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Daily Archives: August 28, 2021
We may need to redefine ‘progress’ to find sustainability – Jackson Hole News&Guide
Posted: August 28, 2021 at 12:50 pm
Belief in progress is part of Americas cultural DNA. Each generation will do better than the last, with better understood in terms of rising income, bigger homes and more stuff. Sure, we have problems pollution, racial injustice, a pesky drought, fires on the horizon but Americans just get to work fixing those problems. To live in America is to reside on an ascending material curve.
I look out my window at the smoke that fills our valley. Later today I may go to town. Or not. The traffic discourages me from leaving the house. I need groceries, but when I walk into the store some shelves are empty; tourists have cleared them and there arent enough employees to keep things stocked. Id like to go for a hike in Death Canyon, but between the heat and the smoke and the traffic and the crowds on the trail I think Ill stay inside with my air purifier.
What has happened to our summers? It doesnt feel like things are getting better anymore. Visits to San Francisco or Boulder, Colorado, arent as much fun as they used to be. The New York Times recently described urban growth along the I-35 corridor between San Antonio and Austin as being a blur of subdivisions, commercial development and soul-crushing traffic, coalescing into a singular mass of population. Everything seems to be defined by excess: too expensive, too much traffic, too long a wait, too much heat.
Back in Jackson we should first acknowledge that a lot of this is outside our control. We cant stop the smoke or the drought, heat and fire that causes it. And the state of Wyoming wont let us put tollgates on the highways into town to limit access.
On the other hand, we arent resourceless. There are things we can do to improve our situation if we are willing to question our underlying assumptions.
In other words, theres a philosophical aspect to our difficulties. We say that we cant stop people from coming here. Its their right if they can afford the hotel prices. Its how we make our living. And how is Jackson going to progress if it doesnt continue to grow? Then we sit back and watch things spin further out of control.
Celebrate individual freedom and grow the economy: Its been the American definition of progress for a very long time.
Every culture is built upon a set of fundamental beliefs about what constitutes a proper (or acceptable, or meaningful) way of life. America was founded on open space, endless resources and constant technological innovation. There were so many resources that you could get yours without blocking others from doing the same. And if there was a problem wed just call in the scientists and engineers to invent a work-around. Our challenges were technical rather than political or philosophical in nature.
There is no technology, however, that will create more space in our valley. Building more roads to deal with traffic means that we will have to deal with the construction. Then traffic will get a little better for a while, which will encourage more people to come, which then increases the overall traffic. As for nature, we arent going to build new trails up Death Canyon. Even if we did that would mean a bigger parking lot below and even less of the solitude that we and the animals seek. The same is true in Denver and New Orleans: The solutions to our problems now often feed back into and worsen the problems that they were meant to solve.
There are no easy answers to our situation. But we can begin by questioning our dogmas.
We could take seriously the possibility that the way of life that worked for 300 years may need adjustment for the 21st century. We could adapt our ideals of freedom and opportunity to a world where space and resources are limited. We could challenge the assumption that more growth in Jackson equals a higher quality of life, and ask whether 1 million visitors to Yellowstone National Park in a single month is good for us, the visitors or the environment.
Jackson is a microcosm of our general situation: The American way of life will have to change. This might sound unpleasant. The very idea might make you angry. But cultures that do not adapt to changing conditions slide into decay.
For instance, it may seem painful to have to check our cars at the entrance to the parks or to give up our personal automobiles entirely. But such changes could lead to a way of life that is both more beautiful and more sustainable in the long run. Progress can be redefined in ways that are less materialistic, more inclusive, and easier on the environment.
Its worth considering.
Hoback resident Robert Frodeman writes on technology and the environment. He can be reached at robert.frodeman@gmail.com. Guest Shots are solely the opinion of their authors.
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We may need to redefine 'progress' to find sustainability - Jackson Hole News&Guide
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James Harden is making noticeable progress with his hamstring – Nets Wire
Posted: at 12:50 pm
Nine-time All-Star James Harden has always been known for his durability. You can count on him to always show up. The Beard has played in 657 regular season games since 2012 while averaging 36.9 MPG in that time period. In his first stint with the Nets coming from Houston, it was the first time Harden suffered from an injury both prior and during the postseason. This has now raised concerns on what to expect going into training camp.
Harden, of course, is still fully recovering from a hamstring strain which reached a grade 2 sprain in the playoffs. You can pinpoint this to some lack of conditioning at the start of the season or maybe age. Now at 32-years-old, all the minutes the Nets star has compiled since 2012 can be catching up.
Nevertheless, one thing is for sure, and that is that we are going to find out in the next couple of months when the season commences. Theres some good news though for Brooklyn. In a recent workout video, Hardens hamstring is making significant progress that isnt hard to notice:
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James Harden is making noticeable progress with his hamstring - Nets Wire
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Rantoul rolls out the welcome mat for Half Century of Progress show – Agri News
Posted: at 12:50 pm
RANTOUL, Ill. Just as the Half Century of Progress show is an opportunity for the owners of vintage tractors and other farm equipment to strut their stuff, so it is for the village of Rantoul.
We get to put our best foot forward. Champaign County gets to put its best foot forward, said Scott Eisenhauer, the village administrator of Rantoul.
Eisenhauers duties as village administrator include overseeing day-to-day operations, budget and financing and economic development for the village.
So, he recognizes not just the economic benefits that the Half Century of Progress show brings, but also the additional benefits that might not be measured in dollars and cents.
But the economic benefit itself is significant.
There is no question there is a significant economic advantage to it. When you bring that number of people into your community, they are buying gas, they are eating food, they are staying in hotels or at the campground. There is no question there is a revenue generation that benefits the community as a whole when we host this event, Eisenhauer said.
The dollars that participants in the show and visitors to the show spend in the community go back into the community.
Its good not only for the village financially, but also those are dollars that we can spend on other things to make the community better, which thereby benefits the residents, Eisenhauer said.
Dollars and economic activity are just one benefit that the four-day show, which draws participants and visitors from across the United States and even internationally, brings to Rantoul.
The other thing, though, that I think is just as critically important as the financial advantage and that is the ability for Rantoul, Illinois, to be in the national and, in some ways, the international spotlight for that week. Its a great opportunity for us, every two years, to promote our community, Eisenhauer said.
As the countdown to the show goes on, the village is putting the finishing touches on the welcome mat it will roll out for the show.
This is the lull before the storm. We are making sure that our resources are in place, that the things that we have the most involvement in, traffic patterns and parking, that those are all being addressed. We already have our recreation crew on the grounds, doing some work around the airport, getting grass cut and weeds cut and stumps ground and things like that, to make sure we have a nice, clean and visually appealing area, Eisenhauer said.
That recreation crew is deeply involved in preparing for the show and as the show gets ready to start.
The recreation department does a great job in preparing the grounds in advance of the show and then also setting up and providing resources to help with the set up process, Eisenhauer said.
Employees at the Rantoul Airport also have been busy getting ready for the show. The airport is maintained by the village.
The airport has been ramping up in going around and making sure the electric works and the lights work and those types of things are ready to go so when we hit that mark, the weekend before the show takes place, and they start moving onto the grounds, everything that we need to have done in preparation is finished, Eisenhauer said.
The planning process for the show is extensive.
The village is heavily involved in the planning process with the leadership of the Half Century of Progress show and particularly that deals with parking logistics and traffic logistics. Those are really two of the most prevalent areas, getting people into the show and then, once we get them to the show, getting them parked and ultimately getting them back out. That is a large task taken on by our police department, Eisenhauer said.
But the villages involvement in the show doesnt end as the tractors and other equipment roll onto part of the former Chanute Air Force Base.
During the show we also provide police involvement, security. Our fire department is present to provide fire response and we also work with other entities leading up to the show that have ancillary relationships with the show, Eisenhauer said.
An additional benefit comes in the form of the working relationship the village and village officials have with the leadership of the Half Century of Progress.
The incredible men and women that we get to work with, from John to Russell and everybody who serves on a committee for the show, they could take this show anywhere, but weve built that partnership, weve built that relationship. We believe in what they are doing and I think they believe in what we are willing to assist with in order to keep that show here in this community. We are so grateful, as a village and as a community, that the Half Century of Progress located here originally and continues to flourish here in the community. Its always fun to be around people who are passionate and dedicated to pulling together an event and well organized enough to make that happen, Eisenhauer said.
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Lakewood Ranch-area parents uncertain of how the school year will progress – YourObserver.com
Posted: at 12:50 pm
Lakewood Ranch's Elly Barr was ready to send her kids back to school for a somewhat normal school year.
Her daughter was entering seventh grade and her son was going into eighth grade at R. Dan Nolan Middle School. They were not planningto wear masks as the district started the year with an optional mask policy.
But then the number of cases among students and employees throughout the School District of Manatee County increased.
The first day of school Aug. 10, nine cases were reported. By the end of the first week, there were 179 cases in the district. Two weeks into school, the district reported 825 cases with 227 of those cases coming from schools in East County.
In the entirety of last year, East County schools reported 347 cases.
Now families are adjusting to the increase in COVID-19 protocols at school that the district hopes will mitigate the number of cases on campuses. With more cases, parents are uncertain of how the year will progress.
"All of a sudden it seemed to explode," Barr said. "It's very mental right now. If you don't wear a mask, it's like you don't care. If you do wear a mask, it's like you're being over protective of your child. It's been very judgmental. I don't actually know what to do for the best anymore. I'm just doing what I feel is right."
After the second day of school, Barr's daughter, Alice, was sent home to quarantine after possibly being exposed at school.
Barr now is sending her children to school wearing masks. With her eldest, who is a student at Lakewood Ranch High School, returning home after having a spinal fusion, she's worried someone will bring COVID-19 home and possibly spreading it among family members.
"I'm a bit nervous about that, so I'm taking care of my family as well," Barr said. "Everything just seems to have gone out of control. I don't know how it's looking for the future to be honest."
River Place's Nicole Hamer described the first two weeks of school as chaotic. She has two third graders at Braden River Elementary, a seventh grader at Braden River Middle and a freshman at Braden River High School.
Hamer said one of her sons already has been sent home to quarantine, and her seventh grader and freshman are having transportation issues due to the district's bus driver shortage.
"For my middle schooler, the bus has not comeand when it has come, it's been very late," Hamer said. "For my high schooler, they didn't even have enough room on his bus. They said the bus is full and we can come back in an hour and a half to get you."
Mike Barber, a spokesman for the district, said the district has 133 bus routes and in the weeks leading up to school, 20 drivers left the district to take other jobs. Then another 20 drivers had been out at different times during the first eight days of school for "health reasons."
Barber said everyone in the transportation department is certified to drive, so everyone in the office staff is driving buses to help with the shortage in drivers.
As for the increase in COVID-19 cases throughout the district, Hamer said she's not concerned because "it seems like almost everyone is going to get this, vaccinated or not."
"I don't really know how to feel," Hamer said. "I know a lot of people that have been vaccinated and have gotten it and have it right now. It's kind of hard to judge how I feel. I'm just kind of going with the flow."
Hamer isn't sending her kids to school with masks because she doesn't believe it's mentally healthy for her children. She's also had friends whose kids go to schools that require masks and their children still are being sent home to quarantine or are testing positive.
"I think everyone is doing the best they can," Hamer said. "I think it's just going to be a virus where people are going to have to build up their immune systems. I mean everybody's got a tough job. I can't comment anything negatively. I think everybody's doing a great job with what we're being dealt with."
Lakewood Ranch's Amy Hammon pulled her daughter from Robert E. Willis Elementary School last year because she wasn't doing well with e-learning, but she didn't want to send her to school because of COVID-19.
Kate Barlaug, the principal of Carlos E. Haile Middle School, helps a student navigate her way around campus. Photo courtesy of the School District of Manatee County.
Now, her children are attending Pinnacle Academy because they have a mandatory mask mandate in place that doesn't have an opt-out option until the positivity rate in the area is lower. She said the mask mandate makes her feel her children will be safe on campus.
"My children will continue to wear masks and take all precautions possible," Hammon said.
Although her children are in private school now, Hammon continues to write to the School Board of Manatee County, Gov. Ron DeSantis and Richard Corcoran, the commissioner of the Florida Department of Education, to advocate for everyone to wear masks in school.
"We have to fight for our children who are defenseless right now," Hammon said. "We are actually going to have to beg the state of Florida to allow our children to have the smallest sense of safety, which is a mask, because we have something that they don't and that is a vaccine. If we have the opportunity and have chosen to, we have been vaccinated. My family has been vaccinated. If my children were older, they would be vaccinated. Essentially, we are sending our children to school unprotected."
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Lakewood Ranch-area parents uncertain of how the school year will progress - YourObserver.com
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Equality is a work in progress – Minneapolis Star Tribune
Posted: at 12:50 pm
As the 101st anniversary of American women's right to vote is celebrated on Thursday, it's a good time to reflect on the past, present and future of gender equity.
Congress designated Aug. 26 as Women's Equality Day in 1973 to commemorate the 1920 certification of the 19th Amendment. Even though it wasn't until years later that women of color were effectively included, the day has become a marker to honor women's suffrage and remember the barriers females still face.
It's a time to think about the countless contributions women have made over the decades to turn the dream of equality into reality; about women who were not necessarily well known but who helped advance the cause. Many of those women's stories are told in the current Minnesota Historical Society exhibit "Extraordinary Women.'' It includes information about:
Katie McWatt, the educator and civil rights activist whose 1964 campaign for St. Paul City Council broke through race and gender barriers for city campaigns.
Sarah Burger Stearns, who petitioned to have the word "male'' struck from the Minnesota Constitution's definition of eligible voters in 1860s.
Marie Bottineau Baldwin, of the Turtle Mountain Band of Chippewa Indians, who helped handle legal cases for Ojibwe people in Minnesota and North Dakota. In the 1890s she moved to Washington, D.C., earned her law degree and joined the fight for treaty rights and tribal sovereignty.
Though we can celebrate the achievements of these women and others who paved the way for the progress enjoyed in the 21st century, we must also remember that more remains to be done. The goal of full gender equity has yet to be realized, either in the U.S. or globally. And, of course, women around the world lack many of the rights American women enjoy.
Today, the earnings difference between males and females still affects women's economic power, and gender-based discrimination still occurs in workplaces and business transactions. In 2020, women earned 84% of what men earned in the U.S., according to a Pew Research Center analysis, a figure that has remained the same for the last 15 years.
And though the Equal Rights Amendment (ERA) was introduced in 1923, but not heard in Congress until the 1970s, it took until 2020 for the required 38 states to vote for ratification. It still awaits official adoption because the U.S. House voted to eliminate the deadline for passage in the original legislation, but similar language is pending in the Senate.
Then there are the current attacks on voting rights that would ban drive-through voting, limit voting hours, make absentee voting more difficult and empower partisan poll watchers. Those changes could have a disproportionately negative impact on elderly and low-income women and on women of color.
While it's important to remember the advances of the past century, it's also essential to understand that women's equal rights are a work in progress. One of the best ways to celebrate and honor those who brought us thus far is to continue the struggle for gender equity and fairness throughout every sector of society.
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Crews Continue Making Progress on Wildfires Across Northwest Montana – Flathead Beacon
Posted: at 12:50 pm
Thanks to a stretch of highly welcomed cooler and moister weather in recent weeks, crews have made significant progress on wildfires in Northwest Montana, allowing authorities to lift evacuation orders and further establish containment lines from Thompson Falls to Polebridge to Troy.
Even with the moderate conditions, fire and land managers remind the public that Stage 2 fire restrictions are still in place throughout the region. Those restrictions include a prohibition on campfires. For more information, visit http://www.mtfireinfo.org.
Evacuation warnings issued in late July for the lightning-caused Hay Creek Fire near Polebridge were lifted on Aug. 18 amid cooler temperatures and higher humidity. The Type 3 incident management team overseeing attack operations transitioned to a local Type 4 incident command from the Flathead National Forest on Aug. 21.
The fire was 2,894 acres and at 60% containment late last week, according to an incident report update.
The lightning-caused Thorne Creek Fire near Thompson Falls, the states fourth largest at 39,053 acres, was at 80% containment following an infrared flight over the weekend that resulted in a significant increase in containment, according to an incident report.
Saturdays rain kept fire activity to a minimum which allowed firefighters to secure most of the fireline, bringing containment to 80 percent, the report states.
The Thorne Creek Fire initially forced evacuation orders for more than 200 residents in late July, but the Aug. 23 update noted that the Thompson River Zone is now in pre-evacuation status and open to residents only. No structures have been lost.
The Southern Area Gold Team planned to transfer command of the Thorne Creek Fire back to the Lolo National Forest on Aug. 25 at 7 p.m.
Over the weekend, crews finished a direct line on the northwestern corner of the 12,522-acre South Yaak Fire, located near Troy, increasing total containment to more than 60%, according to an Aug. 23 update. The nearby Burnt Creek Fire was burning at 4,066 acres and 29% containment on Monday.
No updated incident reports for the Boulder 2700 Fire on the east shore of Flathead Lake have been posted since Aug. 16, although crews were making ample progress and evacuation orders had been lifted. The fire leveled more than 20 structures when it grew abruptly under warm winds on the night of July 31.
The Confederated Salish and Kootenai Tribes Division of Fire has shifted its regular updates from the Boulder 2700 Fire to the Crooks Fire burning 10 miles east of Arlee.
According to an Aug. 22 update, the Crooks Fire was 3,258 acres at 0% containment, with 147 personnel attacking the blaze. No structures were threatened at that time, and no evacuation orders were in place.
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Genetics and Human Genetics | Graduate School
Posted: at 12:49 pm
The Department of Genetics and Human Genetics offers courses leading to the Master of Science and Doctor of Philosophy degrees . The program is associated with the Departments of Pediatrics and Biology so that students will not only learn to work creatively in their own field of special interest but will also be able to relate their findings to progress made in related disciplines.
The graduate programs in Genetics & Human Genetics are designed to confer the training standards that will develop students for degrees of Doctorate of Philosophy Masters, and M.D./Ph.D. degree(s). The graduate program is an interdepartmental entity built on a diverse platform.
The program is associated with the department of Pediatrics and department of Biology where students work creatively in their field of special interest but and be able to relate application and relevance to related clinical and science disciplines.
The degree programs are designed to provide a curricular foundation in human genetics for all enrolled students during their first year.Following this, guided by their academic adviser, students elect to pursue their area of interest in genetics . This is accomplished through a combination of elective courses offered in the Department and other departments of the University, as well as in the Washington Area Consortium of Universities. The Masters thesis and Doctoral dissertation research interests likewise can reflect a broad range of interests, provided a suitable research mentor is identified in the graduate faculty.
This training program design takes into account the fact that genetics is increasingly relevant within the framework of multiple biomedical research and scholarly pursuits. The program design also is intended to foster the important principle of collaborative research and scholarship among biomedical disiplines.
The graduate programs are research-oriented curriculum's in the study of genetic mechanisms related to the transition from normal to disease states and intended to prepare graduates to participate in laboratory research.
To be accepted into the Graduate Program in Genetics and Human Genetics, students must have a Bachelors degree from an accredited institution and a GPA of at least 3.0 or B equivalent. In addition, students must meet the University requirement(s) to take the Graduate Record Examination (and the TOEFL if applicable).
Students with a bachelor degree may enter the graduate program at the Masters level or directly into the Ph.D. program. Eligibility to be considered for direct admission as a Ph.D. student requires a cumulative GPA greater than 3.2 and prior research and/or training experience in during undergraduate school or during a previous Masters degree
Applicants are required to submit these items for consideration of acceptance and review of potential for success:
Students wishing to enter the master's program should have a baccalaureate degree and a cumulative GPA average of B or the equivalent. They also should have completed undergraduate courses in modern biology, chemistry through organic chemistry, general biochemistry, mathematics through calculus, and general genetics, or equivalent courses. These prerequisites apply regardless of specialization selected within the master's program.
Students with less than a B average or who have not completed all of the required undergraduate courses may be admitted conditionally if they have very high Graduate Record Examination scores and/or excellent recommendations.
Students may matriculate into the doctoral program, having completed a suitable Masters degree, provided they present evidence of previous research experience supported by excellent letters of recommendation, and grades above 3.2 average.
Students who do not meet these general criteria may be considered for the master's program as indicated above.
CORE COURSES AND COURSE OFFERINGS
Fall semester ( yr 1)
Spring semester (yr 1)
Fall Semester (yr 2)
Spring Semester (yr 2)
GENETIGENETICS AND HUMAN GENETICS COURSE DESCRIPTIONS
Intro to Biochemical Genetics 219 (6cr) Fall only (MWF) - This 6-credit course is designed as an introductory course in biochemistry with special emphasis on those areas of biochemistry that are especially relevant to genetics and human genetics. The course is team-taught using faculty members and guest lecturers who have particular interest or training in each topic to be covered. The course is organized around four major units: Proteins and Enzymes, Nucleic Acids, Hormones, and Metabolism. The course is designed to develop a students; recall of cellular biochemistry, knowledge base of the relationship between the genetic code and the translation of biochemical pathways in disease pathology, comprehension of the relationship between pathological genetic changes to the biological process that cause human disorders.
Research in Genetics 220 GC (1-9cr). This course provides academic credit for independent research. It is offered on a variable credit basis and students may elect to register for 1 to 9 credits, depending on the level of time commitment to research the student expects to dedicate. In most cases, the research conducted in this venue is research under the guidance of a faculty mentor of the students choosing leading to a masters thesis or doctoral dissertation. This course is structured so that Masters and Doctoral students can focus on and perform literature research, identify mentors & research projects, and conduct thesis and dissertation research in the Department of Genetics & Human Genetics. Because research is rarely completed in a single semester, this course may be taken repeatedly until the research is concluded and the thesis or dissertation judged to have passed.
Hum Biochemistry & Molecular Gene 222 (4cr). This course explores the biochemical characteristics of variation in human genetic material and in corresponding gene products. This requires integrating information on gene structure, regulation of gene expression, gene product, and the physiological/anatomical phenotypes which reflect mutations. This course addresses concepts of intragenic repetitive sequences, DNA methylation, imprinting, genetic heterogeneity as it relates to genotype-phenotype correlation. The molecular evolution of specific genes are explored through both orthologous and paralogous sequence homologies. The goals of the course is to develop familiarity with a sample of genetic disorders distributed over various human anatomic, biochemical, and physiological systems, develop skills in integrating inherited abnormalities in molecular and biochemical structures as rational explanations for selected phenotypes. The format of the course consists of lectures by a spectrum of clinicians and researchers who have a high degree of familiarity with their subject matter.
Human Genetics I 223 GC (3cr) Fall only. The course is distributed over two semesters as Human Genetics I & II. This course offers a careful study of the conceptual terrain for the discipline to develop a working familiarity with many of the central concepts in contemporary human genetics, recognize the roles of technology and human values in shaping the central concepts, develop proficiency in analyzing models of heritable variation and corresponding phenotypic expression, and their distributions in pedigrees and populations, and to identify evidence for interactions between gene expressions and environment to yield phenotypes. The course format combines lecture, discussion, assigned readings to provide further content depth and breadth.
Human Genetics II 224 (3cr) This course is a continuation of Human Genetics I. This course will cover a minimum of 30 multifactorial phenotypes (congenital malformations and late onset disorders). This course distinguishes and characterizes each of the models of inheritance as it pertains to relationships between genes and phenotype. Its designed to cover principles of multifactorial or polygenic models for estimating empiric recurrence probabilities, correlations between genetic and environmental factors of phenotypic value and heritabilities. One goal is to identify the spectrum of approaches currently envisioned for medical intervention in genetic disorders.
Cytogenetics 229 (3cr). This course is designed to develop a basic understanding of cytogenetics. The course covers chromosomal abnormalities and the etiology of how chromosomal aberrations contribute to congenital disease and cancer. The course will provide in-depth content and focus on cytogenetic and molecular cytogenetic diagnostic techniques. The goal of this course is to have students become proficient in preparing detailed genetic counseling case studies.
Seminar in Genetics 229 (2cr). This course is offered each semester and current residents are invited to register continuously. Course format involves student participation in group discussion and article presentation each class period. The course is designed to focus on acquiring familiarity with current research in basic, clinical, and translational genetic disorders presented in various peer reviewed journals. The format promotes developing skillsets for; gathering, organizing, validating, and interpreting data of peer reviewed articles in molecular, biochemical, clinical, and population genetics. Students will develop the knowledge base to identify and compare the quality of molecular techniques and analytical tools used to perform research. The goal is to acquire skills to employ information from peered reviewed publications as a guide to understanding molecular evolution and forming individual research hypothesis.
Introduction to Medical Genetics 231 (3cr) This course introduces students to the clinical aspect of a broad range of human genetic disorders, focusing on phenotypic characteristics, current confirmatory diagnostic techniques for each disorder, and approaches to interventions in terms of either prevention of occurrence, reduced morbidity, or achieving improved coping with disease. The course is designed to develop a students ability to construct pedigrees and to interpret modes of inheritance. Course formats consists lectures organized in a case study format such that an integration of all components of phenotype can be understood in relation to rationale for diagnostic methodology, and relevant intervention approaches. Students perform assigned reading, on-line searches on genetic diseases.
Intro to Research in Genetics 233 (3cr) This course is required for all Masters and Ph.D. students in the first year. The course is designed for development of a hypothetical research project and writing of a detailed research proposal as a semester-long exercise. The course objective is to acquaint the student with a multitude of issues that bear on the successful conduct of independent research which include; understanding how to conduct literature searches, development of a hypothesis, identification of specific aims that will test the hypothesis, experimental design using principles of the scientific method, preparation and presentation of a written research proposal. This exercise will prepare the student for developing a thesis or dissertation proposal.
Gene Structure & Action 236 (2cr). This course explores the molecular process by which the synthesis, expression, and manipulation of genetic material is organized in chromatin and in cis-acting elements governing the process of the central dogma. It will include a critical review of gene organization, regulation of gene expression by hormones, growth factors, and oxidant stress emphasizing signal transduction pathways and the action of ligand-receptor mediated transcription regulators. Attention will be paid to regulation of gene expression, transcription, and translation by RNA interference and natural & synthetic xenobiotics. The goal of this course os to understand the nature and function of gene expression in proliferation, differentiation, and apoptosis in development and disease.
Psychosocial Aspects of Gene Disorders 312 (3cr) Analyzes psychosocial consequences of genetic disorders for each member of the family, impacts on life plan, decision-making, coping strategies, and approaches to counseling for such psychosocial consequences. Case studies are included together with development of skills in psychosocial interviewing and pedigree construction. Enrollment is limited.
Ethical, Legal, Social Issues in Medicine 313 (3cr) This course introduces students to ethical and bioethical issues confronting healthcare providers in the context of health care delivery and research. Students are introduced to the main theories and principles of bioethics and the moral foundations of patient-provider relationships, professionalism, relevant ethical and legal considerations and the concepts of moral reasoning. By utilizing the Bebeau Grid method to collect and analyze case information, students to develop the critical thinking skills necessary to identify and analyze ethical dilemmas and to construct well-reasoned responses to the dilemmas and resolving case material presented in the small group class sessions.
Cancer Genetics I: Clinical Aspects of Cancer 315 (3cr). This advanced elective course focuses on the genetics of cancer, specifically clinical aspects of cancer. Course format follows two hours of didactic lectures with one hour of an active learning component, bioinformatics and labs. This course will provoke dialogue by engaging class participation in questions & answers, as well as targeted discussions of information on the lecture topic gathered from other resources. The course is designed as a valuable resource for mainly graduate and health professional trainees, with interests in genetics and clinical cancer genetics. This course serves as a prerequisite to Cancer Genetics II: Molecular Aspects of Cancer.
Mutation Human Genes 412 (2cr). This course is structured for research ideas and current advances in genetic and biochemical alterations as a tool for clinical and translation research. This entails an integration of current events and data into the learning modality that utilizes current peer reviewed journal articles. This course focuses on using the substantial array of literature and bioinformatics to develop skills for analyzing data and addressing concepts of interpretation of data. Current peer reviewed publications are the materials used to generate an active learning education that supports group teaching, individual communication, and development of analytic skills. Course format is seminar based where students will present a 2-3 page written summary on the topic covering the molecular lesion, biochemical pathology, and a specific clinical disease associated with the genetic mutation of topic.
SPECIALIZED TRAINING COLLABORATIONS:
National Human Genome Center
As the only research center of its kind at a predominantly African American university, the National Human Genome Center (NHGC) is singular in its capacity to provide leadership for America and the global community in genetic studies of diseases common in African Americans and other people of color throughout the African Diaspora. In concert with the mission of Howard University, particular emphasis at the NHGC is placed on providing education opportunities of exceptional quality for African Americans and other historically disenfranchised groups. The NHGC is also dedicated to attracting, sustaining, and developing a cadre of research scientists, who through their investigations, are committed to reducing health disparities among ethnic groups, preventing disease and promoting health.
The National Human Genome Center (NHGC) Molecular Genetics Training Program accepts and supports promising students who seek research training in molecular genetics, genomics, and related clinical fields. The overall goal of these programs is to promote interdisciplinary, collaborative and innovative research training in areas relevant to the mission of the National Human Genome Center at Howard University.
The NHGC is a strong, valuable, and supportive center for supervising, training, and developing the professional scholarship if residents of the Genetics & Human Genetics department.
Research Center in Minority Institutions (RCMI)
The RCMI Program focuses on the enhancement and further development of the necessary research infrastructure which will ensure the Universitys ability to contribute to the investigation of diseases and provide collaborative consolidation of instrumentation, technical expertise, and support personnel to enhance the impact and availability. These research infrastructure components include the expansion of two research core laboratories: The Laboratory of Molecular Computations and Bioinformatics (LMCB), the Proteiomics Core Facility and the Biomedical NMR Laboratory (BNMR).
New efforts and programs are being developed to train Genetics students in bioinformatics and computational biology.
Sickle Cell Disease Center
The Center is committed to a six-fold goal that includes comprehensive medical care, research, testing, education, counseling, and community outreach. Recently, the Center has expanded its clinical research program and developed a collaborative consortium with Childrens National Medical Center (CNMC) and in working together with Howard University Hospital and NIH.
The Center has a long history of major participation and leadership in national and international research projects that have led to the development of effective therapies for sickle cell disease. With many of the basic molecular issues in sickle cell disease being better understood, major research efforts now focus primarily on clinical issues such as treatment for the disease.
The Center for Sickle Cell Disease offers clinical services and patient care:
The Center for sickle cell disease has trained Genetics students in research-intensive thesis and dissertation projects that have produced scholarly work.
http://www.sicklecell.howard.edu/
Cancer Center
Howard University Cancer Center (HUCC) is our natural ability and strength to address cancer disparities with an emphasis on those cancers that disproportionately impact African-Americans, in particular. There are three overarching programmatic areas in the Cancer Center: (1) cancer biology; (2) cancer etiology; and (3) cancer prevention, control, and population sciences; whereby cancer disparities represent the underlying theme of the research focus.
The ultimate goal of the Cancer Biology Program is to translate basic laboratory results from the bench to the bedside. Research activities that are currently underway in the cancer biology program include the following: (1) prostate cancer genetics; (2) methylation profiling and risk of colorectal cancer; (3) differential transcription factor activation of H. pylori; (4) triple negative breast cancer in young African-American women; (5) nicotine, biogenic amines and depression; and (6) in vivo NMR spectroscopy for noninvasive pharmacokinetics.
The Cancer Etiology Program focuses on epidemiologic research among predominantly African-Americans and underserved populations. This program examines risk factors that increase or decrease the likelihood of developing cancer risk and its precursors.
The Cancer Prevention, Control and Population Science Programs goal is to reduce the burden of cancer measured by incidence, morbidity, and mortality utilizing behavioral and clinical research interventions.
The department of Genetics and Human Genetics and the Division of Medical Genetics have faculty in the Cancer center that assist in the training and prospectus documents of our Ph.D., masters, and masters in counseling students.
http://cancer.howard.edu/about/overview.htm
The steps in the application process are as follows:
The application for the M.D./Ph.D. program should be returned to:
Kareem Washington, Ph.D.Director M.D./Ph.D. ProgramHoward University College of Medicine520 W Street, NWWashington, DC 20059email:kareem.washington @howard.edu
A student, with the advice of the director of graduate studies, may file for admission to candidacy.
Students in the Ph.D. program are required to spend at least three semesters in full-time residence, two of which must be consecutive.
Assistant Professor
Principal Invetsigator
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Genetics and Human Genetics | Graduate School
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Postdoctoral position with combined wet and dry lab work at the – Nature.com
Posted: at 12:49 pm
The University Hospital Heidelberg is one of the major healthcare centers in Germany. Our objective is the development of innovative diagnostics and therapies as well as their quick implementation for the patient. With about 10,700 employees in more than 50 specialized clinical departments with almost 2,000 beds, about 80,000 patients in part-time and full-time inpatient treatment as well as 1,000,000 patients in ambulant treatment are medicated each year.
Postdoctoral position with combined wet and dry lab work at the Institute of Human Genetics (m/f/d)
JobID: P0025V441
at the earliest possible date searched for, AG Laugsch at the Institute of Human Genetics.
We are looking for an enthusiastic postdoc to join our research group at the Institute of Human Genetics of the University of Heidelberg. The position is limited to 3 years, with the option of further extension. The salary is based on TV-L salary groups.
Our laboratory explores the relationship between the head (craniofacial structures) and brain development in health and disease. We focus on developmental genes specifically and dynamically regulated, e.g., by enhancers. That regulation ensures the establishment of precise gene expression patterns during development, which might have pathological consequences when being disrupted.
Composed of international and multi-disciplinary scientists, our group creates a unique and inspiring environment and supports individual career development. For more information visit:
https://www.klinikum.uni-heidelberg.de/humangenetik/forschung/abt-humangenetik/ag-laugsch
(Magdalena Laugsch et al., Cell Stem Cell. 2019 May 2nd; Modelling the pathological longe-range regulatory effects of human structural variation with patient-specific hiPSC.;24(5):736-752)
Tasks and responsibilities
Creating and analyzing next-generation sequencing data, the successfull applicant will investigate the impact of cohesin on neural crest cells (hNCC) development and their contribution to Cornelia de Lange Syndrome (CdLS).
This rare but severe genetic disorder is caused by mutations in the cohesin complex or and its auxiliary factors and characterized by craniofacial and limbs malformations, heart defects, and cognitive deficits. Cohesin regulates the three-dimensional (3D) structure of chromatin and impacts the regulation of gene transcription. A large set of craniofacial abnormalities observed in CdLS patients most likely arises during the embryonic development of the hNCC. Hence, the postdoc will investigate the underlying molecular defects in hNCC derived from human induced pluripotent stem cells (hiPSC).
Combining genetic, epigenetic, and bioinformatic tools (hiPSC culture, CRISPR/Cas9 targeting, hNCC differentiation, RNA- and scRNA-seq, Hi-ChIP-seq, ATAC-seq, and analysis using advanced bioinformatics), the scientist will identify the 3D structure of chromatin and regulatory networks controlled by cohesin.
Your Profile
Ability to analyze your own data and significant proficiency as well as strong interest in Python, R, shell scripting and working with NGS data.
We offer
The application must include your motivation, a brief statement of your scientific interests, contact details from three references, curriculum vitae, separated publication list, and relevant certificates.
Please forward your complete application (in a single pdf document Filename: P0025V441_First Name_Second Name No other format will be accepted) by email.
Universittsklinikum Heidelberg
Institut fr Humangenetik
Dr. rer. nat. Magdalena Laugsch, Group Leader
Im Neuenheimer Feld 366
69120 Heidelberg
phone: +49 6221 56-39128
magdalena.laugsch@uni-heidelberg.de
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Postdoctoral position with combined wet and dry lab work at the - Nature.com
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Ulcerative Colitis Study Analyzes Gene Expression to Measure Risk of Progression to Surgery – GenomeWeb
Posted: at 12:49 pm
NEW YORK An international team of researchers has used transcriptomic data from ulcerative colitispatients to develop a predicted polygenic transcriptional risk score, or PPTRS,that can identify UC-affected individuals at fivefold elevated risk of progressing to surgical resection of the large bowel.
In a paper published on Thursday in the American Journal of Human Genetics, the Georgia Institute of Technology-led team noted that 5 percent to 10 percent of people with UC require bowel resection, or colectomy, within five years of diagnosis, but that polygenic risk scores based on genome-wide association studies generally don't provide meaningful prediction of progression to surgery. However, studies of Crohn's disease have shown that gene expression profiling of GWAS-significant genes provides some stratification of risk of progression to complicated disease through transcriptional risk scoring, or TRS.
In their paper, the researchers demonstrated that a measured TRS based on bulk rectal gene expression in a cohort of UC patients had a positive predictive value approaching 50 percent for colectomy. Single-cell profiling demonstrated that the disease-associated genes were active in multiple diverse cell types from both the epithelial and immune compartments, and expression quantitative trait locusanalysis identified genes with differential effects at baseline and the one-year follow-up, the researchers said. But for the most part, they found that differential expression associated with colectomy risk was independent of local genetic regulation.
Overall, their data suggested that prediction of gene expression from relatively small transcriptome datasets can be used in conjunction with transcriptome-wide association studies for stratification of risk of disease complications.
The researchers began by performing differential expression analysis between baseline rectal RNA-seq biopsies of individuals in the PROTECT multicenter pediatric inception cohort study of response to standardized colitis therapy. Analyses were done on 21 affected individuals who progressed to colectomy and 310 who did not. They identified downregulation of 783 transcripts in the individuals who underwent colectomy and upregulation of 1,405 transcripts overall.
They also obtained rectal biopsy RNA-seq data for 92 affected individuals at week 52 and observed a marked shift in gene expression at follow-up, prompting them to ask whether local regulation of the gene expression might contribute to this effect. They found that there were 72 SNPs that were significantly regulating 308 genes at both time points.
Further examination of the expression of colectomy-associated genes in a single-cell RNA-seq dataset obtained from rectal biopsies provided strong evidence that both epithelial and immune cells contributed to the risk of disease progression, the researchers said.
The researchers then performed a TWAS to capture the effects of all polymorphisms within 1 Mb of each transcript expressed in the PROTECT rectal biopsies and then used the weights to predict gene expression in a validation cohort from the UK Biobank. They tested for differential predicted gene expression in 70 percent of the validation samples and discovered about 800 genes either upregulated or downregulated in UC-affected individuals relative to non-IBD control individuals. They then derived a PPTRS for UC based on the effect sizes of the minor alleles and applied it to the remaining 30 percent of the validation samples, as well as to the PROTECT genotypes, and found that the PPTRS efficiently discriminated UC-affected individuals from non-IBD control individuals.
Significantly, it also discriminated the individuals who underwent colectomy versus those who didn't in both the UK Biobank and PROTECT.
"More extensive single-cell profiling, combined with cell-type-specific genetic analysis of gene expression, is likely to lead to the development of even better transcriptional risk signatures," the authors concluded. "It is also likely that such focused and personalized analysis may highlight specific pathological mechanisms active in particular affected individuals."
They did note, however, that these results were limited by the relatively small sample size of colectomies in the PROTECT study, and that validation of cross-ancestry assessments and the evaluation of the consistency of gene expression prediction across populations should be a high priority.
In an email, corresponding author and GIT researcher Greg Gibson noted that while the study's multiple layers of replication show that transcriptional profiling of the rectum greatly enhances risk stratification for risk of colectomy, this was not a clinical trial, so the approach is not yet approved for evaluation of patients.
"We hope that it will progress to implementation in the near future," he added."The prediction from genotypes alone is less likely to have clinical utility since the precision is still quite low, so that aspect is more research oriented."
He further noted that the approach he and his colleagues used could also be applied to a wide range of diseases, and that they are pursuing that research.
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Bionano Genomics Announces ESHG Lineup Featuring 11 Customer Presentations of OGM Data Spanning Three Major Clinical Research Areas of Application…
Posted: at 12:49 pm
SAN DIEGO, Aug. 26, 2021 (GLOBE NEWSWIRE) -- Bionano Genomics, Inc. (Nasdaq: BNGO) today announced the European Society of Human Genetics (ESHG) conference lineup featuring 11 customer presentations of optical genome mapping (OGM) data spanning three major clinical areas of application from 10 institutions and six countries. The clinical application areas represented below cover hematological malignancies, inherited genetic disorders and solid tumor analysis. The presentations are expected to cover the clinical utility of OGM across these application areas, along with the unique capabilities of Bionanos Saphyr system to detect all classes of structural variants, across the genome, at a superior resolution relative to traditional techniques. The ESHG conference is being held virtually starting this Saturday from August 28 - 31, 2021.
More than 3,400 participants are registered for this years ESHG meeting, which provides a platform for the dissemination of the most exciting advancements in the field of human genetics. The upcoming customer presentations featuring OGM data are listed below along with the associated clinical areas of application:
OGM Application Area
Presenter
Affiliation
Presentation/Poster Title
Hematological Malignancies
Dr. Anna Puiggros
Hospital del Mar, Barcelona, Spain
Analysis of genomic complexity in patients with chronic lymphocytic leukemia (CLL) using optical genome mapping
Dr. Jonathan L. Lhmann
Hannover Medical School, Hannover, Germany
The clinical utility of optical genome mapping for the assessment of genomic aberrations in acute lymphoblastic leukemia
Inherited Genetic Disorders
Dr. Caroline Schluth-Bolard
Universite Hospital de Lyon, France
What is the best solution to manage failures of chromosomal structural variations detection by short-read strategy?
Dr. Kornelia Neveling
Radboud University Medical Centre, Netherlands
Long-read technologies identify a hidden inverted duplication in a family with choroideremia
Dr. Valrie Race
Univ. Hosp. of Leuven, Leuven, Belgium
Bionano optical genome mapping and southern blot analysis for FSHD detection
Dr. Romain Nicolle
Hospital Necker-Enfants Malades, Paris, France
16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by Bionano optical genome mapping and WGS
Dr. Jenny Schiller
MVZ Martinsried, Martinsried, Germany
Characterization of breakpoint regions of apparently balanced translocations by optical genome mapping
Dr. Viola Alesi
Bambino Ges Children's Hospital, Rome, Italy,
Optical Genome Mapping: where molecular techniques give up
Dr. Valeria Orlando
Bambino Ges Children's Hospital, Rome, Italy
Optical genome mapping: a cytogenetic revolution
Solid Tumor Analysis
Dr. Florentine Scharf
Medical Genetics Center Munich, Germany
Germline chromothripsis of the APC locus in a patient with adenomatous polyposis
Dr. Mariangela Sabatella
Princess Maxima Center for Pediatric Oncology, Utrecht, Netherlands
Optical Genome Mapping Identifies Germline Retrotransportation Insertion in SMARCB1 in Two Siblings with Atypical Teratoid Rhabdoid Tumor
We believe our progress in Europe, with the increased awareness of OGM and the development of the market there, has been outstanding, commented Erik Holmlin, PhD, CEO of Bionano Genomics. Thanks to key sites like Radboud, Leuven and Cochin, the OGM footprint has now expanded in Germany, Spain and Italy. With the growing installed base of Saphyr in Europe, we have seen these institutions and their research teams conduct ground-breaking research to help demonstrate the potential utility of OGM as an alternative to traditional cytogenetics methods for the identification of genome structural variations that can be more sensitive, give a faster time to results and be less expensive to implement when compared to traditional methods. We believe the momentum of research that has been building will continue as more supporting data, like the data that we expect the researchers to show this week at ESHG, are released from around the world.
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For more details and to register for this online event please go to https://vmx.m-anage.com/home/release/eshg2021/en-GB
About Bionano Genomics
Bionano is a genome analysis company providing tools and services based on its Saphyr system to scientists and clinicians conducting genetic research and patient testing, and providing diagnostic testing for those with autism spectrum disorder (ASD) and other neurodevelopmental disabilities through its Lineagen business. Bionanos Saphyr system is a research use only platform for ultra-sensitive and ultra-specific structural variation detection that enables researchers and clinicians to accelerate the search for new diagnostics and therapeutic targets and to streamline the study of changes in chromosomes, which is known as cytogenetics. The Saphyr system is comprised of an instrument, chip consumables, reagents and a suite of data analysis tools. Bionano provides genome analysis services to provide access to data generated by the Saphyr system for researchers who prefer not to adopt the Saphyr system in their labs. Lineagen has been providing genetic testing services to families and their healthcare providers for over nine years and has performed over 65,000 tests for those with neurodevelopmental concerns. For more information, visit http://www.bionanogenomics.com or http://www.lineagen.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as may, will, expect, plan, anticipate, estimate, intend and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) convey uncertainty of future events or outcomes and are intended to identify these forward-looking statements. Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things: the timing, content and significance of the presentations identified in this press release; our assessments regarding our progress in the European market, including our expectations with respect to the continued adoption of OGM throughout Europe; the benefits of OGM relative to traditional cytogenetic testing methods and its potential to replace traditional cytogenetic methods; our assessments regarding current and future research by the institutions identified in this press release; and the execution of Bionanos strategy. Each of these forward-looking statements involves risks and uncertainties. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. Factors that may cause such a difference include the risks and uncertainties associated with: potential inaccuracies in presentations given at the ESHG Conference or subsequently published data that may minimize the impact of OGM in human genetics; the impact of the COVID-19 pandemic on our business and the global economy; general market conditions; changes in the competitive landscape and the introduction of competitive products; changes in our strategic and commercial plans; our ability to obtain sufficient financing to fund our strategic plans and commercialization efforts; the ability of medical and research institutions to obtain funding to support adoption or continued use of our technologies; the loss of key members of management and our commercial team; and the risks and uncertainties associated with our business and financial condition in general, including the risks and uncertainties described in our filings with the Securities and Exchange Commission, including, without limitation, our Annual Report on Form 10-K for the year ended December 31, 2020 and in other filings subsequently made by us with the Securities and Exchange Commission. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management's assumptions and estimates as of such date. We do not undertake any obligation to publicly update any forward-looking statements, whether as a result of the receipt of new information, the occurrence of future events or otherwise.
CONTACTSCompany Contact:Erik Holmlin, CEOBionano Genomics, Inc.+1 (858) 888-7610eholmlin@bionanogenomics.com
Investor Relations and Media Contact:Amy ConradJuniper Point+1 (858) 366-3243amy@juniper-point.com
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Bionano Genomics Announces ESHG Lineup Featuring 11 Customer Presentations of OGM Data Spanning Three Major Clinical Research Areas of Application...
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