نتایج جستجو برای: and ngs r 0950 p

تعداد نتایج: 17047258  

Journal: :Information & Software Technology 2014
José Matías Rivero Julián Grigera Gustavo Rossi Esteban Robles Luna Francisco Montero Simarro Martin Gaedke

http://dx.doi.org/10.1016/j.infsof.2014.01.011 0950-5849/ 2014 Elsevier B.V. All rights reserved. ⇑ Corresponding author at: LIFIA, Facultad de Informática, UNLP, Calle 50 y 120, La Plata, Buenos Aires, Argentina. Tel.: +54 92215082703. E-mail addresses: [email protected] (J.M. Rivero), julian.grigera@ lifia.info.unlp.edu.ar (J. Grigera), [email protected] (G. Rossi), ...

Journal: :Information & Software Technology 2014
Ivan do Carmo Machado John D. McGregor Yguaratã Cerqueira Cavalcanti Eduardo Santana de Almeida

http://dx.doi.org/10.1016/j.infsof.2014.04.002 0950-5849/ 2014 Elsevier B.V. All rights reserved. ⇑ Corresponding author. Tel.: +55 71 9183 9735. E-mail addresses: [email protected] (I.d.C. Machado), [email protected] (J.D. McGregor), [email protected] (Y.C. Cavalcanti), [email protected] Almeida). Ivan do Carmo Machado a,⇑, John D. McGregor , Yguaratã Cerqueira Cavalcanti , Eduardo Santa...

Journal: :Information & Software Technology 2014
Laura García-Borgoñón M. A. Barcelona J. A. García-García M. Alba María José Escalona Cuaresma

0950-5849/$ see front matter 2013 Elsevier B.V. All rights reserved. http://dx.doi.org/10.1016/j.infsof.2013.10.001 ⇑ Corresponding author. Tel.: + 34 954552852; fax: + 34 954556817. E-mail addresses: [email protected] (L. García-Borgoñón), [email protected] (M.A. Barcelona), [email protected] (J.A. García-García), [email protected] (M. Alba), [email protected] (M.J. Escalona). L. García-Bo...

2013
Satoshi Narumi Kumihiro Matsuo Tomohiro Ishii Yusuke Tanahashi Tomonobu Hasegawa

Somatic activating GNAS mutations cause McCune-Albright syndrome (MAS). Owing to low mutation abundance, mutant-specific enrichment procedures, such as the peptide nucleic acid (PNA) method, are required to detect mutations in peripheral blood. Next generation sequencing (NGS) can analyze millions of PCR amplicons independently, thus it is expected to detect low-abundance GNAS mutations quantit...

Journal: :Journal of Topology 2022

In this paper, we study the elliptic spectral sequence computing $tmf_*(\mathbb{R} P^2)$ and $tmf_* (\mathbb{R} P^2 \wedge \mathbb{C} P^2)$. Specifically, compute all differentials resolve exotic extensions by 2, $\eta$, $\nu$. For P^2)$, also effect of $v_1$-self maps $\mathbb{R} P^2$ on $tmf$-homology.

2017
Seok Joong Yun Seon-Kyu Kim Jayoung Kim Eun-Jong Cha Jang-Seong Kim Sun-Jin Kim Yun-Sok Ha Ye-Hwan Kim Pildu Jeong Ho Won Kang Jeong-Hwan Kim Jong-Lyul Park Young-Ki Choi Sung-Kwon Moon Yung-Hyun Choi Seon-Young Kim Wun-Jae Kim

Although various mechanisms of castration-resistant prostate cancer (CRPC) have been discovered, reliable biomarkers for monitoring CRPC progression are lacking. We sought to identify molecules that predict the progression of advanced prostate cancer (AdvPC) into CRPC. The study used primary-site samples (N=45 for next-generation sequencing (NGS); N=243 for real-time polymerase chain reaction) ...

2005
K. P. STRICKLAND

Dawson, R. M. C. (1955). In Biochemistry of the Developing Nervous System, p. 268. Ed. by Waelsch, H. New York: Academic Press Inc. Ernster, L., Zetterstrom, R. & Lindberg, 0. (1950). Acta chem. scand. 4, 942. Folch, J., Lees, M. & Sloane-Stanley, G. H. (1957). J. biol. Chem. 226, 497. Hanahan, D. J. (1954a). J. biol. Chem. 211, 313. Hanahan, D. J. (1954b). J. biol. Chem. 211, 321. Hanahan, D. ...

2004
William Gasarch

Alice wants to query a database but she does not want the database to learn what she is querying. She can ask for the entire database. Can she get her query answered with less communication? One model of this problem is Private Information Retrieval, henceforth PIR. We survey results obtained about the PIR model including partial answers to the following questions. (1) What if there are k non-c...

2011
H. Johansson M. Isaksson E. Falk Sörqvist F. Roos Johan Stenberg T. Sjöblom J. Botling P. Micke K. Edlund S. Fredriksson H. Göransson Kultima Olle Ericsson Mats Nilsson

Targeted genome enrichment is a powerful tool for making use of the massive throughput of novel DNA-sequencing instruments. We herein present a simple and scalable protocol for multiplex amplification of target regions based on the Selector technique. The updated version exhibits improved coverage and compatibility with next-generation-sequencing (NGS) library-construction procedures for shotgu...

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