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EMBL Australia – Group Leader in Biological Imaging

Posted by , on 13 October 2018

Closing Date: 15 March 2021

Group Leader in Biological Imaging (based at Monash University, Melbourne , Australia)

Expressions of interest are invited from scientists pushing technological boundaries in biological imaging, who seek to make major discoveries running their own independent research program. This EMBL Australia Group Leader position is hosted within the Biomedicine Discovery Institute at Monash University, Australia.

The successful applicant will be housed within the Department of Anatomy and Developmental Biology, one of the five Monash BDI departments.  Areas of research focus include renal, lung and reproductive biology, inflammation and cell death, epigenetics, embryology, cancer, stem cells, and cellular reprogramming.

Candidates with a background in developing and/or applying cutting edge imaging technology to address major biological questions are invited to apply. The University particularly welcomes applicants with significant experience and interest in lightsheet microscopy, super-resolution microscopy, and correlative light and electron microscopy.

For more details please visit the EMBL Australia website (http://www.emblaustralia.org/jobs) or the Monash University jobs pages (http://careers.pageuppeople.com/513/cw/en/job/582239/expression-of-interest-group-leader-embl-australia)

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This month in preLights – September

Posted by , on 12 October 2018

Welcome to our monthly summary of developmental biology (and related) preLights.

 

It’s been almost eight months since the launch of preLights, and we are very excited about the hugely positive response from the community so far and preLights’ rapid growth – we recently reached two hundred preprint highlights! To further grow this service, we will be announcing a call for recruiting new team members next month, so watch this space if you would like to join us as a preLighter.

The preLights posts from September turned out to be very diverse: from worms and insects to plants and fish, and also plenty of exciting novel techniques. We hope you enjoy this selection!

 

From Development to Disease

The early C. elegans embryo is a powerful model to tackle questions like how polarity initially emerges in a developing organism. Giuliana Clemente covered two studies that revealed a new role for Aurora A in symmetry breaking and polarity establishment in the worm.

Sarah Bowling discussed why cells die when they are not in the “right place” and highlighted a preprint showing that disrupted EGFR signaling, rather than a fitness recognition event through cell competition, is responsible. The preprint authors gave further insight into the study (check out the author’s response section) and pointed out that the simplest explanation to their question proved to be the correct one.

Erik Clark’s preLight showcased a conserved role for a posttranslational module (involving the micropeptide millepattes) in segmentation across many insect species, but a lack of segmentation phenotypes in Drosophila mutants. While they may not be good models for insect segmentation, Drosophila has provided numerous mechanistic insights into cell and tissue dynamics through the study of its developing egg chamber. Sundar Naganathan highlighted a preprint showing that in this model, 3D tissue elongation occurs through a mechanochemical signaling pathway that translates the external stiffness gradient into altered cadherin trafficking. Amanda Haage’s preLight also featured some fine mechanobiology in cancer cells, showing that actomyosin contractility regulates the activity of PKA, which is important for mechanically guided cell migration (durotaxis).

 

Figure taken from preprint by Ray et al.; highlighted by Erik Clark

 

From the plant development field, Martin Balcerowicz wrote about a study showing that two new proteins (Sol1 and Sol2) regulate fate transitions and cell divisions during Arabidopsis stomatal development.

Moving to zebrafish, Alberto Rosello-Diez featured a novel mechanism that initiates regeneration upon injury: in response to ROS signaling, Hegdehog-expressing cells are repositioned to create a new signaling center. Andreas van Impel reviewed zebrafish vasculature development and how the 50:50 balance of intersegmental arteries and veins is regulated by a flow-dependent mechanism. Excessive blood vessel formation, on the other hand, is a hallmark of cancer; Coert Margadant highlighted a promising strategy to inhibit blood vessel formation by blocking recycling of phosphoinositide lipids.

 

Several preprints harnessed the power of single-cell transcriptomics to gain insight into neural development and neurodegenerative disease. Zheng-Shan Chong covered a study exploring microglial development through scRNA-seq, which discovered a subset of postnatal neural cells resembling degenerative disease-associated microglia (DAM). Yen-Chung Chen preLighted two preprints looking at why not all neuron types are equally vulnerable in neurodegenerative diseases. Applying new transcriptomic techniques, LCM-seq and Axon-seq, potential protective mechanisms utilized by resistant somatic neurons were found. Finally, Carmen Adriaens’ preLight also dealt with high-throughput sequencing (promoter capture Hi-C), and explained the links between SNP-s associated with type 2 diabetes and chromatin architecture of human pancreatic islet cells.

 

Tools & Technologies

It’s difficult to imagine where the developmental biology field would be today without in situ hybridization techniques that detect mRNA localization. This month, Yen-Chung Chen highlighted work that developed a new fluorescent in situ hybridization method termed SABER, which is more sensitive, cheaper and quicker compared to previous FISH methods. To look at fluctuations in mRNA levels and whether these persist over multiple cell divisions, the preprint covered by Leighton Daigh combined Luria and Delbrück’s fluctuation analysis with population based mRNA sequencing (this new method was termed MemorySeq).

 

Figures taken from preprint by Kishi et al.; preLighted by Yen-Chung Chen

 

The number of preprints dealing with CRISPR technology is rapidly growing, but there is still a lot to be understood regarding the targeting and editing accuracy and efficacy in this system. Here, Rob Hynds preLighted a study that uncovered some general principles of CRISPR gene editing by analyzing a large set of indel profiles.

Jacky Goetz wrote about a new method that is able to quantify mechanical stress in vivo by injecting polyacrylamide beads into living embryos and analyzing their deformations. Finally, one of the favorites from this month was Samantha Seah’s preLight that discussed a new way of visualizing data using raincloud plots.

 

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Post-doctoral position in pancreatic tissue engineering available in the Spagnoli lab.

Posted by , on 12 October 2018

Closing Date: 15 March 2021

A Postdoctoral position is available in the Spagnoli lab. in the Centre for Stem Cell and Regenerative Medicine at King’s College, London. Our team uses interdisciplinary approaches to study pancreas development and stem cells. The candidate will be part of an exciting EU-funded FET-Open consortium aiming at bioengineering pancreatic tissue.

Developing therapies for pancreatic diseases, such as diabetes and pancreatic cancer, is hampered by a limited access to pancreatic tissue in vivo. Engineering three-dimensional (3D) tissue models, which accurately mimic the native organ, have great potential in biomedical applications, providing powerful platforms for studying tissue development and homeostasis and for modeling diseases. We have established a multi-disciplinary FET European consortium with the ambitious goal of developing an innovative bio-printing approach for generating pancreatic tissue. Tissues and organs comprise multiple cell types with specific biological functions that must be recapitulated in the printed tissue. We will biomimic developmental processes to fabricate 3D bio-printed pancreatic tissue units that allow sustained cell viability, expansion and functional differentiation ex vivo.

The Spagnoli lab. is coordinating the Consortium and will be primarily responsible for establishing a 3D-imaging and transcriptome atlas of pancreatic cells and defining cellular sources for engineering pancreatic tissue units. The candidate will be part of a young dynamic team and help in developing this ambitious research program. Moreover, the lab. is based at the Centre for Stem Cells & Regenerative Medicine (CSCRM) at King’s College London, which acts as the nucleus for a vibrant and collaborative stem cell research community, being an ideal environment for a successful postdoc experience.

Qualifications:

Applicants should have a recent Ph.D. degree or M.D./Ph.D. degree. Candidates with experience in stem cell and developmental biology, confocal microscopy, image acquisition and analysis will be preferred. This position seeks a highly motivated individual with a strong interest in developmental biology.

Starting date:

The position is open starting from October 2018 but later entry dates are possible. The initial contract is for one year and can be renewed until a maximum of three years.

Requirements:

A CV and a statement of research interests along with names of 2 referees should be sent via e-mail to the address below.

Contact:

Dr. Francesca M. Spagnoli, Centre for Stem Cell and Regenerative Medicine, KCL, London, UK

https://www.kcl.ac.uk/lsm/research/divisions/gmm/departments/stemcells/people/dr-francesca-spagnoli.aspx

francesca.spagnoli@kcl.ac.uk

Keywords:

Pancreas, Imaging, 3D cell engineering, ex vivo disease model, ex vivo organogenesis

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Singapore Fish Meeting 2018

Posted by , on 11 October 2018

On 2nd October 2018, the Mechanobiology Institute in Singapore hosted a meeting of Singapore-based researchers using fish in their work. We wanted to bring together the local community to build support and promote future research collaborations within Singapore. This meeting follows successful international conferences last year in Singapore, where the importance of fish in both fundamental and translational research was apparent (https://thenode.biologists.com/developmental-biologists-meet-lion-city/events/, https://www.zdmsociety.org/past-events).

The fish community in Singapore, despite running up against the usual funding challenges and regulations, remains a formidable group. Over 80 people attended during the afternoon, with the room literally full to bursting, Figure 1. Researchers came from National University of Singapore, Nanyang Technological University (both universities recently built state-of-the-art fish facilities), A*Star and Duke-NUS (Figure 2).

Figure 1.  Top: Timothy Saunders addressing an overwhelming crowd of scientists in the Singapore Fish Meeting 2018. Bottom: Anticipation of the first talk.

The half-day meeting saw presentations by twelve young scientists (students, post-docs and research associates). There was also a poster session going on late into the evening, including one on a wide-screen LED TV (Figure 3). Notably, women presenters made up more than half (9/12 talks and 6/11 posters) of the presenters, deriving from a roughly equal proportion of male and female participants. The talks comprised a wide-ranging topics from fundamental biology, through to medical applications and engineering. A clear strength was in the use of fish in disease modelling, but there were also interesting presentations related to ageing, behaviour, and fluid mechanics.  It was a powerful demonstration of the versatility of fish models for studying a broad range of topics. It was particularly stimulating to get fresh research ideas and tools, and also to immerse ourselves in the work of our colleagues covering unfamiliar territory.

Figure 2.  Affiliation breakdown of participants in the Singapore Fish Meeting 2018. NUS – National University of Singapore (including the Cancer Science Institute and Mechanobiology Institute); IMB – Institute of Medical Biology; IMCB – Institute of Molecular and Cell Biology; NTU – Nanyang Technological University; TLL – Temasek Life Sciences Laboratory.

 

The day finished with pizza and wine, which provided a platform for cross-fertilization of expertise to spawn new ideas and projects. The fish meeting was a wonderful success – great talks, lively discussions, and good food.  It was also an important opportunity to bring together the local fish community. We believe that the fish community in Singapore will continue to do great science and be a driving force of scientific discoveries through inter-disciplinary cooperation.

Figure 3.  Abraha (hidden) presenting his Next-Gen poster to a group of curious scientists.

The community would also like to take this opportunity to remember the late Professor Hong Yunhan from National University of Singapore, who pioneered the generation of haploid medaka stem cells.

About the Authors:

Dr. Jason Lai has just graduated from the Stainier Lab in Bad Nauheim, Germany to pursue his post-doctoral training with Timothy Saunders. He is interested in growth and form, particularly related to the Hippo/YAP pathway (https://www.researchgate.net/profile/Jason_Lai6)

Asst. Prof. Timothy Saunders is a principal investigator at the Mechanobiology Institute, Singapore (https://mbi.nus.edu.sg/timothy-saunders/saunders-lab/). He brings his background in physics to tackle problems in developmental biology, such as how complex organ form emerges. He has recently published his first work in Zebrafish, collaborating with Prof. Philip Ingham (https://www.cell.com/developmental-cell/fulltext/S1534-5807(18)30697-X).

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PhD position Denholm lab

Posted by , on 10 October 2018

Closing Date: 15 March 2021

Emergence of functional polarity in a tubular epithelium

Epithelial tubes often have a functional polarity written along their proximo-distal (P-D) axis, with different segments of specialised cell-types carrying out distinct physiological activities. With a handful of notable exceptions, we know very little about how P-D axes and segment-specific differentiation are regulated during organogenesis.

The major objective of this project is to understand the molecular and cellular mechanisms that pattern and maintain functional polarity along the P-D axis in a structurally simple, but functionally sophisticated epithelial tube: the insect renal tubule.

The project will be carried out in the laboratory of Barry Denholm (Biomedical Sciences, University of Edinburgh)

About the lab and department:

https://www.ed.ac.uk/discovery-brain-sciences/our-staff/research-groups/barry-denholm

https://denholmlab.wordpress.com

https://twitter.com/denholmlab

Further information about the project and details of how to apply:

https://www.findaphd.com/search/ProjectDetails.aspx?PJID=100840

https://www.ed.ac.uk/roslin/postgraduate/studentships/emergence-of-functional-polarity-in-a-tubular-epithelium

Completed application form along with your curriculum vitae should be sent to our PGR student team at RDSVS.PGR.Admin@ed.ac.uk

Download application and reference forms via: https://www.ed.ac.uk/roslin/postgraduate/bbsrc-eastbio-dtp

Closing Date:  5thDecember 2018

 

Poster:

PhD Position Denholm lab

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PhD in Developmental Systems Biology – The Origins of Retinal Self-Organisation

Posted by , on 9 October 2018

Closing Date: 15 March 2021

A fully-funded 4-year BBSRC PhD project on
The Origins of Retinal Self-Organisation

 

Application Deadline: 26th November 2018

 

Location: School of Biological Sciences, University of East Anglia, Norwich, UK

 

Project Description:

There is much interest in the possibility of growing human organs from patient stem cells in vitro (a.k.a. ‘organoids’). In addition to regenerative therapies, this could furnish new disease models and facilitate drug development. By learning how tissues and organs self-organise in the embryo, we can rationally design strategies to improve and expand organoid technologies. Our research uses the chick embryo to investigate the development of our primary sense organ, the eye.

It is known that stem cell cultures can spontaneously self-organise to form retinas in vitro, but it is not know how they do this. This PhD project aims to investigate a Pax6 gene network that may drive self-organisation of the early retina. Pax6 was named a ‘master control gene’ for eye development, and we recently identified a network of Pax6-interacting genes with the potential to spontaneously self-organise the early retina, either in the embryo or in vitro. The project will directly test this possibility by measuring the biophysical properties of key gene products and comparing them with values predicted by computer simulations of early retinal development.

Through this project you will develop transferable ‘wet lab’ skills in molecular, cell, and developmental biology, and advanced imaging. You will receive rigorous training in quantitative analytical approaches, with an added opportunity to gain new skills in computational biology (computer programming, mathematical modelling).

 

For informal enquiries and further information, please contact: Dr Tim Grocott (t.grocott@uea.ac.uk)

 

To check eligibility and apply, please visit: https://t.co/KZcWVCLZYB

 

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The 29th Mammalian Genetics and Development Workshop

Posted by , on 9 October 2018

A meeting of the Genetics Society on 29th November 2018 at the UCL Institute of Child Health, London.

Organisers: Nick Greene (UCL), Cynthia Andoniadou (KCL), Andy Copp (UCL)

Abstract submission deadline: 5pm, 8th November

 

The Mammalian Genetics and Development Workshop is an annual meeting focusing on the development and genetics of mammals.  The Meeting is based on the submitted abstracts, and include diverse topics ranging from mammalian development (not exclusively human or mouse) and identification of disease genes and developmental mechanisms, to human genetics and epigenetics. Other model systems (including Drosophila, zebrafish and chick) are also welcomed where these relate to general developmental questions and/or disease models.

The meeting will be similar format to the 28th Meeting in 2017, which had a fantastic set of short talks covering various aspects of developmental biology, mouse models of human disorders and genetics of human disease (abstracts are published at https://doi.org/10.1017/S0016672317000076)

The workshop is traditionally a venue for post-docs and PhD students to talk rather than laboratory heads and is an excellent training ground and a friendly, informal forum. In keeping with this objective, we offer TWO PRIZES of £150 to individual post-graduate/post-doctoral presenters. In addition, thanks to the generosity of Mammalian Genome (https://link.springer.com/journal/335) publishers, we will offer an additional PRIZE of £150.

 

Registration: A £10 registration fee is payable by all attendees on arrival at the meeting.  This fee covers the abstract booklet, tea and coffee refreshments and the wine reception.  Speakers and chairpersons will be provided with lunch, free of charge, on the day of their presentation.

 

Abstract Submission: All Workshop presentations will be in lecture format (15 or 20 minutes).  Please send your abstract by e-mail (Word or rtf file) to ich.mgdwshop@ucl.ac.uk by 5pm on 8th November. In addition please indicate the length of talk you prefer.

 

Abstract format is as follows: Title (bold), AUTHORS (ALL CAPS), Address (italics) and text (200 word limit). Abstracts will be published (with the authors’ permission) in Genetics Research (https://www.cambridge.org/core/journals/genetics-research).

 

 

https://www.ucl.ac.uk/child-health/research/developmental-biology-and-cancer-programme/developmental-biology-and-cancer-meetings/mgdw-0

 

 

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Biology and Disease Mechanisms of Drosophila Axonal Endoplasmic Reticulum

Posted by , on 9 October 2018

Closing Date: 15 March 2021

We have a vacancy for a postdoctoral research associate, funded by a BBSRC grant, to work on the roles of spastic paraplegia gene products in formation of axonal ER, and identification of new genes and cellular processes involved in this. For some background on the project, see: https://elifesciences.org/articles/23882.

Applicants should have a PhD in a biological science, interests in neuronal cell biology, and experience in as many as possible of the following: model organism genetics, genetic screens, neuronal cell biology, light or electron microscopy, live imaging, molecular biology, and bioinformatics.

Informal enquiries to Dr. Cahir O’Kane, c.okane@gen.cam.ac.uk, Twitter @OKaneCahir, http://www.gen.cam.ac.uk/research-groups/okane

Closing date 30th October; funding for 3 years in the first instance. For more details, and to apply, see: http://www.jobs.cam.ac.uk/job/19044/

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The developing brain in health and disease: Scientific Meeting

Posted by , on 8 October 2018

The Academy of Medical Sciences is convening a scientific meeting on the 19 and 20 March 2019, in Oxford. Abstract submission deadline: 5 November 2018.

This meeting will explore key areas of neurodevelopmental research in a unique forum that emphasises discussion and collaboration between disciplines, career stages and sectors.

One of the key aims will be to highlight the latest advances in neurodevelopmental research and identify key research questions that could bring a real impact to the field. The meeting’s talks and discussions will span a broad range of neurodevelopmental and disorder research, from in utero to adolescence, and from multiple perspectives, including molecular, cellular, circuit/systems and behavioural levels.

We welcome researchers from all backgrounds to attend this meeting and strongly encourage early career researchers, from PhD level onwards, to apply. Registration is free.

Please find more information in the Academy’s website: https://acmedsci.ac.uk/developingbrainmeeting

The meeting poster, with the list of speakers, can be downloaded here: The_Developing_Brain_Poster_Digital

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Make a difference: the alternative for p-values

Posted by , on 8 October 2018

Calculation and reporting of p-values is common in scientific publications and presentations (Cristea and Ioannidis, 2018). Usually, the p-value is calculated to decide whether two conditions, e.g. control and treatment, are different. Although a p-value can flag differences, it cannot quantify the difference itself (footnote 1). Therefore, p-values fail to answer a very relevant question: “How large is the difference between the conditions?” (Gardner and Altman, 1986; Cumming, 2014). The aforementioned question can be answered by calculating the “effect size”, which quantifies differences. Calculation and interpretation of effect sizes is straightforward and therefore a good alternative for calculating p-values (Ho, 2018). In the figure below, I transformed an ordinary plot with p-values into graphs that depict (i) the data and (ii) the difference between median values as the effect size. The calculation and application of effect sizes is the topic of this blog.

Figure 1: Transformation of an ordinary graph with p-values into a visualization of the data and the difference between median values as the effect size. Values indicate the difference between the median and the median of the ‘wt’ Condition. The horizontal lines and the values between brackets indicate the 95% confidence interval.

 

Why do we need an alternative for p-values?

The null-hypothesis significance test (NHST) compares the central tendency of two samples, e.g. the mean for parametric or median for nonparametric tests. Next to the central tendency (or location), it takes into account the precision of that value. Since the precision increases with increasing sample size, the outcome of a NHST depends on sample size (Nakagawa and Cuthill, 2007) as also explained here. In other words, the p-value reflects both the difference in central tendency and the number of observations. This is just one of the issues with p-values, other issues that should be considered when using p-values are discussed elsewhere (Goodman, 2008). Due to the issues with p-values, it has been recommended to replace (Cumming, 2014; Halsey et al., 2015) or supplement (Wasserstein and Lazar, 2016) p-values with alternative statistics. Effect sizes, aka estimation statistics, are a good alternative (Claridge-Chang and Assam, 2016).

 

Effect size

In statistics, the effect size reflects the difference between conditions. In contrast with p-values the effect size is independent of sample size. Effect sizes are expressed as relative (footnote 2) or absolute values. Here, I will only discuss the absolute effect size. The absolute effect size is the difference between central tendency of samples. Commonly used measures of central tendency are the mean and median for normal and skewed distributions respectively. Hence, for a normal distribution the effect size is the difference between the two means.

 

Quantification of differences

To illustrate the calculation and use of effect sizes, I will use data from an experiment in which the area of individual cells was measured under three conditions (Figure 1). There is an untreated (wt) condition and two treated samples. The question is how the treatment affects the cell area. When the distribution of the observed areas is non-normal (as is the case here), the median better reflects the central tendency (i.e. typical value) of the sample. Therefore, it is more adequate for this experiment to calculate the difference between the medians (Wilcox, 2010). The median values for TIAM, wt and LARG are 1705 µm², 1509 µm² and 1271 µm² respectively. From these numbers, it follows that the effect of TIAM is an increase of area by 1705 µm² – 1509 µm² = 196 µm². The effect of LARG is a decrease in cell area of 1271 µm² – 1509 µm² = -238 µm². Note that the difference is expressed in the same units (e.g. µm²) as the original measurement and is therefore easy to understand. 

 

Confidence intervals

As mentioned before, the difference will not depend on sample size. On the other hand, the precision will depend on sample size. More observation per experimental condition will generate median values with a lower error. As a consequence, the difference will be more precisely defined with a larger sample size (Drummond and Tom, 2011). To indicate the precision of the difference, the 95% confidence interval (95CI) is a suitable measure (Cumming, 2014). For differences between means, the 95CI can be calculated directly (see here or here for calculation with R) but for the difference between medians it is not straightforward.

 

 

Figure 2: Step-by-step explanation of the calculation and visualization of the effect size and 95% confidence intervals. Step 1) bootstrapping of the data results in a collection of 1000 new median values. Step 2) the difference between the conditions (LARG and TIAM) and the control (wt) is calculated by subtraction, yielding 1000 differences (or effect sizes). Step 3) the middle value (median) of the distribution defines the effect size and the borders encompassing 95% of the differences define the 95% confidence interval (95CI, values between brackets). Medians are indicated with a circle and the 95CI with a horizontal line.

 

Median difference with confidence intervals

In a previous blog, I explained how bootstrapping can be used derive the 95CI of the median. Briefly, bootstrapping is resampling of existing data in silico, typically 1000 times. This process simulates repeating the actual experiment (footnote 3). Bootstrapping can be done with the data of the experiment, for each of the conditions, yielding 1000 median values which are displayed in figure 2 (step 1). The 1000 medians reflect a distribution of values that would have been obtained, if the experiment were to be repeated 1000x. These bootstrapped medians can be used to calculate the effect size, i.e. difference between the median of the control group and the other conditions. The result of the calculation is 1000 difference values per condition (figure 2, step 2). The resulting distribution of the differences can be used to determine the 95CI. As explained previously, the 95CI is taken from the middle 95% of the data, i.e. the values at the 2.5th and 97.5th percentile (figure 2, step 3). Thus, by bootstrapping we obtain the difference between medians and the 95CI (footnote 4).

 

Result and interpretation

The resulting graph shows two effect sizes with confidence intervals. All values are in the original units (µm²) and therefore these numbers make sense. The effect of TIAM is an area change of 207 µm² with a 95CI that ranges from 27 µm² to 439 µm² (footnote 5). The confidence interval can be listed between brackets: [27,439]. Since the 95CI does not overlap with zero (as also clear from the graph in figure 1 and 2), this is interpreted as a significant change (at an alpha level of 0.05). On the other hand, the effect of LARG is -206 [-350,35] µm². Since the 95CI does overlap with zero for this condition, this implies that there is no conclusive evidence for an effect. Note that the interpretation of the confidence intervals is consistent with the p-values listed in figure 1. For more information on the interpretation of effect size and 95CI see table 5.2 by Yatano (2016).

 

Conclusion

The effect size is the difference between conditions. It is of great value for the quantitative comparison of data and it is sample size independent. Another advantage is that the effect size is easy to understand (in contrast to p-values, which are often misunderstood or misinterpreted). The benefit of the bootstrap procedure to derive the confidence intervals is that it delivers a distribution of differences. The distribution conveys a message of variability and uncertainty, reducing binary thinking. So, make a difference by adding the effect size to your graph. The effect size facilitates interpretation and can supplement or replace p-values.

 

Acknowledgments: Thanks to Franka van der Linden and Eike Mahlandt for their comments.

 

Availability of data and code

The data and R-script to prepare the figures is available at Zenodo: https://doi.org/10.5281/zenodo.1421371

A web-based application (using R/ggplot2) for calculating and displaying effect sizes and 95CI (based on bootstrapping) is currently under development: https://github.com/JoachimGoedhart/PlotsOfDifferences

A preview of the web app is available here.

 

Footnotes

Footnote 1: The actual definition of a p-value is: The probability of the data (or more extreme values) given that (all) the assumptions of the null hypothesis are true.

Footnote 2: Examples of relative effect size are Cohen’s d and Cliff’s delta. The Cliff’s delta is distribution independent (i.e. robust to outliers) and can be calculated using an excel macro, see: Goedhart (2016)

Footnote 3: Bootstrapping assumes that the sample accurately reflects the original population that was sampled. In other words, it assumes that the sampling was random and that the samples are independent. These assumptions also apply to other inferential statistics, i.e. significance tests.

Footnote 4: The website www.estimationstats.com (developed by Adam Claridge-Chang and Joses Ho) uses bootstrapping to calculate the effect size and 95CI for the difference of means. It is also a good source for information on effect sizes.

Footnote 5: Bootstrapping depends on random resampling, and therefore the numbers will be slightly different each time that resampling is performed.

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