- Meeting report
- Open Access
The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlights
BMC Genomics volume 17, Article number: 747 (2016)
The Third International Genomic Medicine Conference (3rd IGMC) was organised by the Centre of Excellence in Genomic Medicine Research (CEGMR) at the King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia (KSA). This conference is a continuation of a series of meetings, which began with the first International Genomic Medicine Conference (1st IGMC, 2011) followed by the second International Genomic Medicine Conference (2nd IGMC, 2013). The 3rd IGMC meeting presented as a timely opportunity to bring scientists from across the world to gather, discuss, and exchange recent advances in the field of genomics and genetics in general as well as practical information on using these new technologies in different basic and clinical applications. The meeting undoubtedly inspired young male and female Saudi researchers, who attended the conference in large numbers, as evidenced by the oversubscribed oral and poster presentations. The conference also witnessed the launch of the first content for npj Genomic Medicine, a high quality new journal was established in partnership by CEGMR with Springer Nature and published as part of the Nature Partner Journal series. Here, we present a brief summary report of the 2-day meeting including highlights from the oral presentations, poster presentations, workshops, poster prize-winners and comments from the distinguished scientists.
Given the resounding success of the Second International Genomic Medicine Conference (2nd IGMC) and the publication of its outcome , the Center of Excellence in Genomic Medicine Research (CEGMR) continued its trend of open science discussion and organized the Third International Genomic Medicine Conference (3rd IGMC, 30th November to 1st December 2015) (http://igmc-cegmr.org/Default.aspx) at the King Faisal Convention Hall, King Abdulaziz University (KAU). The 3rd IGMC provided a focused and in depth view of the latest research findings relating to cancer, genetics, genomic medicine, reproductive medicine, ageing, metagenomics and metabolomics, personalized genomics, biobanking, bioinformatics, along with many other interesting topics. At least 500 leading international researchers, renowned national scientists including those from KAU dedicated scientific faculty, participated proactively presenting their latest research findings. All the recognized universities and research organizations in Saudi Arabia including CEGMR, Center of Innovation in Personalized Medicine (CIPM), King Fahd Medical Research Center (KFMRC) and King Abdulaziz City for Science and Technology (KACST) participated. The following countries were represented: Canada, Egypt, Germany, Japan, Qatar, Spain, Switzerland, Tunisia, Turkey, United Kingdom (UK), and United States of America (USA).
One of the major events of the meeting was the announcement and launch of the first issue of the npj Genomic Medicine, a journal that was established by CEGMR in partnership with the Nature Publishing Group (NPG). In addition, a significant number of private companies attended the conference and took advantage of the meeting to present their state-of-the-art products, and services supporting genome research. Workshops (for all participants and others for local training endeavors) were organized over 3 days following the 2-day symposium. Here, we report the overall events and activities of the meeting including oral presentations, poster sessions, workshops, poster prize winners and comments from highly distinguished guest speakers about the meeting.
3rd IGMC 1st day, opening and welcoming session
On 30th of November, the conference began symbolically with an opening ceremony and welcome reception proceeding with the recitation of Holy Quran. The session was chaired by Professor Adeel Chaudhary, Deputy Director at CEGMR and Vice Dean of the Faculty of Applied Medical Sciences, KAU. On the stage, the Chief Guest, His Highness Vice President Professor Adnan Zahid and the Director of CEGMR, Professor Mohammed Al-Qahtani were seated to accord the occasion. A large number of foreign delegates, guests of honor, scientists, faculty and participants from a variety of institutes were in attendance. Professor Mohammed Al-Qahtani, gave a welcome address (Table 1) and recalled the interdepartmental, regional and international collaborations that have been fostered since the inception of the center and how notable progress has been achieved and sustained as a result of these collaborations. As a mark of respect to the University, Professor Al-Qahtani presented a memento to Professor Adnan Zahid who obliged by accepting it. Professor Al-Qahtani presented Dr. Abdulaziz Al-Swailem, Vice President, King Abdulaziz City for Science and Technology (KACST), Riyadh, KSA who then delivered an important speech in which he briefed the attendees on the launch of the second phase of the next 5 year KACST research plan (Maarifah Two) (Table 1). In addition, further funding opportunities were presented by Dr. Omar El-Farouk, the Director of Qatar National Research Fund (QNRF), Qatar Foundation, Doha, Qatar. The attendees found this talk, in particular, a golden opportunity to apply for funding outside Saudi Arabia, which would be an excellent vehicle for networking amongst researchers working in Gulf countries.
The 3rd IGMC meeting, for the first time, invited a senior member (Dr. Nazeeh Al-Othmany) from the Saudi Food and Drug Administration (SFDA) who presented a detailed view of the workings of the organization, its aims and how all members of the SFDA organization are continuously trying to help and facilitate the mission of scientists at the research centers within Saudi Arabia. The welcoming session ended with a presentation by Dr. Magdalena Skipper, the npj Executive Editor, NPG, UK who presented the model of the partnership between the NPG and CEGMR, which has led to establishment of the first npj journal in the Middle East, npj Genomic Medicine (http://0-www.nature.com.brum.beds.ac.uk/npjgenmed/). This fruitful partnership between NPG and KAU has led to establishment of a second npj journal, npj Climate and Atmospheric Science, http://0-www.nature.com.brum.beds.ac.uk/npjclimatsci/. Later, the Editor-in-Chief Dr. Stephen Scherer of npj Genomic Medicine announced the launch of the first issue of the journal. After Dr. Skipper’s talk the proceedings of the conference were declared open and all attendees settled to scientific business.
3rd IGMC 1st day, session I: genomics of cancer, aging and complex diseases
The second session on Day 1 was dedicated mainly to “Genomics of Cancer, Ageing and Complex Diseases” (Table 2). This session was chaired by the distinguished Professor Angel Carracedo, a prominent clinician scientist affiliated with KAU, Professor Adnan Merdad (School of Medicine, KAU) and Professor Abdelbaset Buhmeida (CEGMR, KAU). The first talk was the keynote lecture given by Professor Jerry W. Shay from the Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, USA on “Ageing and Cancer: Are Telomeres and Telomerase the Connection?” Professor Shay discussed the regulation over long distances of genes by telomere length. He elucidated his group’s discovery using 3D Co-FISH and a modified method of chromosome capture followed by high-throughput sequencing (Hi-C) to identify a significant number of genes within the first 10 Mb distal to the telomeres on many chromosomes regulated by telomere length. Professor Shay showed that the human telomerase reverse transcriptase (TERT) locus was also linked with looped chromatin structures in cells with long telomeres but was reduced in cells with shorter telomeres. He termed telomere length dependent regulation of gene expression as telomere position effects over long distances (TPE-OLD). He also showed that gene expression was regulated by telomere length long before telomeres become short enough to initiate a DNA damage response. These findings demonstrated a novel function for telomeres and also suggested a new mechanism for how progressive telomere shortening might affect human age associated disease initiation and progression.
The keynote lecture was followed by a presentation by Professor Stephen Scherer from the Centre for Applied Genomics, Hospital for Sick Children and University of Toronto, Canada on “Genomic basis for autism spectrum and related disorders”. He explained the substantial contribution of non-coding variants to the aetiology of autism spectrum disorders (ASD) and highlighted the significance of using whole genome sequencing (WGS) for comprehensive genetic analyses. A novel observation shared was an increased frequency of de novo mutations near to de novo copy number variations residing on the maternal chromosome. He also discussed how to integrate epigenomic data with whole genome sequence data and interpret complex data through clustering approaches. He further emphasized the importance of performing WGS of 10,000 individuals with ASD and their family members and applying this data to diagnostic and drug treatment design .
Professor Albert Fornace from the Lombardi Comprehensive Cancer Center, Georgetown University, USA then spoke on “Integration of metagenomics and metabolomics in gut microbiome research”. Professor Fornace presented his research group’s various discoveries using metagenomics and metabolomics strategies to understand the correlative nature of the microbe/host co-metabolism to distinguish the regulatory functions of microbiota in preserving the health of the host. He further explained the potential of host/microbial interaction studies to define causality, response to treatment, risk prediction, and keystone species to exploit as probiotics in diseases such as inflammatory bowel disease (IBD) or colonic inflammation (colitis) triggered by immune-radiotherapy.
Professor Nobutaka Hirokawa from the Departments of Cell Biology and Anatomy, and Molecular Structure and Dynamics, University of Tokyo, Japan presented interesting talk titled “KIF2A regulates postnatal axons and its deficiency causes malformation of cortical development and epilepsy”. He presented his findings on the importance of Kinesin-13 super family protein 2A (KIF2A), an ATP-dependent microtubule destabilizer, in the development of precise neuronal circuits, prenatal cell survival, migration and the elongation of axons. He further described various studies to decipher the role of KIF2A in neuronal development using tamoxifen-inducible conditional KIF2A knockout mice. He showed that the loss of KIF2A led to hippocampal sclerosis, dentate mossy fiber (MF) sprouting, and recurrent excitatory circuits resembling but different from temporal lobe (TLE) and these phenotypes developed without excitation. More importantly, he showed that the conditional KIF2A granule cells displayed failed axon/dendrite differentiation, and developed multiple short axons throughout the entire molecular layer.
Then Dr. Deema Hussain from KFMRC, KAU gave a presentation on “A unique integrated system to discern pathogenesis of central nervous system tumours”. Her presentation focused on the establishment of a unique integrated system to facilitate the analysis of multiple bio-parameters of distinct central nervous system tumours (CNST) such as meningiomas, astrocytomas, oligodendrogliomas, medulloblastomas and glioblastomas. She explained about generating cell lines from CNST for further genetic, biochemical, cytological and pharmacological analysis. She also elaborated further on the importance of gene expression profiling of uncultured tumour samples to enable identification of several novel prognostic markers for meningiomas, including the recently associated cancer stem cell marker called anterior gradient protein 2 homolog (AGR-2). Dr. Deema concluded that the integrated analysis approach was essential for the development of safe, efficacious and potent targeted therapeutic modalities for CNST.
The final presentation of the second session on Day 1 was delivered by Dr. Heba Alkhattabi from CEGMR on “RPL27A, a novel target for miR-595 and its contribution to myelopoiesis via ribosomal dysgenesis”. She discussed the identification of several targets for miR-595 including a large ribosomal subunit RPL27A using a novel method. Dr. Alkhattabi explained that the down regulation of RPL27A triggered p53 activation, apoptosis and inhibited proliferation. More significantly, she showed that p53-independent effects were observed secondarily to a reduction in the ribosome subunit 60s with associated ribosome dysgenesis. In addition, RPL27A overexpression did not influence the p53 mRNA levels but enhanced proliferation. RPL27A knockdown in normal CD34+ cells specially inhibited erythroid proliferation and differentiation. Dr. Alkhattabi concluded that haploinsufficiency of miR-595 in Myelodysplastic Syndromes (MDS) patients with - 7/del 7q may contribute to disease pathogenesis via RPL27A modulation since miR-595 was significantly down regulated in these patients with −7/-7q anomalies.
The final scientific session of the first day (Session III) was on "Genomics applications towards personalized medicine" (Table 3) with all presentations focused on the theme of how the latest advancements in genomics could translate to personalization, also referred to as the precision or personalized medicine. Professor Emmanouil Dermitzakis from the Department of Genetic Medicine and Development, University of Geneva Medical School, Switzerland highlighted the genotype-tissue expression (GTEx) project, where multiple 'non-diseased' tissue samples collected from recently deceased human donors could be used for analysis across tissues and individuals. The patterns of transcriptome variations across individuals and tissues and their association with human phenotypes can be analyzed using GTEx data. Furthermore, quantification of gene expression by RNA-sequencing on GTEx samples had high concordance with microarray based quantification, thus indicating the value of the samples. Recent advances in tumor biology will enable personalization of cancer therapeutics with reliance on information from the International Cancer Genome Consortium (ICGC), The Cancer Genome Atlas (TCGA) and the Cancer Genome Project (CGP) as well as the understanding of the oncogenic drivers, the genes involved in disease progression, the identification of biomarkers and the development of drugs for specific targets.
Along similar lines, Professor Anna Goodeve from Sheffield Diagnostic Genetic Service, Sheffield Children's NHS Foundation Trust, UK, shared her experience on how next generation sequencing (NGS) and gene panels have extended diagnostic capability in analyzing blood related disorders. The haemostasis and platelet gene panel which included 13 genes and another panel consisting of 16 genes that are currently known to be associated with Fanconi's anaemia (FA) were sequenced using the Illumina MiSeq or HiSeq. Dr. Goodeve’s results revealed that the haemostasis and platelet panel enabled identification of pathogenic candidate mutations in 62 % of the patients. The FA panel led to the identification of biallelic mutations (33 %), heterozygous mutations (13 %), homozygous mutations (13 %), other gene mutations (7 %) and no mutations (33 %). She concluded that the use of NGS provides a single laboratory workflow for analysis of gene panels for different disorders and considerably reduces time to achieve a definitive diagnosis.
In the final presentation of this session, Dr. Ashraf Dallol, from the CIPM/CEGMR at KAU, explained the usefulness of targeted sequencing of cancer mutational hotspots in combination with the Ion Torrent Personal Genome Platform in a cohort of colorectal cancer (CRC) cases from Saudi Arabia. CRC is a heterogeneous disease influenced by genetic and epigenetic variations acting as passengers or drivers of the tumor. Dr. Dallol showed that analysis of the mutational status of 2,800 catalogued somatic mutations in cancer (COSMIC) mutations of 50 oncogenes and tumor suppressor genes in CRC would enable understanding the genetic background for this cohort and thus pave the way to precision medicine (PM).
3rd IGMC 2nd day, session I, biobanking in the post-genomic era
Since the completion of the Human Genome Project in 2003, a significant increase in the number of Biobanks (also called Biorepositories including their improved design, scale and governance) has been observed worldwide. The main aim of establishing these banks was to support effective genomic research and personalized healthcare. Nowadays, Biobanks are considered as the main core around which OMICs research and advanced clinical applications are carried out to drive PM . However, a major PM challenge research community currently facing is the need for a large scale of high-quality and fully annotated bio- specimens. To address such challenge, thousands of biobanks in developed countries have been established and are currently working towards harmonizing their practices internationally . However, this big number of biobanks established in the developing countries needs to establish crucial resources to overcome lack of knowledge, awareness, and practice (KAP) in addition to other technical, operational, ethical and regulatory challenges.
Therefore, the 3rd IGMC “Biobanking in the Post-Genomic Era” session (Table 4) was aimed at raising the level of knowledge and awareness of the research community and public within Saudi Arabia, the Gulf region and at the international level in order to draw attention to the importance of this critical resource. During the session, the quantity and quality of biospecimens were highlighted by both international (Professor Jim Vaught) and national (Professor Abdelbaset Buhmeida) speakers. They demonstrated that this issue is fundamental in order to produce effective diagnostic tools and tailor customized drugs to enhance the clinical service offered to patients. The need for additional high quality and fully annotated biospecimens processed using Standard Operating Procedures (SOPs) was also highlighted as one of the top priorities of biomedical research in order to deliver more accurate downstream diagnostic test results. Dr. Ibrahim Alabdulkareem from the National Guard Health Affairs, Riyadh, KSA and Professor Jaudah Al-Maghrabi from Pathology Department, College of Medicine, KAU, Jeddah, KSA strongly emphasized this issue. The Biobank session witnessed extensive discussion from the audience and this was marked by motivation from both patients who attended this session to donate their biospecimens and scientists who requested support and guidelines from CEGMR biobanks.
IGMC 2nd day, session II: bioinformatics applications in genomic medicine
The continuous development of new OMICs technologies has led to generation of unprecedented large data sets. Handling and analysis of these OMICs data to extract meaningful and clinically actionable targets are serious challenges . Additional approaches are required to achieve integrative analysis of heterogeneous data. That is to tailor meaningful predictions and associations of the data in order to better understand the molecular pathology of diseases to improve targeted treatment [6, 7]. With the integration of OMICs in modern healthcare, the 3rd IGMC dedicated a session to “Bioinformatics applications in genomic medicine” (Table 5). Given the complexity of cancer, the session started with a presentation by Professor Sudhir Kumar, Department of Biology, Temple University, Philadelphia, USA, who showed an analysis of cancer heterogeneity assessed from an evolutionary prospect and demonstrated its use in tracing the origins, patterns, and evolutionary relationships of homologous sequences of cancer clones (clonotypes) to overcome the hurdle of cancer heterogeneity for diagnosis, prognosis and therapeutics .
Moving from the genome-wide association study (GWAS) scale to target specific rare and disease-specific variations was another major focus of the conference delivered by Professor Angel Carracedo from Legal Medicine Santiago de Compostela University, Spain. He showed that moving from GWAS-driven associations to causality is a key turning point towards personalized medicine. However, a further filtering step of the large number of associations revealed by GWAS with reduced heritability is necessary to identify causality or susceptibility targets. Professor Carracedo suggested new targeted re-sequencing of GWAS association targets in order to refine both the scale and mapping of the genomic hits. These identified hits would provide clues to decrypting the molecular pathways.
Professor Carracedo’s talk was followed by that of Professor Hossam Faheem from Fujitsu Technology Solutions International, Japan who showed that several factors including computer science, medical informatics, Biobanking LIMS (Laboratory Information Management System), bioinformatics, biostatistics and OMICs datasets should be joined to tailor a clinical integrative analysis workflow of heterogeneous datasets in order to drive the current transition from OMICs-based science to OMICs-based healthcare. He showed that advanced computational tools such as the supercomputing facilities with superior memory to accommodate parallel and computationally intensive applications’ needs offer excellent solution which are now implemented at KAU (named as AZIZ supercomputer facility).
The bioinformatics session ended with a presentation by Dr Sajjad Kareem from CEGMR who highlighted developing a new web application called E-GRASP which allows: (i) SNPs view including information about SNPid, PMID, P-value, chromosome, position, number of studies and phenotypes for each SNPs, (ii) studying view; which explains unique SNPs replication in each studies and phenotypes and (iii) evolutionary view which describes evolutionary information including E-value for SNP phenotype association, E-rank of the evolutionary rate and time span of the position retrieved from the “E-rank Web Server” for each SNP. Dr. Karim concluded that E-GRASP is a more representative database with additional information of SNPs replication and evolutionary scores, facilitating the comprehensive qualitative and quantitative analysis.
IGMC 2nd day, session III: reproductive medicine in the 21st century
The investigation of disease aetiologies requires a complex and multidimensional approach. Sufficient understanding of these diseases origins and susceptibility is an important prerequisite. Thus, investigation of germline genomic instability (mutations and epi-mutations) and its role in disease heritability and/or susceptibility during reproductive and embryonic phase will provide clues about diseases’ origin and relevant causative genomic variations. The Reproductive Medicine in the 21st Century Session at the 3rd IGMC was dedicated to highlight the revolution in reproductive and developmental medicine due to the OMICs-based application that can offer successful and cost-effective solutions.
Dr. Aisha Elaimi from the CEGMR/KAU (Table 6) highlighted how an experimental animal model system, such as the Embryoscope™, can be used to assess the developmental stages of an embryo directly from two cell to blastocyst stages in the presence or absence of pharmacological agents. Such an experimental system can be utilized to have a better understanding of the impact of blastulation rate and aneuploidy or DNA fragmentation, which in turn can lead to personalized therapeutic applications.
Dr. Serdar Coskun from King Faisal Specialist Hospital and Research Center, Riyadh, KSA addressed the issue of the OMICs scale applications and their impact in preimplantation genetic testing (PGT), where only one or a few cells are available for genomic analysis. He showed that the development of single cell whole genome amplification (scWGA) technologies enabled obtaining sufficient high-quality DNA from the initial minute starting material . Dr. Coskun showed that PGT allowed the birth of a healthy baby who can potentially donate either the cord blood or haematopoietic stem cells to treat another ill patient.
Professor Ashok Agarwal, Center for Reproductive Medicine, The Cleveland Clinic, Cleveland, USA, focused his presentation on addressing new research into the causes of male infertility including proteomics which is the new frontier of research in male infertility as it allows the identification of numerous sperm-specific proteins. Prof. Agarwal concluded that proteomics provides a greater understanding of protein functions involved in sperm processes such as motility, capacitation, acrosome reaction and fertilization.
The reproductive medicine session wrapped up with a presentation by Professor Eberhard Nieschlag, Center for Reproductive Medicine and Andrology, University Hospital of Muenster, Germany, who focused on the Klinefelter Syndrome (KS) and its relationship with infertility. He showed that the incidence of KS in the general male population is 1:500 and among 23,000 patients of the Center for Reproductive Medicine and Andrology at the University of Muenster, Germany is 1:52, whereas in Saudi Arabia the incidence is 1:11 in selected patients with azoospermia or sperm counts <5 mill/ml. Professor Nieschlag’s presentation drew the attention to the serious impacts of the KS on Saudi infertility patients.
The scientific sessions of the 3rd IGMC were accompanied by eight workshops. These workshops offered the opportunity for local researchers to enhance their practical knowledge as well as to introduce the novice to the wide array of applications and cutting edge technologies available to researchers. The practical IGMC workshops covered a range of areas such as molecular cytogenetics in medicine, molecular genetics, flow cytometry in oncology, bioinformatics, high throughput DNA sequencing and microarrays. One additional workshop was introduced for the first time in the IGMC, the publication workshop, which was very well-received by the participants. Overall, the high demand for such wide range of training was demonstrated by the large number of applicants (n = 48) enrolling in the workshops. The venue for training was provided by CEGMR at KAU and many of the workshops were overseen and delivered by highly distinguished, international faculty who participated in the IGMC conference in a number of capacities. The success of the workshops program demonstrated the desire and enthusiasm of many local researchers to extend their knowledge in different fields and further develop their professional capabilities.
3rd IGMC young scientists’ poster winners
The conference organizers recognized the importance of motivating young scientists and hence offered prizes for the best poster presentations. Nearly two hundred posters were displayed covering a wide range of research topics. A selected committee critically assessed the displays; posed questions to the participants; evaluate their explanations on the subject; and on the basis of a set of criteria, selected for the three top poster presentations. Each winner received a certificate and a monetary award. The first prize (5000 Saudi Riyals, SR) was awarded to Olfat Al-Harazi from the Department of Biostatistics, Epidemiology and Scientific Computing, King Faisal Specialist Hospital and Research Centre, Riyadh, KSA (Poster number 30) titled ‘’Breast Cancer Incidence and Genomic Signature in Young and Old Women in Saudi Arabia and Western Countries‘’. The second prize (4000 SR) went to Nezar Al-hebshi, Department of Preventive Dentistry, College of Dentistry, Jazan University, Jazan, KSA (Poster number 23) titled ‘’Mutational landscape of Arabian snuff-associated oral squamous cell carcinoma‘’. The third prize (SR 3000) was earned by Nada Salem from CEGMR/KAU, KSA (Poster number 105) titled: ‘’Integrated use of evolutionary information in GWAS reveals important SNPs in Asthma‘’.
3rd IGMC scientific committee members
This committee consisted of nine members whose role was to carefully review the abstracts, make final decisions on the acceptance or rejection of submitted abstracts, and to decide which abstracts would be presented either as a poster or as an oral presentation. The members of the scientific committee are as follows:
Dr. Muhammad Abu-Elmagd
Dr. Ashraf Dallol
Professor Jerry W. Shay
Dr. Gauthaman Kalamegam
Dr. Mourad Assidi
Professor Abdelbaset Buhmeida
Dr. Farid Ahmed
Professor Stephen W. Scherer
Professor Bruce Budowle
Dr. Hans H. Schulten
Editing the 3rd IGMC abstracts’ and articles’ supplements was led by Dr. Muhammad Abu-Elmagd who worked as the editor of both supplements. The 3rd IGMC abstracts’ supplement was published in BMC Genomics (https://0-bmcgenomics-biomedcentral-com.brum.beds.ac.uk/articles/supplements/volume-17-supplement-6). The articles' supplement containing 16 peer-reviewed articles was published in a number of BMC journals including BMC Genomics, BMC Medical Genetics, BMC Cancer and BMC Structural Biology. The final decision on accepting and rejecting manuscripts was made by the Executive Editor of BMC Genomics.
Thoughts about the 3rd IGMC by eminent scientists
Guest keynote speaker Professor Jerry W. Shay: ‘’This was by far the most successful International Genomic Medicine Conference that was held in Jeddah, November 2015. There was a very large number of attendees that led to many discussions about science enabling many new collaborations. The invited speakers were excellent, covering diverse areas of genomics and human disease. The organization of the meeting was simply outstanding. Everything worked from registration, the overall program and most importantly the poster sessions. As one of the judges of the poster sessions, I had many conversations with young scientists. Their excitement about their work was contagious and will certainly have a future positive impact for science in the Kingdom of Saudi Arabia‘’.
The Director of the Centre for Applied Genomics, The Hospital for Sick Children and The Director of McLaughlin Centre for Molecular Medicine, University of Toronto, Canada, Professor Stephen Scherer: ‘’The meeting was memorable because all of the discussions were grounded in science and in data quality including interpretation of results. The session on Biobanking was very important since this can be done 'right' or it can be done 'wrong' and there needs to be scholarly discussion early on in decision-making. Perhaps, most importantly, I was energized by the excitement of the younger people participating at the meeting including many who traveled from remote regions of the Kingdom. There were many good lessons to be learned from the locals, national, and international participants‘’.
The Director of the American Center for Reproductive Medicine, Cleveland Clinic, USA, Professor Ashok Agarwal: ‘’I am pleased to share my impressions of the Third International Genomics Medicine Conference organized by the Center for Excellence in Genomic Medicine Research at King Abdulaziz University, Jeddah, Saudi Arabia in November 2015. The meeting was nicely organized in a pleasant venue, it had a large number of attendees and a galaxy of highly recognized speakers from many parts of the world. The keynote lectures went really well; there was lively discussion after these talks. The presentation by local team of researchers was of high quality and a good indicator of future developments in the field of genomic medicine. I came back with good memories of the excellent scientific discourse, opportunity to meet and listen to both local and international scientists and most importantly the warm hospitality of the local organizing committee‘’.
The 3rd International Genomic Medicine Centre set a stage for the next round of planning and scientific investment in the area of individualized (precision) medicine in Saudi Arabia . The active participation of female Saudi scientists was unprecedented. The conference witnessed the launch of the first issue of npj Genomic Medicine, a journal CEGMR/KAU has established in partnership with the Nature Publishing Group (NPG) that promises to expand publishing options in the Middle East and around the world. The conference workshops offered extensive training to the participants in a wide range of genomics tools and approaches. The take away message from most talks was that studying the population structure and health challenges confronting Saudi Arabia and by openly publishing the results would not only help people in this region, but also provide lessons for other countries around the world.
- 3rd IGMC:
The Third International Genomic Medicine Conference
Assisted reproductive technologies
Autism spectrum disorders
Centre of excellence in genomic medicine research
Cancer genome project
Center of innovation in personalized medicine
Central nervous system tumours
Saudi Food and Drug Administration
Genome-wide association study
Human leukocyte antigen
Inflammatory bowel disease
International cancer genome consortium
King Abdulaziz City for science and technology
Knowledge, awareness, and practice
King Abdulaziz University
King Fahd Medical Research Center
Kinesin-13 super family protein 2A
Kingdom of Saudi Arabia
Next generation sequencing
Nature Publishing Group
Preimplantation genetic testing
Qatar National Research Fund
Single cell whole genome amplification
Standard operating procedures
The Cancer Genome Atlas
Telomerase reverse transcriptase
Telomere position effects
Telomere position effects over long distances
Whole genome sequencing
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The authors would like to express appreciation to the higher administration at King Abdulaziz University for their support of the meeting. The authors would like to thank all the technical staff at CEGMR. In addition, the authors would like to thank the CEGMR IT team led by Mrs. Reem for its tireless efforts in ensuring things were completed professionally and on time. The authors would like to thank Hamza Abu-Elmagd, School of Pharmacy, University of Reading, UK, for proofreading the manuscript. Lastly, the authors would like to thank all corporate sponsors of the conference.
This article has been published as part of BMC Genomics Volume 17 Supplement 9, 2016: Proceedings of the 3rd International Genomic Medicine Conference: genomics. The full contents of the supplement are available online at http://0-bmcgenomics.biomedcentral.com.brum.beds.ac.uk/articles/supplements/volume-17-supplement-9.
The publication fee is funded by the Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.
All authors contributed to the writing up and revision of the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Abu-Elmagd, M., Assidi, M., Dallol, A. et al. The Third International Genomic Medicine Conference (3rd IGMC, 2015): overall activities and outcome highlights. BMC Genomics 17, 747 (2016) doi:10.1186/s12864-016-3085-4
- Autism Spectrum Disorder
- Autism Spectrum Disorder
- Telomere Length
- Central Nervous System Tumour
- Klinefelter Syndrome