Ashley D. Sanders
Ashley D. Sanders
Adresă de e-mail confirmată pe mdc-berlin.de - Pagina de pornire
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Multi-platform discovery of haplotype-resolved structural variation in human genomes
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Nature communications 10 (1), 1784, 2019
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
A draft human pangenome reference
WW Liao, M Asri, J Ebler, D Doerr, M Haukness, G Hickey, S Lu, JK Lucas, ...
Nature 617 (7960), 312-324, 2023
DNA template strand sequencing of single-cells maps genomic rearrangements at high resolution
E Falconer, M Hills, U Naumann, SSS Poon, EA Chavez, AD Sanders, ...
Nature methods 9 (11), 1107-1112, 2012
Fully phased human genome assembly without parental data using single-cell strand sequencing and long reads
D Porubsky, P Ebert, PA Audano, MR Vollger, WT Harvey, P Marijon, ...
Nature biotechnology 39 (3), 302-308, 2021
The prognostic impact of CD163-positive macrophages in follicular lymphoma: a study from the BC cancer agency and the lymphoma study association
R Kridel, L Xerri, B Gelas-Dore, K Tan, P Feugier, A Vawda, D Canioni, ...
Clinical Cancer Research 21 (15), 3428-3435, 2015
Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads
MR Vollger, GA Logsdon, PA Audano, A Sulovari, D Porubsky, P Peluso, ...
Annals of human genetics 84 (2), 125-140, 2020
Semi-automated assembly of high-quality diploid human reference genomes
ED Jarvis, G Formenti, A Rhie, A Guarracino, C Yang, J Wood, A Tracey, ...
Nature 611 (7936), 519-531, 2022
Single-cell template strand sequencing by Strand-seq enables the characterization of individual homologs
AD Sanders, E Falconer, M Hills, DCJ Spierings, PM Lansdorp
Nature Protocols 12 (6), 1151-1176, 2017
Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility
WC Warren, RA Harris, M Haukness, IT Fiddes, SC Murali, J Fernandes, ...
Science 370 (6523), eabc6617, 2020
Essential role for Ptpn11 in survival of hematopoietic stem and progenitor cells
G Chan, LS Cheung, W Yang, M Milyavsky, AD Sanders, S Gu, WX Hong, ...
Blood, The Journal of the American Society of Hematology 117 (16), 4253-4261, 2011
Human-specific tandem repeat expansion and differential gene expression during primate evolution
A Sulovari, R Li, PA Audano, D Porubsky, MR Vollger, GA Logsdon, ...
Proceedings of the National Academy of Sciences 116 (46), 23243-23253, 2019
Dense and accurate whole-chromosome haplotyping of individual genomes
D Porubsky, S Garg, AD Sanders, JO Korbel, V Guryev, PM Lansdorp, ...
Nature communications 8 (1), 1293, 2017
Characterizing polymorphic inversions in human genomes by single-cell sequencing
AD Sanders, M Hills, D Porubský, V Guryev, E Falconer, PM Lansdorp
Genome research 26 (11), 1575-1587, 2016
Recurrent inversion polymorphisms in humans associate with genetic instability and genomic disorders
D Porubsky, W Höps, H Ashraf, PH Hsieh, B Rodriguez-Martin, F Yilmaz, ...
Cell 185 (11), 1986-2005. e26, 2022
Single-cell analysis of structural variations and complex rearrangements with tri-channel processing
AD Sanders, S Meiers, M Ghareghani, D Porubsky, H Jeong, ...
Nature biotechnology 38 (3), 343-354, 2020
Direct chromosome-length haplotyping by single-cell sequencing
D Porubský, AD Sanders, N Van Wietmarschen, E Falconer, M Hills, ...
Genome research 26 (11), 1565-1574, 2016
Adult spinal cord radial glia display a unique progenitor phenotype
A Petit, AD Sanders, TE Kennedy, W Tetzlaff, KJ Glattfelder, RA Dalley, ...
PloS one 6 (9), e24538, 2011
Recurrent inversion toggling and great ape genome evolution
D Porubsky, AD Sanders, W Höps, PH Hsieh, A Sulovari, R Li, L Mercuri, ...
Nature genetics 52 (8), 849-858, 2020
Familial long-read sequencing increases yield of de novo mutations
MD Noyes, WT Harvey, D Porubsky, A Sulovari, R Li, NR Rose, ...
The American Journal of Human Genetics 109 (4), 631-646, 2022
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