Results 21 to 30 of about 2,797,849 (300)

Constraints on Variant Axion Models [PDF]

, 1997
A particular class of variant axion models with two higgs doublets and a singlet is studied. In these models the axion couples either to the $u$-quark or $t$-quark or both, but not to $b$, $c$, $s$, or $d$.
A. A. Belavin, A. Burrows, A. P. Zhitnitskii, B. Niczyporuk, C. G. Callan, C. Q. Geng, D. B. Kaplan, G. Edwards, G. G. Raffelt, G. G. Raffelt, G. G. Raffelt, G. Mageras, G. ’t Hooft, H. Leutwyler, J. Bijens, J. E. Kim, J. Kandaswamy, J. Preskill, J. W. Brockway, K. Abe, K. F. Smith, L. M. Krauss, M. A. Shifman, M. Dine, M. S. Salam, M. S. Turner, M. Sivertz, Mark Hindmarsh, P. Sikivie, Photis Moulatsiotis, R. A. Battye, R. Crewther, R. D. Peccei, R. D. Peccei, R. Jackiw, R. Mayle, S. L. Cheng, S. Weinberg, S. Weinberg, V. Baluni, W. A. Bardeen, W. Keil, Y. Asano   +42 more
core   +2 more sources

Step by Step Implementation of Knowledge Sharing for Library In Indonesian

Edulib: Journal of Library and Information Science, 2017
Abstrak. Knowledge sharing banyak diyakini sebagai kegiatan yang mampu mendorong kreativitas dan terciptanya inovasi bagi sebuah organisasi. Banyak organisasi yang memiliki inisiatif menerapkan knowledge sharing demi terciptanya inovasi.
Nove E. Variant Anna
doaj   +1 more source

VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research [PDF]

, 2016
Accurate variant calling in next generation sequencing (NGS) is critical to understand cancer genomes better. Here we present VarDict, a novel and versatile variant caller for both DNA- and RNA-sequencing data.
Ahdesmaki, Miika, Barrett, J. Carl, Chapman, Brad, Dougherty, Brian, Dry, Jonathan R., Hofmann, Oliver, Johnson, Justin, Lai, Zhongwu, Markovets, Aleksandra, McEwen, Robert   +9 more
core   +2 more sources

Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies

Frontiers in Pediatrics, 2021
Background: Epileptic encephalopathies (EEs) are a pediatric entity with highly phenotypic and genetic heterogeneity. Both single nucleotide variants (SNVs)/Indels and copy number variations (CNVs) could be the causes.
Dan Sun, Yan Liu, Wei Cai, Jiehui Ma, Kun Ni, Ming Chen, Cheng Wang, Yongchu Liu, Yuanyuan Zhu, Zhisheng Liu, Feng Zhu, Feng Zhu   +11 more
doaj   +1 more source

Rubredoxin Variant Folds without Iron [PDF]

, 1999
Pyroccocus furiosus rubredoxin (PFRD), like most studied hyperthermophilic proteins, does not undergo reversible folding. The irreversibility of folding is thought to involve PFRD’s iron-binding site.
Mayo, Stephen L., Strop, Pavel
core   +1 more source

Gini Regressions and Heteroskedasticity

Econometrics, 2019
We propose an Aitken estimator for Gini regression. The suggested A-Gini estimator is proven to be a U-statistics. Monte Carlo simulations are provided to deal with heteroskedasticity and to make some comparisons between the generalized least squares ...
Arthur Charpentier, Ndéné Ka, Stéphane Mussard, Oumar Hamady Ndiaye   +3 more
doaj   +1 more source

KERJASAMA DAN JARINGAN PERPUSTAKAAN ANTARA INDONESIA-MALAYSIA INDONESIA-MALAYSIA LIBRARY COOPERATION AND NETWORKING

Edulib: Journal of Library and Information Science, 2015
In the freedom of information age, the openness and easiness of information access is important. The provision of data and information has become crucial for many people. The diversity of the information needs drive many information provider institutions
Dyah Puspitasari, Endang Fitriyah Manan, Nove Variant Anna   +2 more
doaj   +1 more source

EVALUASI PENGGUNA PADA PERPUSTAKAAN DIGITAL UNIVERSITAS AIRLANGGA (UNAIR)

Edulib: Journal of Library and Information Science, 2016
Abstrak Penelitian ini bertujuan untuk mengevaluasi website perpustakaan digital UNAIR yang beralamat di www.lib.unair.ac.id melalui user evaluation teknik.
Dyah Puspitasari Srirahayu, Nove Variant Anna, Ma'isyatus Su'adaa Irfana   +2 more
doaj   +1 more source

Household transmission of COVID-19 cases associated with SARS-CoV-2 delta variant (B.1.617.2): national case-control study

The Lancet Regional Health. Europe, 2022
Summary: Background: The SARS-CoV-2 Delta variant (B.1.617.2), first detected in India, has rapidly become the dominant variant in England. Early reports suggest this variant has an increased growth rate suggesting increased transmissibility. This study
Hester Allen, Amoolya Vusirikala, Joe Flannagan, Katherine A. Twohig, Asad Zaidi, Dimple Chudasama, Theresa Lamagni, Natalie Groves, Charlie Turner, Christopher Rawlinson, Jamie Lopez-Bernal, Ross Harris, Andre Charlett, Gavin Dabrera, Meaghan Kall   +14 more
doaj   +1 more source

CLEVER: Clique-Enumerating Variant Finder [PDF]

, 2012
Next-generation sequencing techniques have facilitated a large scale analysis of human genetic variation. Despite the advances in sequencing speeds, the computational discovery of structural variants is not yet standard.
Bauer, Markus, Canzar, Stefan, Costa, Ivan, Klau, Gunnar, Marschall, Tobias, Schliep, Alexander, Schönhuth, Alexander   +6 more
core   +3 more sources