Literature DB >> 26484064

Report from the 2nd Summer School in Computational Biology organized by the Queen's University of Belfast.

Frank Emmert-Streib1, Shu-Dong Zhang2, Peter Hamilton2.   

Abstract

In this paper, we present a meeting report for the 2nd Summer School in Computational Biology organized by the Queen's University of Belfast. We describe the organization of the summer school, its underlying concept and student feedback we received after the completion of the summer school.

Entities:  

Keywords:  Computational biology; Genomics data; High-throughput data

Year:  2014        PMID: 26484064      PMCID: PMC4535836          DOI: 10.1016/j.gdata.2013.12.001

Source DB:  PubMed          Journal:  Genom Data        ISSN: 2213-5960


Introduction

This year the 2nd Summer School in Computational Biology organized by the Queen's University of Belfast took place 16–18 September 2013 in Belfast (UK). The event gathered a total of 25 students from 5 different countries, making it so far the largest summer school since its establishment in 2012. The purpose of the summer school was to provide the participating students with a systematic introduction to quantitative analysis methods for high-throughput data that are needed to analyze genomics data from biological or biomedical experiments [1], [2]. Due to the fast paced progress of the field genomics, many university curricula have difficulties in catching-up with these developments, leaving room for a summer school like ours to provide the needed understanding for basic analysis principles and methods to the students to equip a new generation of scientists with the necessary skill set. In order to emphasize our goal for the summer school clearly we chose the subtitle: ‘Statistical and computational methods to analyze high-dimensional data in biology’. The summer school consisted of 18 lectures that were provided by 10 instructors, covering topics from introductory lectures for the statistical programming language R, microarray and next-generation sequencing (NGS) data to advanced analysis methods, including clustering, classification and survival analysis. In this paper, we provide a report about this summer school, including a discussion of student feedback we received after the completion of the summer school.

Meeting report

The underlying goal of our summer school was to teach students the necessary skill set for computational biology so these can be applied to, e.g., biological, biomedical or clinical data; see Fig. 1. Due to the interdisciplinary character of computational biology, which consists of a mixture of skills and knowledge from statistics, machine learning, computer science, biology and medicine, this is usually a long-lasting and challenging endeavor, because no student can have a background in all subjects. For this reason, we provided an introduction to all three basic subjects (see Fig. 1). In Fig. 2 we show the schedule of the summer school, comprising 18 lectures distributed over 3 days. We emphasize the main purpose of each lecture by the same color code as used in Fig. 1. The lecture notes for all lectures can be downloaded from http://www.bio-complexity.com/QUBsscb13/QUBsscb.html.
Fig. 1

A schematic overview of the constituting subjects of computational biology and its application domains. This visualization represents also the conceptual organization of the summer school.

Fig. 2

Schedule of the summer school. The colors correspond to the subjects in Fig. 1, indicating the emphasis of the corresponding lectures.

The covered topics range from a basic introduction to the statistical programming language R [3] (lectures 2, 4 & 5) to advanced statistical analysis methods, including classification, clustering, pathway analysis, survival analysis and connectivity mapping (lectures 9, 10, 11, 15, 16 & 17) [4], [5], [6], [7], [8], [9]. For each lecture, we aimed for a clear and hands-on explanation of a topic. For this reason we sacrificed a more comprehensive coverage, which would have forced us to extend the duration of the summer school considerably. The actual need for such a wide range of topics and difficulty levels becomes clear from the educational background of the students. In Fig. 3A, we show an overview of the subjects studied by the participating students of the summer school. As one can see, the majority of the students have an educational background in biology and biochemistry, however, there are also 29.5% of the students studying quantitive subjects (computer science, mathematics, statistics or physics). Furthermore, about half of the students are at the beginning of their university education (BSc student or MSc student) whereas the other half is on an advanced stage (PhD student or Postdocs), see Fig. 3B. This education diversity makes it challenging to provide an optimal level of the summer school lectures that fits all students equally. For this reason, we decided to provide basic lectures to give the students with a biology background the chance to catch-up basic skills that every student of a quantitative subject already has, and also to provide basic biology knowledge (lecture 3), e.g., computer science students to counterbalance their deficits.
Fig. 3

Overview statistics of the participating students in the summer school. A and B provide information about the educational background of the students. C–F show feedback from the students to the questions: Please describe the difficulty level of the summer school for you (C). Have you gained a basic understanding of the programming language R? (D). Have you gained a basic understanding of the statistical analysis of data? (3E). Have you gained a basic understanding of high-throughput technologies? (F).

In order to obtain feedback from the students regarding their experience from the summer school, we asked the students to fill in a questionnaire via ‘survey monkey’ after the completion of the summer school. In Fig. 3C we show the results for the question ‘Please describe the difficulty level of the summer school for you’. It is reassuring to see that the majority of students (70.6%) felt comfortable with the difficulty level of the provided lectures and none (0%) considered the summer school as ‘very difficult’. The next three questions we asked the students addressed their gained understanding from the summer school on different levels: Have you gained a basic understanding of the programming language R? See Fig. 3D. Have you gained a basic understanding of the statistical analysis of data? See Fig. 3E. Have you gained a basic understanding of high-throughput technologies? See Fig. 3F. Overall, the majority of the students are of the opinion that they gained a basic understanding in these 3 categories. Given the educational diversity of the students, see Fig. 3A and B, it is probably hard to improve these numbers substantially without increasing the duration of the summer school that would allow one to cover more basic and advanced grounds in considerably more depth. We would like to emphasize that the above discussion is not intended as a strict data analysis, but as a quantitative discussion of the feedback we received from the students.

Reproducible research

Aside from the actual topic of the summer school, teaching students the basics of computational biology, we intended to generate an awareness of the students for reproducible research [10], [11], [12]. In this respect, the key role of the statistical programming language R was discussed as a natural and efficient mediator between data, analysis methods and the conservation of the whole analysis process in a way that allows an error-free exchange/communication of a conducted analysis. Given the fact that it is anticipated to see in the next years an even increasing amount of data from more than one high-throughput technology, the reproducibility of a genomic data analysis, and means to realize it, is certainly becoming even more important in the near future.

Invited talk

Another feature of the summer school was to give the students the opportunity to see the application of the taught methods to real problems. For this reason, we invited Benjamin Haibe-Kains, from the Institut de Recherches Cliniques de Montreal (Canada), to provide a talk at the summer school. This talk was given at the end of the second day (see Fig. 2). Benjamin Haibe-Kains gave an interesting and exciting talk with the title Significance Analysis of Prognostic Signatures, which was based on recent results of his research [13], [14]. This allowed the students to experience the translation of analysis methods into clinical practice and to engage into a lively discussion, which helped them to realize the importance of computational biology. In this role to provide a lecture for the student, Benjamin Haibe-Kains is the successor of Simon Tavare, from the Statistics and Computational Biology Laboratory, Cancer Research UK Cambridge Research Institute, who provided last year's talk for our first summer school.

Conclusions

Overall, the experience we made during the last two years from organizing the Summer School in Computational Biology is very positive. We see not only a clear benefit for the students but also for ourselves, allowing us to provide more efficient lectures that can reach students with a heterogeneous educational background and professional level. For this reason the preparations for next year's summer school have already started and we anticipate the 3rd Summer School in Computational Biology to take place in September 2014.
  10 in total

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2.  Reproducible research in computational science.

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3.  Embracing the concept of reproducible research.

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4.  Reproducible research: a bioinformatics case study.

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6.  Angiogenic mRNA and microRNA gene expression signature predicts a novel subtype of serous ovarian cancer.

Authors:  Stefan Bentink; Benjamin Haibe-Kains; Thomas Risch; Jian-Bing Fan; Michelle S Hirsch; Kristina Holton; Renee Rubio; Craig April; Jing Chen; Eliza Wickham-Garcia; Joyce Liu; Aedin Culhane; Ronny Drapkin; John Quackenbush; Ursula A Matulonis
Journal:  PLoS One       Date:  2012-02-13       Impact factor: 3.240

7.  Connectivity Mapping for Candidate Therapeutics Identification Using Next Generation Sequencing RNA-Seq Data.

Authors:  Darragh G McArt; Philip D Dunne; Jaine K Blayney; Manuel Salto-Tellez; Sandra Van Schaeybroeck; Peter W Hamilton; Shu-Dong Zhang
Journal:  PLoS One       Date:  2013-06-26       Impact factor: 3.240

8.  Ensuring the statistical soundness of competitive gene set approaches: gene filtering and genome-scale coverage are essential.

Authors:  Shailesh Tripathi; Galina V Glazko; Frank Emmert-Streib
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Review 9.  Harnessing the complexity of gene expression data from cancer: from single gene to structural pathway methods.

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10.  Further steps toward functional systems biology of cancer.

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