オープン アクセスを義務付けられた論文 - Adam English詳細
一般公開: 23 件
Mind the gap: upgrading genomes with Pacific Biosciences RS long-read sequencing technology
AC English, S Richards, Y Han, M Wang, V Vee, J Qu, X Qin, DM Muzny, ...
PloS one 7 (11), e47768, 2012
委任: US National Institutes of Health
The somatic genomic landscape of chromophobe renal cell carcinoma
CF Davis, CJ Ricketts, M Wang, L Yang, AD Cherniack, H Shen, C Buhay, ...
Cancer cell 26 (3), 319-330, 2014
委任: US National Institutes of Health
Finding the missing honey bee genes: lessons learned from a genome upgrade
CG Elsik, KC Worley, AK Bennett, M Beye, F Camara, CP Childers, ...
BMC genomics 15, 1-29, 2014
委任: US Department of Energy, US National Institutes of Health
A robust benchmark for detection of germline large deletions and insertions
JM Zook, NF Hansen, ND Olson, L Chapman, JC Mullikin, C Xiao, ...
Nature biotechnology 38 (11), 1347-1355, 2020
委任: US National Science Foundation, US Department of Energy, US National …
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
JG Reid, A Carroll, N Veeraraghavan, M Dahdouli, A Sundquist, A English, ...
BMC bioinformatics 15, 1-11, 2014
委任: US National Institutes of Health
Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
AA Regier, Y Farjoun, DE Larson, O Krasheninina, HM Kang, ...
Nature communications 9 (1), 4038, 2018
委任: US National Institutes of Health
Assessing structural variation in a personal genome—towards a human reference diploid genome
AC English, WJ Salerno, OA Hampton, C Gonzaga-Jauregui, S Ambreth, ...
BMC genomics 16, 1-15, 2015
委任: US National Institutes of Health, Howard Hughes Medical Institute, Damon …
Truvari: refined structural variant comparison preserves allelic diversity
AC English, VK Menon, RA Gibbs, GA Metcalf, FJ Sedlazeck
Genome Biology 23 (1), 271, 2022
委任: US National Institutes of Health
Sooty mangabey genome sequence provides insight into AIDS resistance in a natural SIV host
D Palesch, SE Bosinger, GK Tharp, TH Vanderford, M Paiardini, ...
Nature 553 (7686), 77-81, 2018
委任: US National Institutes of Health, German Research Foundation, European …
PacBio-LITS: a large-insert targeted sequencing method for characterization of human disease-associated chromosomal structural variations
M Wang, CR Beck, AC English, Q Meng, C Buhay, Y Han, ...
BMC genomics 16, 1-12, 2015
委任: US National Institutes of Health, Howard Hughes Medical Institute, Damon …
Megabase length hypermutation accompanies human structural variation at 17p11. 2
CR Beck, CMB Carvalho, ZC Akdemir, FJ Sedlazeck, X Song, Q Meng, ...
Cell 176 (6), 1310-1324. e10, 2019
委任: US National Institutes of Health, Howard Hughes Medical Institute, Damon …
Improved annotation of the insect vector of citrus greening disease: biocuration by a diverse genomics community
S Saha, PS Hosmani, K Villalobos-Ayala, S Miller, T Shippy, M Flores, ...
Database 2017, bax032, 2017
委任: US Department of Energy, US National Institutes of Health, US Department of …
A robust benchmark for germline structural variant detection
JM Zook, NF Hansen, ND Olson, LM Chapman, JC Mullikin, C Xiao, ...
BioRxiv, 664623, 2019
委任: US National Institutes of Health
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease
X Zhang, C Zhu, G Beecham, BN Vardarajan, Y Ma, D Lancour, JJ Farrell, ...
Alzheimer's & Dementia 15 (3), 441-452, 2019
委任: US National Institutes of Health
xAtlas: scalable small variant calling across heterogeneous next-generation sequencing experiments
J Farek, D Hughes, W Salerno, Y Zhu, A Pisupati, A Mansfield, ...
GigaScience 12, giac125, 2023
委任: US National Institutes of Health
Human genome meeting 2016: Houston, TX, USA. 28 February-2 March 2016
AK Srivastava, Y Wang, R Huang, C Skinner, T Thompson, L Pollard, ...
Human genomics 10, 1-40, 2016
委任: US National Institutes of Health, Chinese Academy of Sciences
Structural variation across 138,134 samples in the TOPMed consortium
G Jun, AC English, GA Metcalf, J Yang, MJP Chaisson, N Pankratz, ...
Research square, rs. 3. rs-2515453, 2023
委任: US National Institutes of Health, National Health and Medical Research …
Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms
S Behera, S Catreux, M Rossi, S Truong, Z Huang, M Ruehle, A Visvanath, ...
BioRxiv, 2024
委任: US National Institutes of Health
SVachra: a tool to identify genomic structural variation in mate pair sequencing data containing inward and outward facing reads
OA Hampton, AC English, M Wang, WJ Salerno, Y Liu, DM Muzny, Y Han, ...
BMC genomics 18, 31-36, 2017
委任: US National Institutes of Health
muCNV: genotyping structural variants for population-level sequencing
G Jun, F Sedlazeck, Q Zhu, A English, G Metcalf, HM Kang, ...
Bioinformatics 37 (14), 2055-2057, 2021
委任: US National Institutes of Health
公開と助成金に関する情報は、コンピュータ プログラムによって自動的に決定されます