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Janos Haits

UCSC Genomics Text Indexing - 0 views

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    UCSC Genome Bioinformatics Genocoding Project Genomic Text Indexing: Scanning papers for genomic identifiers and mapping them to the human genome. We currently recognize DNA and protein sequences, SNPs, bands and gene symbols.
Janos Haits

api.23andme.com/ - 0 views

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    The Personal Genome API. Build an app on the human genome
Erich Feldmeier

Der Mann, der das Genom salonfähig machte: Frank Schirrmacher (Archiv) - 0 views

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    " 27.06.2000, FAZ #Schirrmacher Biologie.- Vor zehn Jahren, als das Genom weltweit gefeiert wurde, berichteten alle Zeitungen der Welt über dieses Ereignis. In Deutschland überraschte damals die "FAZ" mit einer ungewöhnlichen Idee: Sie brachte den biologischen Code ins Blatt: viele Seiten Buchstabengewirr aus A,T,G und C. Wer den Mitherausgeber und Feuilleton-Chef der "Frankfurter Allgemeinen Zeitung", Frank Schirrmacher, besuchen möchte, muss vorbei am Code des Lebens. Schon auf dem Flur: Eingerahmte Zeitungsseiten mit den vier Buchstaben A, T, G und C, vieltausendfach. Die Ausgabe stammt vom 27. Juni 2000, dem Tag als die Nachricht von der Entzifferung des menschlichen Genoms um die Welt ging. "
Charles Daney

What we're learning about pancreatic cancer now - and why the cure remains so elusive >... - 0 views

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    Genomes aren't orderly and neat; they're exceedingly messy and complex, filled with "noise" from which subtle signals are difficult to filter. A disease can arise from one or two mutations, or from the cumulative action of hundreds. This means finding genome mutations responsible for diseases is both incredibly difficult and also often fruitless: The variation in individual genomes is so large that nearly every single potential disease-causing mutation typically turns out to be benign.
Skeptical Debunker

The genetic footprint of natural selection - 0 views

  • During evolution, living species have adapted to environmental constraints according to the mechanism of natural selection; when a mutation that aids the survival (and reproduction) of an individual appears in the genome, it then spreads throughout the rest of the species until, after several hundreds or even thousands of generations, it is carried by all individuals. But does this selection, which occurs on a specific gene in the genome of a species, also occur on the same gene in neighboring species? On which set of genes has natural selection acted specifically in each species? Researchers in the Dynamique et Organisation des Génomes team at the Institut de Biologie of the Ecole Normale Supérieure (CNRS/ENS/INSERM) have studied the genome of humans and three other primate species (chimpanzee, orangutan and macaque) using bioinformatics tools. Their work consisted in comparing the entire genomes of each species in order to identify the genes having undergone selection during the past 200,000 years. The result was that a few hundred genes have recently undergone selection in each of these species. These include around 100 genes detected in man that are shared by two or three other species, which is twice as many as might be anticipated as a random phenomenon. Thus a not inconsiderable proportion of the genes involved in human adaptation are also present in the chimpanzee, orangutan or macaque, and sometimes in several species at the same time. Natural selection acts not only by distancing different species from each other when new traits appear. But by acting on the same gene, it can also give rise to the same trait in species that have already diverged, but still have a relatively similar genome. This study thus provides a clearer understanding of the group of genes that are specifically implicated in human evolution (during the past 200,000 years), as it allows the identification of those genes which did not undergo selection in another primate line. An example that has been confirmed by this study is the well-known case of the lactase gene that can metabolize lactose during adulthood (a clear advantage with the development of agriculture and animal husbandry). The researchers have also identified a group of genes involved in some neurological functions and in the development of muscles and skeleton.
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    A further step has been taken towards our understanding of natural selection. CNRS scientists working at the Institut de Biologie of the Ecole Normale Supérieure (CNRS/ENS/INSERM) have shown that humans, and some of their primate cousins, have a common genetic footprint, i.e. a set of genes which natural selection has often tended to act upon during the past 200,000 years. This study has also been able to isolate a group of genes that distinguish us from our cousins the great apes. Its findings are published in PloS Genetics (26 February 2010 issue).
Nits Mahajan

Take Advantage Of Clinical Genomics Market - Read This Research Report By World Researc... - 0 views

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    Clinical Genomics Market By Test Type (Diagnostic, Genetic, Newborn Screening, Prenatal, Carrier Screening), Software, Method (Molecular, Chromosomal, Biochemical Tests), End User (Hospitals and Clinics) - Global Forecast to 2023
Janos Haits

ENCODE Project at UCSC - 0 views

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    The Encyclopedia of DNA Elements (ENCODE) Consortium is an international collaboration of research groups funded by the National Human Genome Research Institute (NHGRI). The goal of ENCODE is to build a comprehensive parts list of functional elements in the human genome, including elements that act at the protein and RNA levels, and regulatory elements that control cells and circumstances in which a gene is active.
anonymous

Staphylococcus Aureus Project Report - Trivedi Science - 0 views

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    Genomic DNA was isolated from Staphylococcus aureus samples provided by Mahendra Trivedi and sub cultured samples provided by Bangalore Genei using Ultrapure Genomic DNA prep Kit.
Janos Haits

Home | 1000 Genomes - 0 views

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    A Deep Catalog of Human Genetic Variation
Walid Damouny

A better genetic test for autism - 2 views

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    "A large study from Children's Hospital Boston and the Boston-based Autism Consortium finds that a genetic test that samples the entire genome, known as chromosomal microarray analysis, has about three times the detection rate for genetic changes related to autism spectrum disorders (ASDs) than standard tests. Publishing in the April issue of Pediatrics (and online March 15), the authors urge that CMA become part of the first-line genetic work-up for ASDs."
anonymous

Introduction To Dna Fingerprinting - 1 views

We read and see a lot of news reports where the police seemed to have solved a murder case by the blood or hair strand left behind by the criminal. It is all possible thanks to DNA fingerprinting o...

DNA fingerprinting genetics research

started by anonymous on 06 Jan 15 no follow-up yet
Erich Feldmeier

Lisa Thalheim Weddimg Berlin Genforschung - Herumstochern im Genom - Wissen -... - 0 views

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    "In einer Kammer, kaum mehr als zwei mal drei Meter groß, einer früheren Toilette, findet man Lisa Thalheims Labor. Ein paar Meter weiter schrauben andere an Fahrrädern, Lisa Thalheim ist hier aber einem genetischen Fingerabdruck auf der Spur. Das Stadtbad Wedding ist einer der ersten Orte in Deutschland, an dem Autodidakten wie sie ihrer Liebe zur Gentechnik nachgehen können. "Software des Lebens" "Eine große Zukunft für die Biotechnologie-Industrie", hat der in Amerika als Naturwissenschafts-Papst verehrte Freeman Dyson vor fünf Jahren in der New York Review of Books vorhergesagt. Wenn sie dem Weg der Computerindustrie folge, "wenn sie klein und häuslich wird, statt groß und zentralisiert." Das scheint nun zu geschehen."
Erich Feldmeier

DIYgenomics - 0 views

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    "Nature: "A group called DIYgenomics has banded together to analyse their genomes, and even conduct and participate in small clinical trials" - October 2010 Nature Medicine: "...early adopters are showing how empowering and beneficial to science personal genetic information can be" - September 2010 WIRED: "...they wanted to build a model trial that could be easily replicated by citizen scientists anywhere" "
Erich Feldmeier

Fred H. Gage and Alysson R. Muotri Jumping Genes in the Brain Ensure That Even Identica... - 0 views

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    "So-called jumping genes, segments of DNA that can copy and paste them­selves into new places in the genome, can alter the activity of full-length genes. Occasionally they will turn on neighboring genes in these locations. That activity occurs more in the brain than other areas, resulting in different traits and behaviors, even in closely related individuals. These mobile genetic elements may also turn out to play a role in people's disposition to psychiatric disorders"
Janos Haits

CloudBioLinux - 0 views

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    CloudBioLinux offers genome analysis resources for cloud computing platforms such as Amazon EC2. We develop freely available, community maintained software images and data repositories for biological analysis.
Janos Haits

CHB - 0 views

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    Come work with us Interested in working with researchers from different disciplines within the Harvard, MIT and Broad community and an unique opportunity to participate in world-class research to make an impact on human health? Come work with us! We are looking for a computational biologists to handle data from a wide variety of experimental methods, focusing on next-gen sequencing technologies. Keep Reading...  SCDE is live The Stem Cell Discovery Engine (SCDE) is an integrated platform that allows users to consistently describe, share and compare cancer and tissue stem cell data. It is made up of an online database of curated experiments coupled to a customized instance of the Galaxy analysis engine with tools for gene list manipulation and molecular profile comparisons. The SCDE currently contains more than 50 stem cell-related experiments. Each has been manually curated and encoded using the ISA-Tab standard to ensure the quality of the data and its annotation. Keep Reading...  The Center for Health Bioinformatics at the Harvard School of Public Health provides consults to researchers for the management, integration and contextual analysis of biological high-throughput data. We are a member of the Center for Stem Cell Bioinformatics, the Environmental Statistics and Bioinformatics Core at the Harvard NIEHS Center for Environmental Health and the Genetics & Bioinformatics Consulting group for Harvard Catalyst and work closely with our colleagues in the Department of Biostatistics and the Program in Quantitative Genomics to act as a single point of contact for computational biology,
Janos Haits

Synthetic Biology Open Language - 0 views

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    Synthetic Biology Open Language (SBOL) is a software standard for the electronic exchange of specifications and descriptions of genetic parts, devices, modules, systems, and engineered genomes.
Erich Feldmeier

Google+, Great inventions and innovations overlapping edges of 2 or more disciplines - 0 views

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    "Great inventions and innovations were nearly always @ the overlapping edges of 2 or more disciplines, e.g. optics / microscope: http://ed.iiQii.de/gallery/VictimsOfGroupThink/PersistenceOfMemory_wikipedia_org But think to IT 1) human genome project / Craig Venter and to socialmedia 2) http://coturnix.org/ 3) http://scientopia.org/blogs/scicurious/ 4) http://michaelnielsen.org/blog/reinventing-discovery/ 5 ) „Science is an assault on ignorance, Its legacies are concepts,technologies and databases. As with many walks in life, the most glamorous legacies tend to get the most attention and the least are neglected" http://socrates.berkeley.edu/~scotch/maureretal_nature.pdf"
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