Andy Wing Chun Pang
Andy Wing Chun Pang
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The diploid genome sequence of an individual human
S Levy, G Sutton, PC Ng, L Feuk, AL Halpern, BP Walenz, N Axelrod, ...
PLoS biology 5 (10), e254, 2007
Origins and functional impact of copy number variation in the human genome
DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ...
Nature 464 (7289), 704-712, 2010
Assembly and diploid architecture of an individual human genome via single-molecule technologies
Nature Methods 12 (8), 780-786, 2015
Multi-platform discovery of haplotype-resolved structural variation in human genomes
Nature Communications, 2019
The axolotl genome and the evolution of key tissue formation regulators
S Nowoshilow, S Schloissnig, JF Fei, A Dahl, AWC Pang, M Pippel, ...
Nature 554 (7690), 50-55, 2018
Towards a comprehensive structural variation map of an individual human genome
AW Pang, JR MacDonald, D Pinto, J Wei, MA Rafiq, DF Conrad, H Park, ...
High-resolution comparative analysis of great ape genomes
ZN Kronenberg, IT Fiddes, D Gordon, S Murali, S Cantsilieris, ...
Science 360 (6393), 2018
Genome-Wide Structural Variation Detection by Genome Mapping on Nanochannel Arrays
Genetics 202 (1), 351362, 2016
Whole Genome Mutational Burden Analysis of Three Pluripotency Induction Methods
K Bhutani, K Nazor, R Williams, H Tran, H Dai, Z Dzakula, E Cho, ...
Nature Communications, 2016
Combination of short-read, long-read, and optical mapping assemblies reveals large-scale tandem repeat arrays with population genetic implications
MH Weissensteiner, AWC Pang, I Bunikis, I Hijer, O Vinnere-Petterson, ...
Genome research 27 (5), 697-708, 2017
Mechanisms of formation of structural variation in a fully sequenced human genome
AWC Pang, O Migita, JR MacDonald, L Feuk, SW Scherer
Human mutation 34 (2), 345-354, 2013
SIMPROT: using an empirically determined indel distribution in simulations of protein evolution
A Pang, AD Smith, PAS Nuin, ERM Tillier
BMC bioinformatics 6 (1), 1-7, 2005
Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle
WY Low, R Tearle, R Liu, S Koren, A Rhie, DM Bickhart, BD Rosen, ...
Nature communications 11 (1), 1-14, 2020
Performance of high-throughput sequencing for the discovery of genetic variation across the complete size spectrum
AWC Pang, JR MacDonald, RKC Yuen, VM Hayes, SW Scherer
G3: Genes, Genomes, Genetics 4 (1), 63-65, 2014
Positional homology in bacterial genomes
IJ Burgetz, S Shariff, A Pang, ERM Tillier*
Evolutionary Bioinformatics 2, 117693430600200031, 2006
Comparative analysis of genome tiling array data reveals many novel primate-specific functional RNAs in human
Z Zhang, AWC Pang, M Gerstein
BMC Evolutionary Biology 7 (1), 1-12, 2007
Rapid automated large structural variation detection in a diploid genome by nanochannel based next-generation mapping
AR Hastie, ET Lam, AWC Pang, X Zhang, W Andrews, J Lee, TY Liang, ...
BioRxiv, 102764, 2017
Multi-platform discovery of haplotype-resolved structural variation in human genomes. Nat Commun. 2019; 10 (1): 1784
MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ...
Epub 2019/04/18. https://doi. org/10.1038/s41467-018-08148-z PMID: 30992455, 0
Identification of somatic structural variants in solid tumors by optical genome mapping
D Y Goldrich, B LaBarge, S Chartrand, L Zhang, HB Sadowski, Y Zhang, ...
Journal of Personalized Medicine 11 (2), 142, 2021
Genomic inversions and GOLGA core duplicons underlie disease instability at the 15q25 locus
FAM Maggiolini, S Cantsilieris, P D’Addabbo, M Manganelli, BP Coe, ...
PLoS genetics 15 (3), e1008075, 2019
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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