Cameron Neylon

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Cameron Neylon
Cameron Neylon in 2013 at the CERN Workshop on Innovations in Scholarly Communication (OAI8).jpg
Cameron Neylon in 2013
Born
David Cameron Neylon
Alma mater
Known for
Awards Blue Obelisk award (2010)
Scientific career
Fields
Institutions
Thesis Towards the directed molecular evolution of DNA-binding specificity  (1999)
Website

David Cameron Neylon is an advocate for open access and Professor of Research Communications at the Centre for Culture and Technology at Curtin University. [3] [4] From 2012 - 2015 they were the Advocacy Director at the Public Library of Science. [1] [5] [6] [7] [8]

Contents

Education

Neylon was educated at the University of Western Australia [ citation needed ] and the Australian National University where they were awarded a Doctor of Philosophy degree in Biophysics in 1999 for work on directed molecular evolution and DNA-binding specificity. [9] [10]

Career

In 2009 Neylon was a senior scientist at the ISIS neutron source of the Science and Technology Facilities Council. [11] From 2012 to 2015 they served as director of advocacy at the Public Library of Science. [12] They joined The Centre for Culture and Technology (CCAT) at Curtin University in 2015 as Professor of Research Communications. [3] [4]

Neylon is an original drafter of the Panton Principles and opposed the Research Works Act [13] and advocates for governmental encouragement for researchers to use open access licensing. [14] [15]

Neylon advocates for the use of altmetrics in determining the impact of scholarly publications. [16] [17]

Awards and honours

In 2010 they accepted a Blue Obelisk award. [18]

Related Research Articles

Computational biology involves the development and application of data-analytical and theoretical methods, mathematical modelling and computational simulation techniques to the study of biological, ecological, behavioural, and social systems. The field is broadly defined and includes foundations in biology, applied mathematics, statistics, biochemistry, chemistry, biophysics, molecular biology, genetics, genomics, computer science, and evolution.

PLOS Nonprofit open-access publisher

PLOS is a nonprofit open-access science, technology, and medicine publisher with a library of open-access journals and other scientific literature under an open-content license. It launched its first journal, PLOS Biology, in October 2003 and publishes seven journals. The organization is based in San Francisco, California, and has a European editorial office in Cambridge, Great Britain. The publications are primarily funded by payments from the authors.

Euarchontoglires superorder of mice, humans, their most recent common ancestor, and all descendants

Euarchontoglires is a clade and a superorder of mammals, the living members of which belong to one of the five following groups: rodents, lagomorphs, treeshrews, colugos and primates.

Origin of replication Sequence in a genome

The origin of replication is a particular sequence in a genome at which replication is initiated. Propagation of the genetic material between generations requires timely and accurate duplication of DNA by semiconservative replication prior to cell division to ensure each daughter cell receives the full complement of chromosomes. This can either involve the replication of DNA in living organisms such as prokaryotes and eukaryotes, or that of DNA or RNA in viruses, such as double-stranded RNA viruses. Synthesis of daughter strands starts at discrete sites, termed replication origins, and proceeds in a bidirectional manner until all genomic DNA is replicated. Despite the fundamental nature of these events, organisms have evolved surprisingly divergent strategies that control replication onset. Although the specific replication origin organization structure and recognition varies from species to species, some common characteristics are shared.

SOS response Biological process

The SOS response is a global response to DNA damage in which the cell cycle is arrested and DNA repair and mutagenesis is induced. The system involves the RecA protein. The RecA protein, stimulated by single-stranded DNA, is involved in the inactivation of the repressor (LexA) of SOS response genes thereby inducing the response. It is an error-prone repair system that contributes significantly to DNA changes observed in a wide range of species.

Michael Ashburner

Michael Ashburner is a biologist and Emeritus Professor in the Department of Genetics at University of Cambridge. He is also the former joint-head and co-founder of the European Bioinformatics Institute (EBI) of the European Molecular Biology Laboratory (EMBL) and a Fellow of Churchill College, Cambridge.

Poly (ADP-ribose) polymerase

Poly (ADP-ribose) polymerase (PARP) is a family of proteins involved in a number of cellular processes such as DNA repair, genomic stability, and programmed cell death.

<i>PLOS Medicine</i> Academic journal

PLOS Medicine is a peer-reviewed weekly medical journal covering the full spectrum of the medical sciences. It began operation on October 19, 2004, as the second journal of the Public Library of Science (PLOS), a non-profit open access publisher. All content in PLOS Medicine is published under the Creative Commons "by-attribution" license. To fund the journal, the publication's business model requires in most cases that authors pay publication fees. The journal was published online and in a printed format until 2005 and is now only published online. The journal's acting chief editor is Clare Stone, who replaced the previous chief editor, Larry Peiperl, in 2018.

Cohesin A protein complex that regulates the separation of sister chromatids during cell division

Cohesin is a protein complex that mediates sister chromatid cohesion, homologous recombination and DNA looping. Cohesin is formed of SMC3, SMC1, SCC1 and SCC3. Cohesin holds sister chromatids together after DNA replication until anaphase when removal of cohesin leads to separation of sister chromatids. The complex forms a ring-like structure and it is believed that sister chromatids are held together by entrapment inside the cohesin ring. Cohesin is a member of the SMC family of protein complexes which includes Condensin, MukBEF and SMC-ScpAB.

Steven Salzberg

Steven Lloyd Salzberg is an American computational biologist and computer scientist who is a Bloomberg Distinguished Professor of Biomedical Engineering, Computer Science, and Biostatistics at Johns Hopkins University. He is a member of the Institute of Genetic Medicine at Johns Hopkins School of Medicine, where he is also Director of the Center for Computational Biology.

<i>PLOS One</i> Peer-reviewed open access scientific journal

PLOS One is a peer-reviewed open access scientific journal published by the Public Library of Science (PLOS) since 2006. The journal covers primary research from any discipline within science and medicine. The Public Library of Science began in 2000 with an online petition initiative by Nobel Prize winner Harold Varmus, formerly director of the National Institutes of Health and at that time director of Memorial Sloan–Kettering Cancer Center; Patrick O. Brown, a biochemist at Stanford University; and Michael Eisen, a computational biologist at the University of California, Berkeley, and the Lawrence Berkeley National Laboratory.

The recombination-activating genes (RAGs) encode parts of a protein complex that plays important roles in the rearrangement and recombination of the genes encoding immunoglobulin and T cell receptor molecules. There are two recombination-activating genes RAG1 and RAG2, whose cellular expression is restricted to lymphocytes during their developmental stages. The enzymes encoded by these genes, RAG-1 and RAG-2, are essential to the generation of mature B cells and T cells, two types of lymphocyte that are crucial components of the adaptive immune system.

Transcription activator-like effector nuclease

Transcription activator-like effector nucleases (TALEN) are restriction enzymes that can be engineered to cut specific sequences of DNA. They are made by fusing a TAL effector DNA-binding domain to a DNA cleavage domain. Transcription activator-like effectors (TALEs) can be engineered to bind to practically any desired DNA sequence, so when combined with a nuclease, DNA can be cut at specific locations. The restriction enzymes can be introduced into cells, for use in gene editing or for genome editing in situ, a technique known as genome editing with engineered nucleases. Alongside zinc finger nucleases and CRISPR/Cas9, TALEN is a prominent tool in the field of genome editing.

PRDM9

PR domain zinc finger protein 9 is a protein that in humans is encoded by the PRDM9 gene. PRDM9 is responsible for positioning recombination hotspots during meiosis by binding a DNA sequence motif encoded in its zinc finger domain. PRDM9 is the only speciation gene found so far in mammals, and is one of the fastest evolving genes in the genome.

An ultra-conserved element (UCE) is a region of DNA that is identical in at least two different species. One of the first studies of UCEs showed that certain human DNA sequences of length 200 nucleotides or greater were entirely conserved in human, rats, and mice. Despite often being noncoding DNA, some ultra-conserved elements have been found to be transcriptionally active, giving non-coding RNA molecules.

Panton Principles

The Panton Principles are a set of principles which were written to promote open science. They were first drafted in July 2009 at the Panton Arms pub in Cambridge.

Article-level metrics are citation metrics which measure the usage and impact of individual scholarly articles.

Environmental DNA DNA that is collected from a variety of environmental samples such as soil, seawater, snow or even air rather than directly sampled from an individual organism

Environmental DNA or eDNA is DNA that is collected from a variety of environmental samples such as soil, seawater, snow or even air rather than directly sampled from an individual organism. As various organisms interact with the environment, DNA is expelled and accumulates in their surroundings from various sources. Example sources of eDNA include, but are not limited to, feces, mucus, gametes, shed skin, carcasses and hair. Such samples can be analyzed by high-throughput DNA sequencing methods, known as metagenomics, metabarcoding, and single-species detection, for rapid monitoring and measurement of biodiversity. In order to better differentiate between organisms within a sample, DNA metabarcoding is used in which the sample is analyzed and uses previously studied DNA libraries, such as BLAST, to determine what organisms are present.

Kaustuv Sanyal

Kaustuv Sanyal is an Indian molecular biologist, mycologist and a professor at the Molecular Biology and Genetics Unit of the Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR). He is known for his molecular and genetic studies of pathogenic yeasts such as Candida and Cryptococcus). An alumnus of Bidhan Chandra Krishi Viswavidyalaya and Madurai Kamaraj University from where he earned a BSc in agriculture and MSc in biotechnology respectively, Sanyal did his doctoral studies at Bose Institute to secure a PhD in Yeast genetics. He moved to the University of California, Santa Barbara, USA to work in the laboratory of John Carbon on the discovery of centromeres in Candida albicans. He joined JNCASR in 2005. He is a member of the Faculty of 1000 in the disciplines of Microbial Evolution and Genomics and has delivered invited speeches which include the Gordon Research Conference, EMBO conferences on comparative genomics and kinetochores. The Department of Biotechnology of the Government of India awarded him the National Bioscience Award for Career Development, one of the highest Indian science awards, for his contributions to biosciences, in 2012. He has also been awarded with the prestigious Tata Innovation Fellowship in 2017. The National Academy of Sciences, India elected him as a fellow in 2014. He is also an elected fellow of Indian Academy of Sciences (2017), and the Indian National Science Academy (2018). In 2019, he has been elected to Fellowship in the American Academy of Microbiology (AAM), the honorific leadership group within the American Society for Microbiology.

References

  1. 1 2 Segaran, Toby; Hammerbacher, Jeff, eds. (2009). Beautiful Data: The Stories Behind Elegant Data Solutions. O'Reilly. ISBN   978-0596157111.
  2. Cameron Neylon publications indexed by Google Scholar
  3. 1 2 Lab, CCAT (25 August 2015). "CCAT Welcomes Professor Cameron Neylon". curtin.edu.au. Archived from the original on 4 March 2016. Retrieved 25 August 2015.
  4. 1 2 View staff profile
  5. Neylon, C. (2012). "More Than Just Access: Delivering on a Network-Enabled Literature". PLOS Biology. 10 (10): e1001417. doi:10.1371/journal.pbio.1001417. PMC   3479106 . PMID   23109911.
  6. Neylon, Cameron (28 March 2013). "Cameron Neylon calls for greater precision in the use of open-access terminology". Times Higher Education . Retrieved 26 June 2013.
  7. Neylon, Cameron (7 September 2011). "Cameron Neylon: Time for total scientific openness". New Scientist (2828). doi:10.1016/S0262-4079(11)62148-9 . Retrieved 26 June 2013.
  8. Neylon, C. (2013). "Architecting the Future of Research Communication: Building the Models and Analytics for an Open Access Future". PLOS Biology. 11 (10): e1001691. doi:10.1371/journal.pbio.1001691. PMC   3805469 . PMID   24167448.
  9. Neylon, David Cameron (1999). Towards the directed molecular evolution of DNA-binding specificity (PhD thesis). Australian National University.
  10. Neylon; Brown, S. E.; Kralicek, A. V.; Miles, C. S.; Love, C. A.; Dixon, N. E. (2000). "Interaction of the Escherichia coli replication terminator protein (Tus) with DNA: a model derived from DNA-binding studies of mutant proteins by surface plasmon resonance" (PDF). Biochemistry. 39 (39): 11989–11999. doi:10.1021/bi001174w. PMID   11009613.
  11. Coturnix (28 December 2009). "ScienceOnline09 – an interview with Cameron Neylon – A Blog Around The Clock". ScienceBlogs . Retrieved 26 June 2013.
  12. Yaplee, Darlene (27 March 2012). "Cameron Neylon to Join PLoS as Director of Advocacy | PLOS". plos.org. Archived from the original on 24 June 2013. Retrieved 26 June 2013.
  13. Crotty, David (25 April 2012). "An Interview with Cameron Neylon, PLoS' New Director of Advocacy". Scholarly Kitchen . Retrieved 26 June 2013.
  14. Neylon, C. (2012). "Science publishing: Open access must enable open use". Nature. 492 (7429): 348–349. Bibcode:2012Natur.492..348N. doi:10.1038/492348a. PMID   23257864. S2CID   21225124.
  15. Konkel, Frank (27 Feb 2013). "White House research directive responds to We the People petition, builds on NIH policies -- FCW". Federal Computer Week . Retrieved 26 June 2013.
  16. Neylon, C.; Wu, S. (2009). "Article-Level Metrics and the Evolution of Scientific Impact". PLOS Biology. 7 (11): e1000242. doi:10.1371/journal.pbio.1000242. PMC   2768794 . PMID   19918558.
  17. Nielsen, Michael (10 August 2010). "Cameron Neylon on practical steps toward open science". michaelnielsen.org. Retrieved 26 June 2013.
  18. "SourceForge.net: Blue Obelisk Awards - blueobelisk". sourceforge.net. 2012. Archived from the original on 2012-11-14. Retrieved 26 June 2013.