scispace - formally typeset
Search or ask a question
Institution

University of Oviedo

EducationOviedo, Spain
About: University of Oviedo is a education organization based out in Oviedo, Spain. It is known for research contribution in the topics: Population & Catalysis. The organization has 13423 authors who have published 31649 publications receiving 844799 citations. The organization is also known as: Universidá d'Uviéu & Universidad de Oviedo.


Papers
More filters
Journal ArticleDOI
TL;DR: Investigation of in situ bioremediation of polluted soils with diesel fuel with microbiological and chemical analyses and a suitable bioreactor design suggested the best ways to improve biodegradation extents in a diesel-enriched soil.
Abstract: The development of a simple laboratory methodology allows theimplementation of in situbioremediation of polluted soils with diesel fuel. In thisinvestigation microbiological and chemical analyses and a suitable bioreactor design, were veryuseful for suggesting the best ways to improve biodegradation extents in a diesel-enrichedsoil. Biostimulation with inorganic nitrogen and phosphorus produced the best resultsin a simple bioreactor, with biodegradation extents higher than 90% after 45 days. Also,the addition of activated sludge from a domestic wastewater plant increased the degradationrate to a great extent. In both cases, microbiological studies showed the presence ofAcinetobacter sp. degrading most of thehydrocarbons. Simultaneously, a diesel fuel release(approximately 400,000 l) was studied. Samples taken in polluted soil and water revealed thatbacteria from the genus Acinetobacterwere predominant. In plate studies, Acinetobacter coloniesproduced a whitish substance with the characteristics of a biosurfactant. Remarkably, thepresence of this product was evident at the field site, both in the riverbanks and in the physicalrecovery plant. The study of the similarities between laboratory results and the diesel spillsite strongly suggested that natural conditions at the field site allowed the implementationof in situ bioremediation after physical removal of LNAPL (light nonaqueous-phase liquids).

279 citations

Journal ArticleDOI
07 May 2010-Science
TL;DR: It is shown that hybridization capture on microarrays can successfully recover more than a megabase of target regions from Neandertal DNA even in the presence of ~99.8% microbial DNA.
Abstract: Neandertals, our closest relatives, ranged across Europe and Southwest Asia before their extinction approximately 30,000 years ago. Green et al. (p. [710][1]) report a draft sequence of the Neandertal genome, created from three individuals, and compare it with genomes of five modern humans. The results suggest that ancient genomes of human relatives can be recovered with acceptably low contamination from modern human DNA. Because ancient DNA can be contaminated with microbial DNA, Burbano et al. (p. [723][2]) developed a target sequence capture approach to obtain 14 kilobases of Neandertal DNA from a fairly poorly preserved sample with a high microbial load. A number of genomic regions and genes were revealed as candidates for positive selection early in modern human history. The genomic data suggest that Neandertals mixed with modern human ancestors some 120,000 years ago, leaving traces of Neandertal DNA in contemporary humans. [1]: /lookup/doi/10.1126/science.1188021 [2]: /lookup/doi/10.1126/science.1188046

279 citations

Journal ArticleDOI
Tyler Alioto1, Ivo Buchhalter2, Sophia Derdak1, Barbara Hutter2, Matthew D. Eldridge3, Eivind Hovig4, Lawrence E. Heisler5, Timothy Beck5, Jared T. Simpson5, Laurie Tonon, Anne Sophie Sertier, Ann-Marie Patch6, Ann-Marie Patch7, Natalie Jäger8, Natalie Jäger2, Philip Ginsbach2, Ruben M. Drews2, Nagarajan Paramasivam2, Rolf Kabbe2, Sasithorn Chotewutmontri2, Nicolle Diessl2, Christopher Previti2, Sabine Schmidt2, Benedikt Brors2, Lars Feuerbach2, Michael Heinold2, Susanne Gröbner9, Andrey Korshunov9, Patrick S. Tarpey10, Adam Butler10, Jonathan Hinton10, David T. Jones10, Andrew Menzies10, Keiran Raine10, Rebecca Shepherd10, Lucy Stebbings10, Jon W. Teague10, Paolo Ribeca1, Francesc Castro Giner1, Sergi Beltran1, Emanuele Raineri1, Marc Dabad1, Simon Heath1, Marta Gut1, Robert E. Denroche5, Nicholas J. Harding5, Takafumi N. Yamaguchi5, Akihiro Fujimoto, Hidewaki Nakagawa, Víctor Quesada11, Rafael Valdés-Mas11, Sigve Nakken4, Daniel Vodak4, Lawrence Bower3, Andy G. Lynch3, Charlotte Anderson3, Charlotte Anderson12, Nicola Waddell6, Nicola Waddell7, John V. Pearson6, John V. Pearson7, Sean M. Grimmond6, Sean M. Grimmond13, Myron Peto14, Paul T. Spellman14, Minghui He15, Cyriac Kandoth16, Semin Lee17, John Zhang17, John Zhang18, Louis Letourneau19, Singer Ma20, Sahil Seth18, David Torrents21, Liu Xi22, David A. Wheeler22, Carlos López-Otín11, Elias Campo23, Peter J. Campbell10, Paul C. Boutros24, Xose S. Puente11, Daniela S. Gerhard, Stefan M. Pfister2, Stefan M. Pfister9, John Douglas Mcpherson5, John Douglas Mcpherson24, Thomas J. Hudson5, Thomas J. Hudson24, Matthias Schlesner2, Peter Lichter2, Roland Eils9, Roland Eils2, David T. W. Jones2, Ivo Gut1 
TL;DR: It is shown that using PCR-free methods and increasing sequencing depth to ∼100 × shows benefits, as long as the tumour:control coverage ratio remains balanced, and many issues are in fact easy to remedy and have an immediate positive impact on mutation detection accuracy.
Abstract: As whole-genome sequencing for cancer genome analysis becomes a clinical tool, a full understanding of the variables affecting sequencing analysis output is required. Here using tumour-normal sample pairs from two different types of cancer, chronic lymphocytic leukaemia and medulloblastoma, we conduct a benchmarking exercise within the context of the International Cancer Genome Consortium. We compare sequencing methods, analysis pipelines and validation methods. We show that using PCR-free methods and increasing sequencing depth to ∼ 100 × shows benefits, as long as the tumour:control coverage ratio remains balanced. We observe widely varying mutation call rates and low concordance among analysis pipelines, reflecting the artefact-prone nature of the raw data and lack of standards for dealing with the artefacts. However, we show that, using the benchmark mutation set we have created, many issues are in fact easy to remedy and have an immediate positive impact on mutation detection accuracy.

278 citations

Journal ArticleDOI
TL;DR: In this review, the development of recombinant DNA technology has provided new tools for approaching yields improvement by means of genetic manipulation of biosynthetic pathways as applied to bioactive secondary metabolites produced by actinomycetes.

278 citations

Journal ArticleDOI
TL;DR: This review seeks to highlight the advantages of this technique in microbial fermentations monitoring and control, as well as in the development of more accurate kinetic models directed to bioprocesses optimization.

277 citations


Authors

Showing all 13643 results

NameH-indexPapersCitations
Russel J. Reiter1691646121010
Carlo Rovelli1461502103550
J. González-Nuevo144500108318
German Martinez1411476107887
Roland Horisberger1391471100458
Francisco Herrera139100182976
Javier Cuevas1381689103604
Teresa Rodrigo1381831103601
L. Toffolatti13637695529
Elias Campo13576185160
Gabor Istvan Veres135134996104
Francisco Matorras134142894627
Joe Incandela134154993750
Nikhil C. Munshi13490667349
Luca Scodellaro134174198331
Network Information
Related Institutions (5)
Complutense University of Madrid
90.2K papers, 2.1M citations

96% related

University of Valencia
65.6K papers, 1.7M citations

95% related

University of Barcelona
108.5K papers, 3.7M citations

95% related

Autonomous University of Barcelona
80.5K papers, 2.3M citations

94% related

Autonomous University of Madrid
52.8K papers, 1.6M citations

94% related

Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202396
2022268
20211,825
20201,913
20191,806
20181,721