Category Archives: Genetics

Live Animal Genetics Market Boosting the Growth Worldwide: Live Animal Genetics Market Dynamics and Trends, Efficiencies Forecast 2025 – Scientect

The report is an all-inclusive research study of the global Live Animal Genetics market taking into account the growth factors, recent trends, developments, opportunities, and competitive landscape. The market analysts and researchers have done extensive analysis of the global Live Animal Genetics market with the help of research methodologies such as PESTLE and Porters Five Forces analysis. They have provided accurate and reliable market data and useful recommendations with an aim to help the players gain an insight into the overall present and future market scenario. The Live Animal Genetics report comprises in-depth study of the potential segments including product type, application, and end user and their contribution to the overall market size.

The Live Animal Genetics Market carries out financial changes that occur year by years in market, with information about upcoming opportunities and risk to keeps you ahead of competitors. The report also describes top company profiles that present in market with trends worldwide. This research guided you for extending business.

The Live Animal Genetics Market research report presents a comprehensive assessment of the market and contains thoughtful insights, facts, historical data and statistically-supported and industry-validated market data and projections with a suitable set of assumptions and methodology. It provides analysis and information by categories such as market segments, regions, and product type and distribution channels.

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The key players covered in this studyGenus PLCHendrix GeneticsEW GroupZoetisCRV HoldingGrimaudTopigs NorsvinAlta GeneticsNeogen CorporationEnvigo

Market segment by Type, the product can be split intoAnimal Genetics ProductsAnimal Genetics Testing ServicesMarket segment by Application, split intoBovinePorcinePoultryCanineOther

Market segment by Regions/Countries, this report coversNorth AmericaEuropeChinaJapanSoutheast AsiaIndiaCentral & South America

The study objectives of this report are:To analyze global Live Animal Genetics status, future forecast, growth opportunity, key market and key players.To present the Live Animal Genetics development in North America, Europe, China, Japan, Southeast Asia, India and Central & South America.To strategically profile the key players and comprehensively analyze their development plan and strategies.To define, describe and forecast the market by type, market and key regions.

In this study, the years considered to estimate the market size of Live Animal Genetics are as follows:History Year: 2015-2019Base Year: 2019Estimated Year: 2020Forecast Year 2020 to 2026For the data information by region, company, type and application, 2019 is considered as the base year. Whenever data information was unavailable for the base year, the prior year has been considered.

A proper understanding of the Live Animal Genetics Market dynamics and their inter-relations helps in gauging the performance of the industry. The growth and revenue patterns can be revised and new strategic decisions taken by companies to avoid obstacles and roadblocks. It could also help in changing the patterns using which the market will generate revenues. The analysis includes an assessment of the production chain, supply chain, end user preferences, associated industries, proper availability of resources, and other indexes to help boost revenues.

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Market Segmentation based On Type, Application and Region:

The global Live Animal Genetics is analyzed for different segments to arrive at an insightful analysis. Such segmentation has been done based on type, application and Region.

Global Live Animal Genetics market is presented to the readers as a holistic snapshot of the competitive landscape within the given forecast period. It presents a comparative detailed analysis of the all regional and player segments, offering readers a better knowledge of where areas in which they can place their existing resources and gauging the priority of a particular region in order to boost their standing in the global market.

The Global Live Animal Genetics Market is gaining pace and businesses have started understanding the benefits of analytics in the present day highly dynamic business environment. The market has witnessed several important developments over the past few years, with mounting volumes of business data and the shift from traditional data analysis platforms to self-service business analytics being some of the most prominent ones.

For the future period, sound forecasts on market value and volume are offered for each type and application. In the same period, the report also provides a detailed analysis of market value and consumption for each region. These insights are helpful in devising strategies for the future and take necessary steps. New project investment feasibility analysis and SWOT analysis are offered along with insights on industry barriers. Research findings and conclusions are mentioned at the end.

Reasons for Buying This Report:

It Provides A Forward-Looking Perspective on Different Factors Driving or Restraining Market Growth.

It Provides A Five-Year Forecast Assessed on The Basis of How the Market Is Predicted to Grow

It Helps in Understanding the Key Product Segments and Their Future.

It Provides Pin Point Analysis of Changing Competition Dynamics and Keeps You Ahead of Competitors.

It Helps in Making Informed Business Decisions by Having Complete Insights of Market and By Making an In-Depth Analysis of Market Segments.

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Live Animal Genetics Market Boosting the Growth Worldwide: Live Animal Genetics Market Dynamics and Trends, Efficiencies Forecast 2025 - Scientect

Organigram Joins Medical Cannabis by Shoppers Inc. and TruTrace in Effort to Track Source and Genetics of Cannabis Used by Medical Patients – Business…

MONCTON, New Brunswick--(BUSINESS WIRE)--Organigram Holdings Inc. (NASDAQ: OGI) (TSX: OGI), the parent company of Organigram Inc. (the Company or Organigram), a leading licensed producer of cannabis, is pleased to announce it has partnered with Medical Cannabis by Shoppers(Shoppers) on Phase 2 of Shoppers Pilot Program powered by software partner TruTrace Technologies Inc. (CSE: TTT; OTCQB: TTTSF) (TruTrace).

The program is designed to genetically finger-print all participating cannabis products, tracking them throughout the supply chain, from genome to patient, in order to provide real-time information about the composition of each cannabis product used by Medical Cannabis by Shoppers customers.Organigram will provide cannabis products to Shoppers for use in the tracking program.

Standardized and validated testing of medical cannabis, ensuring consistent quality and efficacy, are critical to the products value as a viable treatment option. Likewise, product information such as strain composition and potency can help healthcare practitioners and patients make more informed and confident decisions about their medical cannabis treatment regimens.

Organigram is proud of our long-standing commitment to our medical cannabis community. From the development of innovative products to the support offered by our patient care team and programs, patients and their needs are at the heart of our medical cannabis business, says Greg Engel, CEO, Organigram. We also recognize how critical consistency is to patients and their healthcare providers so are pleased to partner with Shoppers, providing our products so that they can be followed from raw material to finished product, to offer them important, useable product insights.

Using Trutraces StrainSecure system, the program collects plant testing data and performs genomic verification in plant batches which are then registered in a blockchain-enabled database for intellectual property protection and strain validation. All information gathered from the plants, including their molecular and chemical makeup, can be tracked via the technology.

As jurisdictions around the world have begun to legalize and adopt cannabis as a medical treatment, there has been an influx ofnew breeders and growers and a profusion of new cannabis strains, each with a different representation of at least 500 known metabolites. Subtle changes in the chemical expression of various strains, whether by genetic structure or environmental conditions, may have significant clinical effects on the patients using this treatment option.With so many strains available, and with relatively limitedinformationon strain composition or genetic lineage and their relation to their chemical output, patients havelittleability to control what they aretaking over time.

In the absence of assigned drug identification numbers (DIN)for cannabis products, quantifying the genetics and metabolomics, as well as potency and equivalencies ofcannabis products is of interest to producers, distributors, shippers, government agencies, payers, clinicians and patients.

Maintaining an effective traceability ecosystem about these details throughout the supply chain is a component of providing consistent medicine, says Engel.

Using TruTrace technology, Shoppers has partnered with University Health Network in Toronto (UHN) to launch Medical Cannabis Real World Evidence (MCRWE), a new ground-breaking study on cannabis and health which will track outcomes with TruTrace validated product for the first time in history.

This novel observational study is targeting a minimum of 2,000 patients who will be followed over a 24-week period. Enrolled patients will have access to certain fully verified products on the Medical Cannabis by Shoppers platform, which have been tested for detailed cannabinoid and terpene profiles.More information about the study can be found here.

About Organigram Holdings Inc.

Organigram Holdings Inc. is a NASDAQ Global Select and TSX listed company whose wholly owned subsidiary, Organigram Inc., is a licensed producer of cannabis and cannabis-derived products in Canada.

Organigram is focused on producing high-quality, indoor-grown cannabis for patients and adult recreational consumers in Canada, as well as developing international business partnerships to extend the Company's global footprint. Organigram has also developed a portfolio of legal adult use recreational cannabis brands including The Edison Cannabis Company, AnkrOrganics and Trailblazer. Organigram's facilityis located inMoncton, New Brunswick and the Company is regulated by theCannabis Act and theCannabis Regulations(Canada).

This news release contains forward-looking information. Often, but not always, forward-looking information can be identified by the use of words such as plans, expects, estimates, intends, anticipates, believes or variations of such words and phrases or state that certain actions, events, or results may, could, would, might or will be taken, occur or be achieved. Forward-looking information involves known and unknown risks, uncertainties and other factors that may cause actual results, events, performance or achievements of Organigram to differ materially from current expectations or future results, performance or achievements expressed or implied by the forward-looking information contained in this news release. Risks, uncertainties and other factors involved with forward-looking information could cause actual events, results, performance, prospects and opportunities to differ materially from those expressed or implied by such forward-looking information include factors that change supply quantities; risks associated with international jurisdictions including regulatory risk; receipt of any required permits from Health Canada and other authorities; including general risks related to COVID-19 and risks as disclosed in the Companys most recent annual information form, managements discussion and analysis and other Company documents filed from time to time on SEDAR (see http://www.sedar.com) and filed or furnished to the Securities and Exchange Commission on EDGAR (see http://www.sec.gov). Readers are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. Although the Company believes that the assumptions and factors used in preparing the forward-looking information in this news release are reasonable, undue reliance should not be placed on such information and no assurance can be given that such events will occur in the disclosed time frames or at all. The forward-looking information included in this news release are made as of the date of this news release and the Company disclaims any intention or obligation, except to the extent required by law, to update or revise any forward-looking information, whether as a result of new information, future events or otherwise.

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Organigram Joins Medical Cannabis by Shoppers Inc. and TruTrace in Effort to Track Source and Genetics of Cannabis Used by Medical Patients - Business...

Iowa research team wins grant to study growth, genetics and nutrition in pigs – The Pig Site

A research group led by Jack Dekkers, Distinguished Professor in the Department of Animal Science at Iowa State University, has received a grant from the National Institute of Food and Agriculture to further genetic improvement of livestock by integrating biological models of growth that have been developed by animal nutritionists.

The $500,000, two-year grant for Dekkers and his team will support the project, Integration of Biological Models in Genomic Evaluation: Pig-Growth-Model Whole Genome Prediction (PGM-WGP),as part of a national USDA initiative for Research in Tools and Resources for Animal Breeding, Genetics and Genomics Research.

Genomic evaluation and selection are used to improve the rate of genetic gain by identifying the animals with the best genetics for traits of economic importance. Using these animals for breeding future generations results in a more profitable final product, increased value of by-products and more. However, existing genomic evaluation models often fail to predict how the progeny of an animal will perform when they are exposed to diverse environmental conditions.

This research will take an existing genomic model and integrate it with models of growth that have been developed and used to formulate diets for pigs. This will allow breeders to better predict the genetics of an animal that underpin an animals ability to grow under different environmental conditions, including temperature, humidity, diets and disease.

"The idea to incorporate a biological growth model into genomic evaluation of pigs is based on similar work that has been conducted by scientists at Corteva, formerly Pioneer, who have successfully integrated crop-growth models into genomic evaluation to predict the performance of corn hybrids under normal versus drought conditions," said Dekkers.

Co-director Nick Sero, assistant professor of animal breeding, agreed, The integration of biological models with genomic models is expected to have a significant impact on genetic improvement for different environments in the swine industry.

To develop the model, the team will use in-depth data on feed intake, body weights and body composition on pigs from several lines from a commercial breeding company. The resulting model will be validated using this data to demonstrate its ability to improve prediction.

This project is being directed by Dekkers and will be co-directed by Sero and Andrea Doeschl-Wilson, reader and group leader of the Mathematical Modeling Group and Deputy Head of Genetics and Genomics Division of the Roslin Institute in Edinburgh.

Other team members include Iowa State faculty Rohan Fernando, professor of animal breeding, Jayasooriya Ranga Appuhamy, assistant professor of animal nutrition, along with a post-doctoral fellow and a PhD student who will be appointed to help conduct the research. Another collaborator is Jaap van Milgen, senior researcher and deputy-head of the INRAe-Agrocampus West Research Unit and developer of the INRA-Porc growth nutrition model. Several industry partners are also involved to supply insight, provide access to data and help facilitate model validation.

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Iowa research team wins grant to study growth, genetics and nutrition in pigs - The Pig Site

First-Ever Consumer DNA Test to Unlock the Connection Between Genetics and Mental Wellness-Related Behavioral Tendencies – PR Web

NEW YORK (PRWEB) August 19, 2020

Living with a mental health challenges can be stressful even during the best of times. Then COVID-19 came along. Quarantine, distancing, not seeing family and loved ones, and economic worries have all added to the struggles of people dealing with mental wellness. On top of that, back-to-school stress is compounding the mental stressors were all dealing with right now. Recently, Amy Edgar, Founder of Childrens Integrated Center for Success and expert in pediatric mental health, teamed with YourUpdateTV to discuss steps we can take to take control of our mental wellness during this uncertain time.

A video accompanying this announcement is available at: https://youtu.be/0WpBE2FWYC0

Parents, many of whom may be dealing with their own mental and emotional struggles, have taken on the burden of worrying about their childs mental health as well. With the back to school season in full swing, stress and anxiety are at an all-time high as families grapple with the reality of additional distance learning, or the potential dangers of returning to the classroom. Its natural for parents to wonder whether the last five months and whatever lies ahead will have a lasting effect on kids mental well-being.

So how can parents take back control of mental wellness in the age of COVID-19?

A first-ever consumer DNA test is helping unlock the connection between genetics and mental wellness. One cheek swab will produce results that will help people better understand how genes affect ones predisposition for stress, focus, substance abuse, sleep, and more.

Organized around Genominds proprietary 7 Core Genetic Mental Health Capabilities, the test analyzes 38 genetic variants and their influence on 29 mental health traits. The result is an interactive report that details 59 possible behavioral predispositions specific to each users genetic profile, along with resources and actionable recommendations shown to improve wellness and quality of life. Genomind Mental Health Map is the only DNA test in the consumer market with a specific focus on mental health and wellness, and is available without prescription. The test should not be used as a diagnostic or risk assessment for mental health diseases and disorders.

For more information, visit MentalHealthMap.com and use discount code MHMFALL5.

About Amy Edgar, APRN, CRNP, FNP-C:Amy Edgar is transforming healthcare and embracing our next generation of humans. Ignited by the experience of raising her now 19-year old daughter, Amy founded the Children's Integrated Center for Success in 2014. Weaving together the threads of mom, entrepreneur, teacher, nurse, primary care provider, and science geek, Amy utilizes systems thinking and integrated care delivery models to run her primary care center focused on children with behavioral health needs. From cutting edge genetics research to nutrition consults, speech and equine therapy, school advocates, and marriage counselors CICS strives to reach every child, every time. In 2017, Amy led CICS in connecting career opportunities for children with autism looking for suitable work to capture their own piece of the American Dream, which was realized in the CICS Foundation. Amy continues to practice and provide patient care while championing CICS's virtual healthcare expansion to reach families across and outside of Pennsylvania.

About Genomind:Genomind is a leading mental health company singularly focused on filling the innovation gap in mental health care through novel, genetics-based tools that bring mental health into the era of personalized medicine. Its flagship product, Genomind Professional PGx, is a pharmacogenetic testing service that helps medical professionals guide patients mental health treatment. The Company recently launched Genomind Mental Health Map a direct-to-consumer test that enables a better understanding of the biological basis of mental health, coupled with actionable guidance to help people improve health and wellness. Supported by a world-class genetics lab, a unique heritage of clinical mental health expertise, and a consultative approach, Genomind is advancing a new paradigm of precision medicine in mental health care. Learn more at http://www.genomind.com.

About YourUpdateTV: YourUpdateTV is a social media video portal for organizations to share their content.

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First-Ever Consumer DNA Test to Unlock the Connection Between Genetics and Mental Wellness-Related Behavioral Tendencies - PR Web

Seed Genetics Direct Field Days will be held as scheduled – Ohio’s Country Journal and Ohio Ag Net

As fall approaches, Seed Genetics Direct will host its annual field days in Ohio and Indiana between August 25 and Sept. 16 (see schedule below). Seed Genetics Direct is an independent seed company headquartered in Jeffersonville, Ohio that serves the Eastern Corn Belt.

Free and open to the all farmers, field days provide the opportunity for visitors to tour corn and soybean plots to see the performance of 2021 genetics and technologies. Seedsmen will also be available to provide detailed information and answer questions.

Weve added seven new corn hybrids and nine soybean varieties to our lineup for the Eastern Corn Belt. Field days are great opportunity to see products, as well stock up on the best deals of the season. Our September discounts include a 15.5% early-pay discount or a 9.5% savings with John Deere zero percent financing, as well as $10 off per unit of traited corn, said Todd Jeffries, SGD vice president. In addition, we offer explosive treatments at a standard price on corn, soybeans and wheat. These treatments protect from Barley Yellow Dwarf, Fusarium, Pythium, Phytophthora, Phomopsis, Rhizoctonia and more! Our corn treatment also includes N-Hibit and Terios Zn+ for vigor and stress tolerance. Guests can learn more about these offerings during our field days.

Seed Genetics also has several practices in place to protect guests from the spread of COVID-19 during field days. To disperse crowds, SGD field days will occur all day between 11 a.m. and 7 p.m. to ensure plot tours are in groups of 10 or less; guests may arrive at any time. Freshly grilled and individually-packaged food will also be served throughout the day by servers in masks and gloves. SGD will provide guests with disposable masks, gloves and hand-sanitizer as needed, as well as follow all Ohio, Indiana, CDC and OSHA mandates.

Seed Genetics Direct field days will occur as scheduled below. To ensure events have not been cancelled, on the day of the event, please call the SGD main office at 740-505-6545 or check SGDs website (seedgeneticsdirect.com), Facebook or Twitter channels (@seedgenetics).

SGD field days scheduleAll SGD field days are from 11 a.m.- 7 p.m. Guest can arrive at any time.

August 25: Chillicothe, Ohio plot on Schooley Station Road (east of Chillicothe on Route 50, south onLancaster Road, east on Schooley Station) (Bob, Brian, and BJ Brown)

August 26: 2741 Weigand Road, Lockbourne, Ohio 43173 (Bill, Bob and Ross Black)

August 31 and Sept. 1: 4712 Prairie Road Northeast, Washington Court House, Ohio 43160

Sept. 4: 7263 North US Hwy 35, Williamsburg, Ind. 47393

Sept. 8: 8608 North Zaring Road, Scottsburg, Ind. 47170 (Wischmeier Farms)

Sept. 11: 8584 State Route 725 West, Camden, Ohio 45311 (Don Jackson)

Sept. 16: 4614 East State Road 244, Shelbyville, Ind. 46176 (Matt Settles)

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Seed Genetics Direct Field Days will be held as scheduled - Ohio's Country Journal and Ohio Ag Net

Genetic Study Reveals New Insights On Transatlantic Trade Of Enslaved People – Here And Now

Editor's note:This segment includes mentions of sexual violence.

Until recently, much of the information available about where enslaved people were captured before being brought to the Americas came from shipping logs and databases.

These sources detailed ports of embarkation and numbers of people transported, and new data drawn from genetics corroborates much of what historians already knew.

But the data also reveals some revelations both about the intercolonial trade of enslaved people and some of slavery's most brutal atrocities.

The study, which appears in the American Journal of Human Genetics, drew on genetic data from 50,000 23andMe users who agreed to lend their DNA.

The project was started by Joanna Mountain, a geneticist at 23andMe and former Peace Corps volunteer in Kenya who developed a deep interest in what happened to people who were wrenched from that continent into slavery. Mountain joined forces with population geneticist Steven Micheletti on the study that has been years in the making.

The pair worked closely with historians to compare a database of transatlantic slavery records to the genetic connections between people in Africa and people in the U.S. with African ancestry.

They found that there was a very strong bias toward African women contributing to the present-day gene pool compared to African men, and that the bias varies across different regions of the Americas, Mountain says.

In parts of Central America, enslaved African women were contributing 13 to 17 times more to the current day gene pool than enslaved African men, she says.

In discussing this extreme finding with historians and looking through the historical literature, we found indications that men were far less likely to reproduce, partly because they were at higher risk of dying early if they were having to participate in rice farming or sugar cane farming, which was very risky, she explains.

At the same time, enslaved African women were often being forced to reproduce. In parts of Latin America, there would be initiatives to encourage European men to father children with African women in order to do something that they called dilute the African gene pool, she says.

The rape of enslaved African women who were sometimes forced to have children before arriving in the U.S. as a strategy to manipulate the gene pool made their genes more extreme in certain areas.

This is something that we often think of as the past. And yet the repercussions certainly continue to today in the DNA, she says. It's kind of amazing that we see it so strongly in the genetic evidence.

On the over-represented number of Americans with Nigerian ancestry, which the study found is likely due to the intra-continental slave trade

Stephen Micheletti: We see a lot of U.S.-based African Americans with ancestry from Nigeria and specifically connections to the ethnolinguistic groups, the Yoruba, Esan and Igbo. And why this was so surprising is the transatlantic shipping records indicate that people around Nigeria weren't directly arriving in the U.S. in high numbers. But what we have to realize is that enslaved people were being forced between and within the Americas over centuries. So not all the movement was happening across the Atlantic. It was also happening between all these countries and within all of these countries.

On how few Gambian and Senegalese descendants of enslaved people there are in the U.S.

Micheletti: We merge these two regions and call them Senegambia. And we didn't see a lot of Senegambian representation in the U.S. and again, that's another deviance from our expectation given the shipping records. The working hypothesis is Senegambians were typically Asian and African rice cultivators back in Africa and the Europeans were well aware of this. So it's likely that Senegambians that arrived in the United States ended up on rice plantations because of their expertise. And what we know about rice plantations is that they were some of the most dangerous working conditions for enslaved people. One reason is malaria is a huge problem in these swampy rice fields, and there's also other risks like drowning

On the response from 23andMe volunteers

Joanna Mountain: We definitely got at quite a bit of response. And it's provoked some debate regarding enslavement and forced migrations. But also people seeing this story in their own lives. One individual said that whenever I'm in Jamaica and New Orleans, I feel a sense of connection. And for that individual, this study felt very real to him. And so that was super exciting for us.

On people discovering the study and making connections between European DNA and their ancestry

Micheletti: One goal of this study was first to produce the data and then look at the historical records that best support those data. And unfortunately, the records that support those data are these horrible atrocities. And with that, we wanted to make readers aware of these atrocities because they've shaped the genetic landscape across the Americas. And we want people to be aware of the number of enslaved people that were impacted.

... I would say [peoples] eyes are opened by this study because a lot of people may have not heard about this history in the past. And I've received some personal messages that people are happy that we're looking into the history and not just providing a genetic study, but more of a collaborative study with historians and not ignoring all of these atrocities because it's part of their past. People have discovered using services like ours that they have European ancestry and now they have better context for why that is.

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Genetic Study Reveals New Insights On Transatlantic Trade Of Enslaved People - Here And Now

New Generation Genetics Bulls Lead the Way Following the Genetic Evaluations in August – Hoard’s Dairyman

The information below has been supplied by dairy marketers and other industry organizations. It has not been edited, verified or endorsed by Hoards Dairyman.

Following the release of the August 2020 genetic evaluations, bulls from New Generation Genetics proven and genomic bulls ranked at or near the top for Milk, Components, Type, Udder Composite, Mobility, Fertility, DPR, Productive Life, NM$, PPR, & Profit.

54BS557 BMG Lust GET LUCKY *TM continues to lead the way as the #1 proven bull for milk, fat, and protein. Get lucky is also the #1 Proven bull for PPR at 189. His milk is +2594, +58f and +57p.

54BS558 Hilltop Acres B DAREDEVIL ET *TM is the breeds type leader with daughters impressing on farms and in the show ring. He continues as the #1 proven type bull at +1.0 with an udder composite now at +1.16.

54BS564 Jo-Lane Dario HAMPTON ET *TM dominates in health traits, profit, and fertility. After completing his 1st crop he ranks #4 for productive life at +5.2 with a +1.7 DPR. He is the new #5 proven Net Merit bull at $327 and #5 SCR ranking at +1.5.

54BS561 Hilltop Acres BV JESSE ET *TM is a new graduate at +624 milk, +0.6 type, +0.71 UDC, +0.7 DPR, and positive SCR. He offers an impressive outcross pedigree, phenomenal udders, and great dairy strength.

54BS601 La Rainbow Sweet SALSA ETV *TM Is the #1 G-type bull at +1.1 type and +1425 milk. This Genomic Gem is a LUCKY CARL brother to SILVER, giving him an impressive pedigree to back his historic numbers.

54BS604 La Rainbow Sweet SPARK *NP is a new genomic polled bull at +750 milk, +0.8 type, and +1.18 UDC, earning him #1 genomic polled status in these three categories.

196BS55878 Portmann BS Bays JONMAR *TM is an exciting new offering from Swissgenetics. He is the #8 G-PPR bull at 182 and #5 genomic Net Merit bull at $466. He is also +1158 milk, +43 fat, +40 protein, +0.79 UDC, and +2.1 DPR.

We also offer the CHAMPIONS COLLECTION elite sire lineup including 54BS600 WINRITE, 54BS602 FIRST CHOICE, 54BS539 RICHARD, 54BS581 RASTA, 54BS568 FAST & FURIOUS, and 54BS548 WINNING FORMULA.

New Generation Genetics offers the most comprehensive Brown Swiss Sires portfolio in the U.S. For further information call 920-568-0554, visit our Facebook page http://www.facebook.com/newgenerationgenetics, email info@brownswiss.com or visit http://www.brownswiss.com.

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New Generation Genetics Bulls Lead the Way Following the Genetic Evaluations in August - Hoard's Dairyman

How extremely rare genetic condition leaves 11-year-old Amelia needing a wheelchair at any moment – Yorkshire Post

LifestyleFamilyAmelia Beaton suffers from a rare genetic condition which means she can be fine one minute and need a wheelchair the next. Catherine Scott reports.

Wednesday, 19th August 2020, 4:45 pm

Eleven-year-old Amelia Beaton suffers from a rare genetic condition which affects just 40 people in the UK.

Eating and drinking is a real difficulty for Amelia, says mum Lisa. Amelia is in a lot of pain and has lots of gastrointestinal problems.

Its known as Little Britain syndrome, as in the TV show. Its like the Andy character. One minute she can be running around, at her own pace, then she is exhausted and in pain.

It doesnt affect Amelias learning ability and its hard as she knows exactly what is going on. More often than not however, Amelia is feisty, cheeky and desperate to get on with things. She is very creative and likes to draw on her iPad. She bounces on her trampoline and loves to sing. She wants to be a singer or an actress. She is popular at school and we keep everything positive. But she has had so much time in hospital.

Amelia, who lives in Knaresborough is the youngest child of Lisa, 45, and husband Martin, 52, an airline pilot. Their older children are Harry, 20, Jack, 17, and George, 13.

During her pregnancy with Amelia, Lisa had excessive amniotic fluid which can be an indicator of a health problem and reduced foetal movements. Nonetheless,

Amelia passed all her newborn health checks. But by the time she was two weeks old, Lisa had started to worry, firstly at her babys high-pitched cry, then struggles breastfeeding and her stiff body position.

I knew something was not right, Lisa recalls. I asked my health visitor and she said after three boys I was letting my girl rule the roost. Around a week later I pointed out again that she was holding her head in a weird position. The health visitor thought it could be a neck problem caused by the position she was in during pregnancy. My GP started a referral to orthopaedics.

Shortly after Lisa was undressing Amelia for a baby clinic check when a different health visitor asked if she could take her to see the GP on duty.

The GP examined Amelia but didnt give anything away. She just said she had some concerns and wanted paediatricians at the local hospital in Jersey, where we were living at the time, to see her urgently. She asked me to go straight there and not go home.

At hospital, doctors took a full medical history and even asked if Martin and I were blood relations. Amelia was then taken for tests and an X-ray. I felt like I had been smacked in the face. As far as I knew we were just waiting for a referral for a neck issue. I remember when the doctors came back to us, I was so scared.

The paediatrician suspected arthrogryposis, a stiffening of joints and muscles. He said we would need to see a specialist in London. He told me there is a form of the condition where children dont live past the age of two and recommended us not to Google it. I did Google because it was impossible not to. I wanted to know as much as I could, to understand, learn and prepare as best I could. I also felt that having already been told there was a form where children dont live long, that was already the worst possible news as far as we were concerned so I wanted to read positive stories, outcomes and experiences.

It was hard seeing images of older children with the condition but like all things, there is a wide. We went home and had a three-week wait before we went to London.

Amelia saw a private orthopaedic consultant at the Portland Hospital in London and started a programme of extensive physiotherapy three times a day as well as therapy three times a week at the Childrens Development Centre.

She was referred to Great Ormond Street Hospital for tests and MRI scans. Amelia was seen by a neurologist, geneticist, physiotherapist, respiratory consultant and dietitian. A muscle test in June 2009 test showed Amelia most likely had congenital myasthenic syndrome.

Congenital myasthenic syndrome (CMS) is a neuromuscular genetic disorder characterised by muscle weakness that worsens with physical exertion. Affected children may experience mobility issues, owing to weakness in the skeletal muscles; problems eating, owing to weakness in the muscles used for chewing and swallowing; and problems controlling facial movement, owing to weakness in the facial muscles and muscles controlling the eyes and eyelids.

Amelia is believed to possibly have an extremely rare variation. In the UK, 40 families are affected by this genetic disorder. CMS is most commonly caused by autosomal recessive inheritance. This means that it has been inherited because both parents carry one faulty gene copy. Less commonly, CMS is passed on by one parent.

I was nave back then. For the first year I thought every time we went back to GOSH we would be told what was wrong with her. No one told us it would be such a long round with genetics so we were unprepared for how long everything took or that we would get negative results or just no fault found. We were back and forth to GOSH over the next few years.

Amelia is now 11 years old. She has muscle weakness, fatigue and difficulty swallowing and eating. She has one-to-one help at school. She needs help with day to day activities such as personal care and cutting up her food. Her upper limbs are very tight, but her lower limbs are hypermobile. She can walk, but tires quickly so when she does, she uses her wheelchair.

Last year we were in hospital for three months. It is hard on all of us. I would love to get a firm diagnosis. It is unlikely to be of use to Amelias treatment, but it would make a big difference to me as parents you want to know you have done the best for your child.

Charitys support for family

The family has been supported by the charity MyAware, which funds residential family weekends.

The weekend provides the opportunity for families to mix, support each other and provides information that is vitally needed with such a rare condition. MyAware us supported by the Jeans for Genes campaign.

Jeans for Genes Day raises money for Genetic Disorders UK, the charity that aims to change the world for children with genetic disorders. Funds raised will go to the vital care and support they need.

Jeans for Genes Day takes place Monday-Sunday September 14 to 20 and invites everyone to wear their jeans to work or school and make a donation. http://www.jeansforgenesday.org.

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How extremely rare genetic condition leaves 11-year-old Amelia needing a wheelchair at any moment - Yorkshire Post

A genetic map hopes to trace rescued chimps back to their homes – Mongabay.com

Experts estimate that nearly 2,000 chimpanzees may be lost to the wildlife trade each year. Once taken from the wild, young chimpanzees that survive the trauma of capture are sold as pets or for entertainment and can end up almost anywhere; theyve been intercepted by authorities in locations all over the globe.

Theyre confiscated in maybe Moscow, or San Francisco, or Hong Kong it can be anywhere and we dont know where they came from, says Peter Frandsen, a conservation genomics researcher at Copenhagen Zoo in Denmark.

Thats a problem when conservationists need to decide which countrys sanctuaries an animal should return to or where it could be safely reintroduced into the wild.

The answer may lie in the chimpanzees own genetic code. A global team of researchers is working to determine how chimpanzee genetics vary based on where the animals come from. By creating this genetic reference map, scientists hope to be able to determine the origins of confiscated chimpanzees as well as identify high-risk areas for wildlife trafficking.

Just a century ago, a million chimpanzees roamed the rainforests and grasslands of Africa. Now, fewer than 200,000 may be left in the wild, and conservationists fear that without widespread change these animals may go extinct in their natural habitats.

Pretty much all of the big conservation threats are facing chimpanzees right now, says Mimi Arandjelovic, a primatologist at the Max Planck Institute for Evolutionary Anthropology in Germany. Logging, mining, all of the extractive industries that are going on in equatorial Africa And then of course theres the huge threat of disease Theres the bushmeat trade, so people hunt and eat apes. And theres the primate pet trade.

Chimpanzees are currently listed as endangered by the IUCN (the western chimpanzee, one of four subspecies, is listed as critically endangered), and their numbers are still declining.

While chimpanzee conservation has many components, researchers say genetic studies are an increasingly important piece of the conservation puzzle.

One recently published study sheds new light on just how valuable genetic information could be in the conservation of this endangered species.

In this study, a group of researchers from Denmark, Spain, Russia and the U.K. analyzed nearly 60,000 ancestry-related genetic markers from captive-born and wild-born chimpanzees. In collaboration with dozens of zoos and sanctuaries across Europe and Africa, the researchers used hair samples to source DNA, a technique that is less invasive and stressful for animals than collecting blood.

Using the genetic data from wild-born chimpanzees whose birthplace was known, the researchers constructed a genetic reference map. They then compared this map with the DNA from chimpanzees who ended up in sanctuaries after being confiscated from illegal wildlife trafficking operations. In this way, researchers were able to estimate where the sanctuary chimpanzees had come from.

So just like popular DNA testing services for humans can tell us about our ancestry and origins, genetic information can reveal where chimpanzees come from.

Frandsen, one of the study authors, says learning where chimpanzees come from is important for many reasons.

For example, he says, genetic analysis provides essential information for captive-breeding programs. Even though chimpanzees may all look similar, there are actually four different accepted subspecies (and a fifth proposed subspecies), each with their own distinct range and unique genetic makeup. But there arent always records about where animals come from and which subspecies they are, which makes it difficult for captive-breeding programs to maintain the integrity of subspecies.

Frandsen says its important for captive-breeding programs to preserve these unique subspecies. Modern zoos are often referred to as Noahs Arks. You could call it a living museum sample, he says. So, we want to make sure that [zoo populations] resemble what you would find in the wild.

That way, he says, if a subspecies goes extinct in the wild, it wouldnt be lost altogether and eventually individuals of that subspecies could be reintroduced to the wild from these captive populations.

But genetic information may be even more valuable for combating animal trafficking.

Arandjelovic, who was not involved in the 2020 study by Frandsen and colleagues, says its unfortunately common for people to kill chimpanzee mothers for bushmeat and sell the babies as pets. Chimpanzees that are recovered from this wildlife trade can be candidates for reintroduction into the wild, so knowing where they came from is essential for deciding where they should be released.

Although Frandsen acknowledges that reintroduction can be challenging, especially as animals get older, he says its still very important. Theyre filling up in the sanctuaries, they dont have enough space and one of the main goals is to reintroduce as many as they can, he says. The sanctuary shouldnt be the endpoint for these chimpanzees if theres an opportunity to relocate them. Determining where an animal came from using genetic data may give it a better chance at a successful return to the wild.

Its possible that genetic data could even help prevent chimpanzee trafficking altogether. Identifying where chimpanzees in the illegal pet trade have come from could reveal poaching hotspots, thus allowing countries to appropriately target anti-poaching efforts. This is especially important in places where conservation funding may be limited.

But Frandsen says they dont yet have enough data to identify these high-risk areas. In this early proof-of-principle project, researchers analyzed just a few dozen animals that were rescued from the wildlife trade and ended up in sanctuaries. Frandsen says there are about 1,000 chimpanzees currently in African sanctuaries; the research team wants to expand their data collection to include these animals so that they can build a more accurate picture of poaching hotspots.

Future projects also include collecting more data from individuals born at known locations to build a more detailed genetic reference map, Frandsen says. The more detailed this map is, the more accurately researchers can determine where a trafficked animal has been taken from.

For some of the subspecies, we have pretty good data from the wild, Frandsen says. But for some of the other subspecies we are still data-deficient. So right now, the plan is to fill those knowledge gaps on the map.

Arandjelovic agrees that having accurate and detailed genetic reference maps is very important for determining the provenance of apes confiscated from the pet trade. She says the technique used in the present study analyzing thousands of different markers provides very detailed information about an individual. However, because of the cost and the specialized supplies needed to run this sort of analysis, it often cannot be done in the chimpanzees country of origin.

She says she wants to see if a reference map could be built using a simpler and cheaper technique that analyzes fewer locations in the genome. This technique would have the advantage of being more feasible to carry out in the countries where chimpanzees live. It would be great if we didnt have to export the samples, if we could do everything in-country, she says. That would be faster (we dont have to deal with permits), but we can also start capacity-building and having people in the country of origin do that work instead of sending it to Europe or North America. On the other hand, its not yet clear if this simpler technique would provide enough genetic information to create a useful reference map.

Frandsen and Arandjelovic agree that this is just the beginning for the application of genetic techniques to locate the origins of trafficked animals. The present study is a proof of concept, Frandsen says. So, theres a lot of work ahead to complete this project, but this is just for the chimpanzees, he says. Its also really a blueprint for other conservation projects. There are a ton of other taxa that this could be applied to.

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A genetic map hopes to trace rescued chimps back to their homes - Mongabay.com

Consistent associations between human genetic variation and the gut microbiome identified in 3 independent European cohorts – Gut Microbiota for…

Many thousands of studies about gut microbiota and 16s RNA analysis are available to us nowadays. And while many results and interesting concepts emerge from those studies, a gold standard protocol for data analysis is not yet available. Moreover, the studies are carried out by different teams from different parts of the world, their designs are not the same, DNA extraction protocols differ, and 16s RNA region sequences vary between projects. As such, sample processing variables and the numerous environmental factors influencing an individuals gut microbiota mean association studies between the human genome and gut microbiota genome are less powerful.

Writing in Nature Microbiology, David A. Hughes and colleagues have created a new analytical pipeline that disentangles associations between human host genotype and gut microbiome variation in 3 distinct cohorts, paving the way for causal inference analyses in the field.

Researchers harmonized the analytical pipeline across three independent cohorts: the Flemish Gut Flora Project (n = 2,223) and two German cohorts (Food-Chain Plus, n=950; and PopGen, n= 717).

Using fecal 16s RNA gene sequencing, the researchers first estimated the proportion of gut microbiome variation explained by genetic variation (heritability) between individuals. In total, they identified 13 genera that were heritable. Eight were from the phylum Firmicutes, five of which were from the family Lachnospiraceae and two from Ruminococcaceae.

Dorea and Anaerostipes genera, which are short-chain fatty acid producers, along with Hespellia were three of the most heritable bacteria.

During a second stage, the researchers identified associations between bacteria species and human genes, encountering two strong associations:

The two strong associations were followed by the discovery of 11 associations showing low heterogeneity. Among those 11 associations, they found a relationship between the butyrate-producing genus Butyricicoccus and the SLC5A11 gene, which is a sodium-dependent myo-inositol glucose cotransporter that is highly expressed in the brain and intestine. The findings are in agreement with previous studies suggesting that butyrate-producing bacteria are associated with blood glucose and appetite regulation.

Another association was identified between Veillonella and rs117338748. This gene is involved in regulating low-density lipoproteins (LDLs) and transporting high-density lipoproteins (HDLs). The researchers observed that the presence of Veillonella was associated with a drop in LDL-cholesterol.

Using a Mendelian randomization model, the researchers estimated relationships between 5 microbial pathways and 7 outcomes (diseases). For instance, Bifidobacterium was associated with body composition. However, in the absence of clear microbiome-driven effects, any interpretation requires caution. In other words, it could be the causeless Bifidobacterium means the individual has a higher body mass index (BMI)or the consequencean individual with a higher BMI will present less Bifidobacterium in their gut.

In conclusion, this in-depth study on human genome-gut microbiome associations in 3 distinct cohorts generated a growing catalogue of genetic associations and showed better associations between the hosts genetics and its gut microbiota. Next steps should look at understanding the causation factors for a better understanding of gut microbiota function and association with outcomes.

Reference:

Hughes DA, Bacigalupe R, Wang J, et al. Genome-wide associations of human gut microbiome variation and implications for causal inference analyses. Nat Microbiol. 2020. doi: 10.1038/s41564-020-0743-8.

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Consistent associations between human genetic variation and the gut microbiome identified in 3 independent European cohorts - Gut Microbiota for...