Sonika Tyagi
Monash University, Clayton campus
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Briefings in Bioinformatics | 2013
Nathan S. Watson-Haigh; Catherine A. Shang; Matthias Haimel; Myrto Kostadima; Remco Loos; Nandan Deshpande; Konsta Duesing; Xi Li; Annette McGrath; Sean McWilliam; Simon Michnowicz; P. Moolhuijzen; Steve Quenette; Jerico Revote; Sonika Tyagi; Maria Victoria Schneider
The widespread adoption of high-throughput next-generation sequencing (NGS) technology among the Australian life science research community is highlighting an urgent need to up-skill biologists in tools required for handling and analysing their NGS data. There is currently a shortage of cutting-edge bioinformatics training courses in Australia as a consequence of a scarcity of skilled trainers with time and funding to develop and deliver training courses. To address this, a consortium of Australian research organizations, including Bioplatforms Australia, the Commonwealth Scientific and Industrial Research Organisation and the Australian Bioinformatics Network, have been collaborating with EMBL-EBI training team. A group of Australian bioinformaticians attended the train-the-trainer workshop to improve training skills in developing and delivering bioinformatics workshop curriculum. A 2-day NGS workshop was jointly developed to provide hands-on knowledge and understanding of typical NGS data analysis workflows. The road show–style workshop was successfully delivered at five geographically distant venues in Australia using the newly established Australian NeCTAR Research Cloud. We highlight the challenges we had to overcome at different stages from design to delivery, including the establishment of an Australian bioinformatics training network and the computing infrastructure and resource development. A virtual machine image, workshop materials and scripts for configuring a machine with workshop contents have all been made available under a Creative Commons Attribution 3.0 Unported License. This means participants continue to have convenient access to an environment they had become familiar and bioinformatics trainers are able to access and reuse these resources.
F1000Research | 2017
Rafael C. Jimenez; Mateusz Kuzak; Monther Alhamdoosh; Michelle Barker; Bérénice Batut; Mikael Borg; Salvador Capella-Gutierrez; Neil Chue Hong; Martin Cook; Manuel Corpas; Madison Flannery; Leyla Garcia; Josep Ll. Gelpí; Simon Gladman; Carole A. Goble; Montserrat González Ferreiro; Alejandra Gonzalez-Beltran; Philippa C. Griffin; Björn Grüning; Jonas Hagberg; Petr Holub; Rob W. W. Hooft; Jon Ison; Daniel S. Katz; Brane Leskošek; Federico López Gómez; Luis J. Oliveira; David Mellor; Rowland Mosbergen; Nicola Mulder
Scientific research relies on computer software, yet software is not always developed following practices that ensure its quality and sustainability. This manuscript does not aim to propose new software development best practices, but rather to provide simple recommendations that encourage the adoption of existing best practices. Software development best practices promote better quality software, and better quality software improves the reproducibility and reusability of research. These recommendations are designed around Open Source values, and provide practical suggestions that contribute to making research software and its source code more discoverable, reusable and transparent. This manuscript is aimed at developers, but also at organisations, projects, journals and funders that can increase the quality and sustainability of research software by encouraging the adoption of these recommendations.
F1000Research | 2017
Philippa C. Griffin; Jyoti Khadake; Kate LeMay; Suzanna E. Lewis; Sandra Orchard; Andrew J. Pask; Bernard J. Pope; Ute Roessner; Keith Russell; Torsten Seemann; Andrew E. Treloar; Sonika Tyagi; Jeffrey H. Christiansen; Saravanan Dayalan; Simon Gladman; Sandra B. Hangartner; Helen L. Hayden; William Ho; Gabriel Keeble-Gagnere; Pasi K. Korhonen; Peter Neish; Priscilla R. Prestes; Mark F. Richardson; Nathan S. Watson-Haigh; Kelly L. Wyres; Neil D. Young; Maria Victoria Schneider
Throughout history, the life sciences have been revolutionised by technological advances; in our era this is manifested by advances in instrumentation for data generation, and consequently researchers now routinely handle large amounts of heterogeneous data in digital formats. The simultaneous transitions towards biology as a data science and towards a ‘life cycle’ view of research data pose new challenges. Researchers face a bewildering landscape of data management requirements, recommendations and regulations, without necessarily being able to access data management training or possessing a clear understanding of practical approaches that can assist in data management in their particular research domain. Here we provide an overview of best practice data life cycle approaches for researchers in the life sciences/bioinformatics space with a particular focus on ‘omics’ datasets and computer-based data processing and analysis. We discuss the different stages of the data life cycle and provide practical suggestions for useful tools and resources to improve data management practices.
Briefings in Bioinformatics | 2016
Nathan S. Watson-Haigh; Jerico Revote; Radoslaw Suchecki; Sonika Tyagi; Susan M. Corley; Catherine A. Shang; Annette McGrath
Abstract There is a clear demand for hands-on bioinformatics training. The development of bioinformatics workshop content is both time-consuming and expensive. Therefore, enabling trainers to develop bioinformatics workshops in a way that facilitates reuse is becoming increasingly important. The most widespread practice for sharing workshop content is through making PDF, PowerPoint and Word documents available online. While this effort is to be commended, such content is usually not so easy to reuse or repurpose and does not capture all the information required for a third party to rerun a workshop. We present an open, collaborative framework for developing and maintaining, reusable and shareable hands-on training workshop content.
Molecular metabolism | 2018
Aneta Stefanidis; Nicole M. Wiedmann; Sonika Tyagi; Andrew M. Allen; Matthew J. Watt; Brian J. Oldfield
Objective The potential for brown adipose tissue (BAT) to be targeted as a therapeutic option to combat obesity has been heightened by the discovery of a brown–like form of inducible “beige” adipose tissue in white fat which has overlapping structural and functional properties to “classical” BAT. The likelihood that both beige and brown fat are recruited functionally by neural mechanisms, taken together with the lack of a detailed understanding of the nature of changes in the nervous system when white adipose tissue (WAT) is transformed to brown, provides the impetus for this study. Here, we aim to identify whether there is a shift in the gene expression profile in neurons directly innervating inguinal white adipose tissue (iWAT) that has undergone “beiging” to a signature that is more similar to neurons projecting to BAT. Methods Two groups of rats, one housed at thermoneutrality (27 °C) and the other exposed to cold (8 °C) for 7 days, were killed, and their T13/L1 ganglia, stellate ganglion (T1/T2), or superior cervical ganglion (SCG, C2/3) removed. This approach yielded ganglia containing neurons that innervate either beiged white fat (8 °C for 7 days), inguinal WAT (27 °C for 7 days), BAT (both 27 °C and 8 °C for 7 days) or non-WAT (8 °C for 7 days), the latter included to isolate changes in gene expression that were more aligned with a response to cold exposure than the transformation of white to beige adipocytes. Bioinformatics analyses of RNA sequencing data was performed followed by Ingenuity Pathway Analysis (IPA) to determine differential gene expression and recruitment of biosynthetic pathways. Results When iWAT is “beiged” there is a significant shift in the gene expression profile of neurons in sympathetic ganglia (T13/L1) innervating this depot toward a gene neurochemical signature that is similar to the stellate ganglion projecting to BAT. Bioinformatics analyses of “beiging” related genes revealed upregulation of genes encoding neuropeptides proopiomelanocortin (POMC) and calcitonin-gene related peptide (CGRP) within ganglionic neurons. Treatment of differentiated 3T3L1 adipocytes with αMSH, one of the products cleaved from POMC, results in an elevation in lipolysis and the beiging of these cells as indicated by changes in gene expression markers of browning (Ucp1 and Ppargc1a). Conclusion These data indicate that, coincident with beiging, there is a shift toward a “brown-like” neurochemical signature of postganglionic neurons projecting to inguinal white fat, an increased expression of POMC, and, consistent with a causative role for this prohormone in beiging, an αMSH-mediated increase in beige gene markers in isolated adipocytes.
Briefings in Bioinformatics | 2017
Maria Victoria Schneider; Phillippa C. Griffin; Sonika Tyagi; Madison Flannery; Saravanan Dayalan; Simon Gladman; Nathan S. Watson-Haigh; Philipp E. Bayer; Michael Charleston; Ira R. Cooke; Rob Cook; Richard J. Edwards; David Edwards; Dominique Gorse; Malcolm J. McConville; David R. Powell; Marc R. Wilkins; Andrew Lonie
Abstract EMBL Australia Bioinformatics Resource (EMBL-ABR) is a developing national research infrastructure, providing bioinformatics resources and support to life science and biomedical researchers in Australia. EMBL-ABR comprises 10 geographically distributed national nodes with one coordinating hub, with current funding provided through Bioplatforms Australia and the University of Melbourne for its initial 2-year development phase. The EMBL-ABR mission is to: (1) increase Australia’s capacity in bioinformatics and data sciences; (2) contribute to the development of training in bioinformatics skills; (3) showcase Australian data sets at an international level and (4) enable engagement in international programs. The activities of EMBL-ABR are focussed in six key areas, aligning with comparable international initiatives such as ELIXIR, CyVerse and NIH Commons. These key areas—Tools, Data, Standards, Platforms, Compute and Training—are described in this article.
Journal of the American College of Cardiology | 2018
James K. Fahey; Sarah Williams; Sonika Tyagi; David R. Powell; Jeannette C. Hallab; Gulrez Chahal; Mirana Ramialison; Anthony J. White
Spontaneous coronary artery dissection (SCAD) is a clinical event, affecting female patients almost exclusively, in which intramural hematoma develops in a coronary artery and manifests as acute coronary syndrome [(1)][1]. The pathogenesis is unknown, although it is distinct from that of
Human Reproduction | 2018
Te-Sha Tsai; Sonika Tyagi; Justin C. St. John
F1000Research | 2017
Sarah Williams; Sonika Tyagi; David R. Powell
F1000Research | 2017
Sonika Tyagi; Maria Victoria Schneider; Sarah L. Morgan; Michael Charleston; Patricia M. Palagi; Judit Kumuthini; Gabriella Rustici; Teresa K. Attwood