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BUFFALO, N.Y. Four hundred 8th-graders will take a first step toward understanding personalized medicine when they attend the third annual Genome Day on the Buffalo Niagara Medical Campus on March 9.

The University at Buffalo and Roswell Park Cancer Institute have teamed up to engage these budding scientists and researchers as part of a series of STEM events designed to raise awareness and pique student interest in pursuing careers in the science, technology, engineering and mathematics fields.

Buses arrive at 9:30 a.m. at Roswell Park, located at the corner of Elm and Carlton streets. A pep rally kicks off the event at 9:45 a.m. in the Hohn Auditorium with brief remarks to follow by Buffalo Mayor Byron Brown, Buffalo Public Schools (BPS) Superintendent Kriner Cash and leaders from Roswell and UBs New York State Center of Excellence in Bioinformatics and Life Sciences (CBLS).

Additionally, the Niagara Frontier Transportation Authority and Lamar Transit will recognize Desanay Nalls, a 10th grader at the Buffalo Academy of Visual and Performing Arts, who is this years winning designer of the STEM poster hanging in 10 NFTA bus shelters.

Following these remarks, graduate students and postdoctoral associates will lead small groups of students in DNA extraction and other hands-on learning activities. These include karyotyping for chromosomal differences, origami to model DNA structures and identifying genetic mutations by interpreting sequences from healthy cells and tumor cells.

Genome Day is a partnership of UBs CBLS; UBs Genome, the Environment and the Microbiome (GEM) Community of Excellence; the State University of New York; and Roswell Park; with the City of Buffalo and Buffalo Public Schools.

News media are welcome to attend Genome Day and the following additional events.

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Making it personal at the UB and Roswell Park-hosted Genome Day - UB News Center

Genome sequencing has taken off in recent years, and large-scale projects are leading the way. This review looks at efforts around the world.

Gene sequencing has proved its usefulness as adiagnostic and prognostic tool. Its use in the identification of BRCA1 mutations is already a gold standard in cancer research. Thanks to personalized medicine trends and collaborations between the industry and regulatory authorities, we could see whole genome sequencing (WGS) turning into a common practice faster than one could have originally expected.

The next generation sequencing (NGS) market, including but not limited to WGS, was valued at 4.6Bn in 2015 and is expected to reach 19Bn by 2020. Many private companies, such as Illumina, Roche, Life Technologies and Pacific Biosciences, are rushing into NGS to answer the rising sequencing needs.

Thanks to this competition, the technology has quickly improved in the past years. Nowadays, you can easily order a gene screening test from afew hundredto a few thousand dollars, dependingon the provider and what you are looking for.

The genomic sequence of a cytogenetically aberrant human cancer cell line

Back in 2003, the International Human Genome Sequencing Consortium kicked-off the genome analysis race by sequencing a complete human genome after years of worldwide collaboration and billions of investment. A few years later, the price of WGS reached $1,000.

According to Illumina, it is expected one day that whole genome sequencing will cost less than $100. On one hand, pocket NGS is not yet practical or economical. On theother hand, most available equipment is still quite expensive. For example, Illuminas NovaSeq 5000 costs around800,000and a NovaSeq 6000 reaches almost 1M.

New partnerships, like the one between23andMeandRochesGenentechin 2015, are trying to capitalize on the wealth of data: this partnership aims toobtainwhole genome sequencing data from 3,000 peoplewithParkinsons disease. (Fun Fact:Googleinvested in 23andMe and its co-founder married 23andMes CEO.)

However, sequencing genomes to generate data is only part of the job. Quality check, preprocessing of sequenced reads and mapping to a reference genome still require powerful computing facilities, efficient algorithms and obviously experienced staff. It is a time-consuming process.

Everybody talks about the $1,000 genome, but they dont talk about the $2,000 mapping problem behind the $1,000 genome, says Peter Tonellato, Professor of Biostatistics at the University of Wisconsin.

Moreover, WGS generates huge amounts of data, which poses a challenge fordata storage.

The Broad Institute in Cambridge, Massachusetts, said that during the month of October, it decoded the equivalent of one human genome every 32 minutes. That translated to about 200 terabytes of raw data. Even if that quantity is smaller than what is handled daily by internet companies, it exceeds anything biologists and hospitalshave ever dealt with.

Amazon and Google understand this need and already offer to keep a copy of any genome for 24 ($25) a year, which translates to roughly 0.02/GB per month, since a file is commonly between 100 and 400GB. In 2014, The National Cancer Institute said that it would pay18M ($19M)to move copies of the 2.6 petabyte Cancer Genome Atlas into the cloud.

Our birds eye view is that if I were to get lung cancer in the future, doctors are going to sequence my genome and my tumors genome, and then query them against a database of 50 million other genomes,said Deniz Kural, whose company, Seven Bridges, stores genome data using Amazons cloud system.

The UK was the first to launch a dedicated program to whole genome sequencing in Europe. Genomics England aims to sequence up to 100,000 whole genomes from patients with rare diseases, their families, and cancer patients from 11 Genomic Medicine Centres. Ten companies including GSK, AstraZeneca and Rochehave signed up to be part of the GENE Consortium, giving them access to 5,000 sequenced genomes.

Genomics England

These collaborations can raise concern regarding access to private health data, but there is no doubt that such a massive project could not be possible without private funding. Genomics Englands community management is impressive, with frequent updatesand campaigns to raise public awareness.According to a monthly updated counter, almost 20,000genomes have been sequenced so far!

On a similar framework, Australia is currently working on the 290M (AU$400M), 4-year100,000 Genomes Project (100KGP), sequencing patients with rare diseases and cancer to create a massive database for R&D.

Estoniaproposed an ambitious personalized medicine program in June 2000 and thus became an unexpected pioneer. The Estonian Genome Project Foundation aimed at collecting 100,000 randomly selected samplesbefore 2007. As of February 2014, the project had collected data from 52,000 adult donors including only a few hundred WGS.

In theUSA, the Precision Medicine Initiative (PMI), with its 1-million-volunteer health study, will gather a large database of health data including genetics and lifestyle factors. To make a long story short, the Mayo Clinic will analyze and store onemillion blood and DNA samples.

As in theUK, some of the anonymized data will be probably made available to researchers and industries in order to stimulate the project, which started in 2016 with 52M ($55M) from the NIH to build the foundational partnerships and infrastructure needed to launch theprogram.

In 2016, France announced the France Medecine Genomique 2025 program, aiming to open 12 sequencing centers and ensure235,000 WGS a year. TheFrench government is planning to inject 670Min this program, whose mainaim is to use WGS as a diagnostics tool.

Many other western countries such as Ireland and Iceland have launched their own programs. However, when, but when it comes to personalized medicine, take into account genetic variability between populations is a prerequisite. Western medicine has historically targeted western populations but, nowadays, western medicine is a worldwide practice.

There is a massive bias in medical research;Europeans have been developing drugs for Europeans without asking how compatible these pharmaceuticals are for the rest of the world. Stephan Schuster, Chair of the Genome Asia consortium.

Based on this observation, the non-profit consortiumGenomeAsia 100Kdecided to generate genomic data for Asian populations. Supporters of the initiative include genomics companies Macrogen inKorea and MedGenome inIndia, as well as Illumina. According to thePHGFoundation, at least 50,000 DNAsamples havealready been collected, and initial work will focus on creating suitable reference genome sequences for key populations in Malaysia, India, Japan or Thailand.

With the same purpose, the Qatar Genome Program aims to establish the Qatari Reference Genome Map by sequencing 3,000 whole genomes, which accounts for around 1% of the Qatari population.

Last but not least, China has been an unbeatable leader in genome sequencing for years now. In 2010, the BGIgenomics institutein Shenzhen was probably hosting a higher sequencing capacity than that of the entire United States. Chinas sequencing program is not just aiming for thousands but ratherone million human genomes and will include subgroups of 50,000 people, each with specific conditions such as cancer or metabolic disease. There will also be cohorts fromdifferent regions of China to look at the different genetic backgrounds of subpopulations.

It is difficult to anticipate the impact of WGS in modern medicine, but ethical issues regarding privacy of health data have already emerged. It is obvious that no one would like to see GAFA (Google, Apple, Facebook, Amazon) selling genome data as they are probablyalready doing with personal data from their users.

A key challenge is that ethical, legal, and social concerns raised by the most innovative technologies, including celland gene therapy as well as sequencing, significantly differ between regions. This definitely gives a certain advantage to countries with less restrictive laws, which areusually not western countries. For example, in Europe, transparency about the purpose of sample collection and protocols aremandatory before any research is conducted.

Although it is easier said than done, regulators should be proactive and set up an appropriate framework for these promising but challenging approaches while ensuring it does not hinder R&D.

Images via whiteMocca /Shutterstock; Clark MJ et al. (2010),PLoS Genet 6(1): e1000832; GenomicsEngland;National Institutes of Health

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The Past, Present and Future of Genome Sequencing - Labiotech.eu (blog)

Integrated DNA Technologies (IDT) is the first genomics company to develop and bring to market a complete ribonucleoprotein-based Cpf1 CRISPR system. The Alt-R A.s. Cpf1 CRISPR System inherits the optimised, efficient, and cost-effective traits of IDTs innovative Cas9-based system while taking advantage of Cpf1s natural AT-rich target sequence preference and ability to make staggered cuts. In addition, IDT is launching an associated range of CRISPR support tools to expand experimental options and capabilities for molecular biology researchers. The new tools extend the ease-of-use and performance of IDTs Alt-R system through options for fluorescent visualisation, enhanced nuclease transfection, and genome editing detection. Together, the new expanded Alt-R range breaks barriers to wider target spaces not addressable by Cas9 systems alone, and provides a level of flexibility in experimental design not previously possible.

IDTs Alt-R System already overcomes the limitations of using sgRNAs in the ribonucleoprotein (RNP) complex by enhancing editing efficiency and lowering toxicity. Now, in developing a complementary Cpf1-based system, IDT has opened up options for targeting AT-rich sequences. The new system includes the Alt-R A.s. Cpf1 nuclease, containing two integrated nuclear localisation sites, which complexes as an RNP with a minimal 41-44 nucleotide Alt-R CRISPR-Cpf1 crRNA. The system requires no tracrRNA, reducing potential reagent costs and experimental complexity.

The expanded range of Alt-R support tools now includes the Alt-R CRISPR-Cas9 tracrRNA5 ATTO 550, and Alt-R Electroporation Enhancers for Cas9 and Cpf1. The former allows in vivo fluorescent visualisation of the RNP complex and FACS enrichment of transfected cells without affecting RNP functionality, while the enhancers improve the efficiency of transfection using the Nucleofector (Lonza) and Neon (Thermo) electroporation systems. These new tools enable researchers to improve the overall efficiency of their genome editing over traditional methods. In addition, the new Alt-R Genome Editing Detection Kit provides a fast, easy, and low-cost method for confirming editing events with a T7 Endonuclease I (T7EI)-based mismatch detection system.

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Complete Cpf1-Based CRISPR Genome Editing System Available - Labmate Online