Recombination Events in Cultivated Brassica napus Using a Genome-Wide SNP Array
EE Higgins, WE Clarke, EC Howell, SJ Armstrong, IAP Parkin
G3: Genes, Genomes, Genetics 8 (8), 2673-2683, 2018
Mandates: UK Biotechnology and Biological Sciences Research Council
A strategy for building and using a human reference pangenome
B Llamas, G Narzisi, V Schneider, PA Audano, E Biederstedt, L Blauvelt, ...
F1000Research 8, 2019
Mandates: US National Institutes of Health, Australian Research Council, Carlsberg …
A crowdsourced set of curated structural variants for the human genome
LM Chapman, N Spies, P Pai, CS Lim, A Carroll, G Narzisi, CM Watson, ...
PLoS computational biology 16 (6), e1007933, 2020
Mandates: US National Institutes of Health
SVCurator: a crowdsourcing app to visualize evidence of structural variants for the human genome
LM Chapman, N Spies, P Pai, CS Lim, A Carroll, G Narzisi, CM Watson, ...
BioRxiv, 581264, 2019
Mandates: US National Institutes of Health
Multi-Platform Assessment of DNA Sequencing Performance using Human and Bacterial Reference Genomes in the ABRF Next-Generation Sequencing Study
J Foox, SW Tighe, CM Nicolet, JM Zook, M Byrska-Bishop, WE Clarke, ...
bioRxiv, 2020.07. 23.218602, 2020
Mandates: Bill & Melinda Gates Foundation, US National Institutes of Health
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