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Institution

Seoul National University

EducationSeoul, South Korea
About: Seoul National University is a education organization based out in Seoul, South Korea. It is known for research contribution in the topics: Population & Catalysis. The organization has 65879 authors who have published 138759 publications receiving 3715170 citations. The organization is also known as: SNU & Seoul-dae.
Topics: Population, Catalysis, Thin film, Gene, Cancer


Papers
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Journal ArticleDOI
TL;DR: Linclust is developed, an algorithm with linear time complexity that can cluster over a billion sequences within hours on a single server, and will help to unlock the great wealth contained in metagenomic and genomic sequence databases.
Abstract: Metagenomic datasets contain billions of protein sequences that could greatly enhance large-scale functional annotation and structure prediction. Utilizing this enormous resource would require reducing its redundancy by similarity clustering. However, clustering hundreds of millions of sequences is impractical using current algorithms because their runtimes scale as the input set size N times the number of clusters K, which is typically of similar order as N, resulting in runtimes that increase almost quadratically with N. We developed Linclust, the first clustering algorithm whose runtime scales as N, independent of K. It can also cluster datasets several times larger than the available main memory. We cluster 1.6 billion metagenomic sequence fragments in 10 h on a single server to 50% sequence identity, >1000 times faster than has been possible before. Linclust will help to unlock the great wealth contained in metagenomic and genomic sequence databases. Billions of metagenomic and genomic sequences fill up public datasets, which makes similarity clustering an important and time-critical analysis step. Here, the authors develop Linclust, an algorithm with linear time complexity that can cluster over a billion sequences within hours on a single server.

448 citations

Journal ArticleDOI
TL;DR: In this paper, a simple heat treatment of a mixture composed of tin(IV) tetrachloride pentahydrate (SnCl4·5H2O) and resorcinol-formaldehyde gel (RF gel) was used to synthesize hollow tin dioxide (SnO2) microspheres.
Abstract: Hollow tin dioxide (SnO2) microspheres were synthesized by the simple heat treatment of a mixture composed of tin(IV) tetrachloride pentahydrate (SnCl4·5H2O) and resorcinol–formaldehyde gel (RF gel). Because hollow structures were formed during the heat treatment, the pre-formation of template and the adsorption of target precursor on template are unnecessary in the current method, leading to simplified synthetic procedures and facilitating mass production. Field-emission scanning electron microscopy (FE-SEM) images showed 1.7–2.5 μm sized hollow spherical particles. Transmission electron microscopy (TEM) images showed that the produced spherical particles are composed of a hollow inner cavity and thin outer shell. When the hollow SnO2 microspheres were used as a lithium-battery anode, they exhibited extraordinarily high discharge capacities and coulombic efficiency. The reported synthetic procedure is straightforward and inexpensive, and consequently can be readily adopted to produce large quantities of hollow SnO2 microspheres. This straightforward approach can be extended for the synthesis of other hollow microspheres including those obtained from ZrO2 and ZrO2/CeO2 solid solutions.

448 citations

Journal ArticleDOI
TL;DR: Addition of lapatinib to CapeOx did not increase OS in patients with HER2-amplified gastroesophageal adenocarcinoma, and no correlation was observed between HER2 immunohistochemistry status and survival.
Abstract: PurposeTo evaluate the efficacy of adding lapatinib to capecitabine and oxaliplatin (CapeOx) in patients with previously untreated human epidermal growth factor receptor 2 (HER2) –amplified advanced gastroesophageal adenocarcinoma.Patients and MethodsPatients with HER2-positive advanced gastroesophageal adenocarcinoma were randomly assigned at a one-to-one ratio to CapeOx plus lapatinib 1,250 mg or placebo daily. Primary end point was overall survival (OS) in patients with centrally confirmed HER2 amplification in the primary efficacy population.ResultsA total of 545 patients were randomly assigned, and 487 patients comprised the primary efficacy population. Median OS in the lapatinib and placebo arms was 12.2 (95% CI, 10.6 to 14.2) and 10.5 months (95% CI, 9.0 to 11.3), respectively, which was not significantly different (hazard ratio, 0.91; 95% CI, 0.73 to 1.12). Median progression-free survival in the lapatinib and placebo arms was 6.0 (95% CI, 5.6 to 7.0) and 5.4 months (95% CI, 4.4 to 5.7), respectiv...

448 citations

Journal ArticleDOI
TL;DR: SOC1, encoding a MADS box transcription factor, integrates multiple flowering signals derived from photoperiod, temperature, hormone, and age-related signals, and is regulated by two antagonistic flowering regulators, CONSTANS and FLOWERING LOCUS C (FLC), which act as floral activator and repressor, respectively.
Abstract: SOC1, encoding a MADS box transcription factor, integrates multiple flowering signals derived from photoperiod, temperature, hormone, and age-related signals. SOC1 is regulated by two antagonistic flowering regulators, CONSTANS (CO) and FLOWERING LOCUS C (FLC), which act as floral activator and repressor, respectively. CO activates SOC1 mainly through FT but FLC represses SOC1 by direct binding to the promoter. SOC1 is also activated by an age-dependent mechanism in which SPL9 and microRNA156 are involved. When SOC1 is induced at the shoot apex, SOC1 together with AGL24 directly activates LEAFY (LFY), a floral meristem identity gene. APETALA1 (AP1), activated mainly by FT, is also necessary to establish and maintain flower meristem identity. When LFY and AP1 are established, flower development occurs at the anlagen of shoot apical meristem according to the ABC model. During early flower development, AP1 activates the A function and represses three redundantly functioning flowering time genes, SOC1, AGL24, and SVP to prevent floral reversion. During late flower development, such repression is also necessary to activate SEPALATA3 (SEP3) which is a coactivator of B and C function genes with LFY, otherwise SEP3 is suppressed by SOC1, AGL24, and SVP. Therefore, SOC1 is necessary to prevent premature differentiation of the floral meristem.

448 citations

Journal ArticleDOI
TL;DR: A mechanism for irreversible degradation of perovskite materials in which trapped charges, regardless of the polarity, play a decisive role is uncovered.
Abstract: Perovskite solar cells have shown unprecedent performance increase up to 22% efficiency. However, their photovoltaic performance has shown fast deterioration under light illumination in the presence of humid air even with encapulation. The stability of perovskite materials has been unsolved and its mechanism has been elusive. Here we uncover a mechanism for irreversible degradation of perovskite materials in which trapped charges, regardless of the polarity, play a decisive role. An experimental setup using different polarity ions revealed that the moisture-induced irreversible dissociation of perovskite materials is triggered by charges trapped along grain boundaries. We also identified the synergetic effect of oxygen on the process of moisture-induced degradation. The deprotonation of organic cations by trapped charge-induced local electric field would be attributed to the initiation of irreversible decomposition.

447 citations


Authors

Showing all 66324 results

NameH-indexPapersCitations
Hyun-Chul Kim1764076183227
Adi F. Gazdar157776104116
Alfred L. Goldberg15647488296
Yongsun Kim1562588145619
David J. Mooney15669594172
Roberto Romero1511516108321
Jongmin Lee1502257134772
Byung-Sik Hong1461557105696
Inkyu Park1441767109433
Teruki Kamon1422034115633
John L. Hopper140122986392
Ali Khademhosseini14088776430
Taeghwan Hyeon13956375814
Suyong Choi135149597053
Intae Yu134137289870
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023241
2022768
20218,297
20208,368
20198,175
20187,617