Category Archives: Transhuman News

Arginase Deficiency - A Bibliography And Dictionary For Physicians, Patients, And Genome Researchers
ll4.me Arginase Deficiency - A Bibliography And Dictionary For Physicians, Patients, And Genome Researchers - Icon Health Publications This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Arginase deficiency. It also gives extensive lists of bibliographic citations. Finally, it provides information to users on how to update their knowledge using various Internet resources. The book is designed for physicians, medical students preparing for Board examinations, medical researchers, and patients who want to become familiar with research dedicated to Arginase deficiency. If your time is valuable, this book is for you. First, you will not waste time searching the Internet while missing a lot of relevant information. Second, the book also saves you time indexing and defining entries. Finally, you will not waste time and money printing hundreds of web pages.Author: ICON Health Publications Publisher: ICON Health Publications Illustration: N Language: ENG Title: Arginase Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers Pages: 00112 (Encrypted PDF) On Sale: 2007-07-19 SKU-13/ISBN: 9780497113346 Category: Medical : Diseases This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Arginase deficiency. It also gives extensive lists of bibliographic citat icon health publications, medical, diseasesFrom:AprilCadeJumpViews:0 0ratingsTime:00:12More inPeople Blogs

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Transposable elements
For more information, log on to- shomusbiology.weebly.com Download the study materials here- shomusbiology.weebly.com A transposable element (TE) is a DNA sequence that can change its position within the genome, sometimes creating mutations and altering the cell #39;s genome size. Transposition often results in duplication of the TE. Barbara McClintock #39;s discovery of these jumping genes early in her career earned her a Nobel prize in 1983.[1] TEs make up a large fraction of the C-value of eukaryotic cells. They are generally considered "junk DNA". In Oxytricha, which has a unique genetic system, they play a critical role in development.[2] They are also very useful to researchers as a means to alter DNA inside a living organism. Class I (retrotransposons): They copy themselves in two stages, first from DNA to RNA by transcription, then from RNA back to DNA by reverse transcription. The DNA copy is then inserted into the genome in a new position. Reverse transcription is catalyzed by a reverse transcriptase, which is often coded by the TE itself. Retrotransposons behave very similarly to retroviruses, such as HIV. There are three main orders of retrotransposons (other orders are less abundant): Those with long terminal repeats (LTRs): encode reverse transcriptase, similar to retroviruses; LINEs: encode reverse transcriptase, lack LTRs, transcribed by RNA polymerase II; SINEs: do not code for reverse transcriptase, transcribed by RNA polymerase III. Retroviruses can be ...From:Suman BhattacharjeeViews:1 0ratingsTime:09:07More inEducation

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Mammalian Brain Development
ll4.me Mammalian Brain Development Table of Contents: - Sexual differentiation of the brain: genetic, hormonal, and trophic factors- Hugo F. Carrer; Mara J. Cambiasso- Life at the interface between a dynamic environment and a fixed genome: Epigenetic programming of stress responses by maternal behavior- Ian Weaver, PhD- Effects of early life seizures and anti-epileptic drug treatment on brain development in human models- Amy Brooks-Kayal, MD; Eric Marsh, MD, PhD- Prenatal development of the human blood-brain barrier- Luca Cucullo, PhD- Seizure propensity and brain development: a lesson from animal models- Annamaria Vezzani, PhD; Jana Veliskova, PhD; Astrid Nehlig, PhD- Seizures and antiepileptic drugs: does exposure alter normal brain development in animals models?- Solomon Moshe, MD; Libor Velisek, MD, PhD; Aristea Galanopoulou, MD, PhD- Overview of neural mechanisms of developmental disorders- Ayush Batra; Dr. Kathleen Franco; Erin Carlton- Drug permeation across the fetal maternal barriers- Chaitali Ghosh; Nicola Marchi, PhD- In vivo imaging of brain development: Technologies, models, applications, and impact on understanding the etiology of mental retardation- Vicko Gluncic, MD- Congenital, non-inheritable chromosomal abnormalities responsible for neurological disorders- Patrizia D #39;Adamo and Riccardo Bianchi, PhD EAN/ISBN : 9781607612872 Publisher(s): Springer, Berlin, Humana Press Format: ePub/PDF Author(s): Janigro, Damir Table of Contents: - Sexual differentiation ...From:ChrisRomeoJacksonViews:0 0ratingsTime:00:14More inPeople Blogs

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Reading the book of life: Pol van Dorpe at TEDxUHasselt
Sequencing the human genome has been possible for quite a while, but has always been very expensive. Pol van Dorpe is working on technology that #39;s about to change this and will make it affordable for everyone. In this talk, Pol van Dorpe explains how this technology will change the world. Pol Van Dorpe is currently active as a principal scientist at Imec, Leuven and part time professor at the physics department of the KULeuven. In 2006, he obtained his PhD at the faculty of engineering of the KULeuven in 2006, after which he was appointed as a postdoctoral fellow of the FWO-Flanders (2006-2012), based in Imec, and focused on metal based nanophotonics, or plasmonics for biosensors and energy harvesting. During this period he worked for some time in Stanford University and he set up world-wide collaborations with renowned scientists in this field. His work has led to over 50 peer-reviewed papers in high impact factor journals and has attracted more than 1000 citations. Currently he is active in the bio-nano-electronics department of Imec and his main research focus is applying nanophotonics concepts to create new ways to unravel the sequence of the DNA, ie the genetic code. In thespirit of ideas worth spreading, TEDx is a program of local, self-organized events that bring people together to share a TED-like experience. At a TEDx event, TEDTalks video and live speakers combine to spark deep discussion and connection in a small group. These local, self-organized events are ...From:TEDxTalksViews:51 3ratingsTime:12:37More inNonprofits Activism

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Tetrahydrobiopterin Deficiency - A Bibliography And Dictionary For Physicians, Patients, And Genome
ll4.me Tetrahydrobiopterin Deficiency - A Bibliography And Dictionary For Physicians, Patients, And Genome Researchers - Icon Health Publications This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Tetrahydrobiopterin deficiency. It also gives extensive lists of bibliographic citations. Finally, it provides information to users on how to update their knowledge using various Internet resources. The book is designed for physicians, medical students preparing for Board examinations, medical researchers, and patients who want to become familiar with research dedicated to Tetrahydrobiopterin deficiency. If your time is valuable, this book is for you. First, you will not waste time searching the Internet while missing a lot of relevant information. Second, the book also saves you time indexing and defining entries. Finally, you will not waste time and money printing hundreds of web pages.Author: ICON Health Publications Publisher: ICON Health Publications Illustration: N Language: ENG Title: Tetrahydrobiopterin Deficiency - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers Pages: 00108 (Encrypted PDF) On Sale: 2007-07-20 SKU-13/ISBN: 9780497113858 Category: Medical : Diseases This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Tetrahydrobiopterin deficiency. It also gives extensive lists of bibliogr ...From:NadiaLetnaunchynViews:0 0ratingsTime:00:14More inPeople Blogs

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Nucleic Acids And Proteins In Soil
ll4.me Nucleic Acids And Proteins In Soil From the contents- Introduction.- Chemical characterization of organic N and organic P.- Extraction of nucleic acids and proteins from soil.- Sources and fate of nucleic acids and proteins in soil.- Microbial diversity and soil functions.- Genome and gene transfer in soil.- Marker and reporter genes. EAN/ISBN : 9783540294498 Publisher(s): Springer, Berlin Discussed keywords: Boden, Nukleinsure, Protein Format: ePub/PDF Author(s): Nannipieri, Paolo - Smalla, Kornelia From the contents- Introduction.- Chemical characterization of organic N and organic P.- Extraction of nucleic acids and proteins from soil.- Sources and fate of nucleic acids and proteins in soil.- MFrom:AdamRadabaughMillerViews:0 0ratingsTime:00:13More inPeople Blogs

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Coffin-lowry Syndrome - A Bibliography And Dictionary For Physicians, Patients, And Genome Researche
ll4.me Coffin-lowry Syndrome - A Bibliography And Dictionary For Physicians, Patients, And Genome Researchers - Icon Health Publications This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Coffin-Lowry syndrome. It also gives extensive lists of bibliographic citations. Finally, it provides information to users on how to update their knowledge using various Internet resources. The book is designed for physicians, medical students preparing for Board examinations, medical researchers, and patients who want to become familiar with research dedicated to Coffin-Lowry syndrome. If your time is valuable, this book is for you. First, you will not waste time searching the Internet while missing a lot of relevant information. Second, the book also saves you time indexing and defining entries. Finally, you will not waste time and money printing hundreds of web pages.Author: ICON Health Publications Publisher: ICON Health Publications Illustration: N Language: ENG Title: Coffin-Lowry Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers Pages: 00116 (Encrypted PDF) On Sale: 2007-07-20 SKU-13/ISBN: 9780497113537 Category: Medical : Diseases This is a 3-in-1 reference book. It gives a complete medical dictionary covering hundreds of terms and expressions relating to Coffin-Lowry syndrome. It also gives extensive lists of bibliographic cit icon health publications, medical ...From:KennishaBrownViews:0 0ratingsTime:00:15More inPeople Blogs

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Genetically Engineered Salmon Safe, FDA Says
FDA says that genetically engineered salmon are safe. A species of genetically engineered salmon that grow faster than regular salmon are safe to eat and would not cause any environmental disruptions, according to a new report by the Food and Drug Administration, or FDA. The genetically modified fish, known as AquAdvantage salmon, can grow twice as fast as naturally born salmon, thanks to a growth hormone gene from the Chinook species that was added to the DNA genome of the altered salmon. If the FDA does approve the salmon for sale, it would be the first genetically modified animal product available on the US market, and could open the door for other genetically engineered meat projects to try and break onto the consumer market. Environmentalists are concerned that the modified salmon might overrun native species of fish if they were to accidentally be released into the wild, and skeptics say the tests that were performed on the fish to assess their safety were not adequate to fully understand the potential effects of the AquAdvantage salmon. Senator Mark Begish from Alaska said: "I will fight tooth and nail with my Alaska colleagues to make sure consumers have a clear choice when it comes to wild and sustainable versus lab-grown science projects." Do you think the genetically modified salmon should be available to consumers?From:GeoBeatsNewsViews:2 0ratingsTime:01:11More inNews Politics

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GAITHERSBURG, Md.--(BUSINESS WIRE)--

OpGen, Inc. today announced its ARGUS Whole Genome Mapping System technology was used in combination with next-generation sequencing (NGS) to produce the first, high-quality reference genome of the domestic goat. The study, which was led by BGI-Shenzhen and Kunming Institute of Zoology, Chinese Academy of Sciences was published online today in Nature Biotechnology. The paper, titled Sequencing and automated whole-genome optical mapping of the genome of a domestic goat (Capra hircus), demonstrates the value, efficiency and cost effectiveness of OpGens Whole Genome Mapping in de novo assemblies of large, complex genomes.

This independent technology provides not only the validation of the genome sequencing, but also provides the large-scale chromosome structure information that cannot be detected by sequencing, said Xun Xu, Deputy Director, BGI-Shenzhen. The experience in these genome assembly projects shows that the physical whole genome map should be the standard for any reference genome to be assembled in the future.

Goats are an important economic resource in many developing countries around the globe, including China and India. However, despite their agricultural and biological importance, breeding and genetic studies of goats have been hindered by the lack of a high-quality reference genome sequence. The goat genome is the first high-quality reference genome for small ruminate animals and may help to advance the understanding of distinct ruminant genomic features from non-ruminant species.

Although generating draft assemblies from NGS is relatively easy, finishing a sequence to the chromosome level is still difficult and costly. The findings show that a single NGS platform, when combined with Whole Genome Mapping, can produce a finished assembly much faster and less expensively than other currently available mapping strategies such as bacterial artificial chromosome (BACs) or fluorescence in situ hybridization (FISH). This approach sets the gold standard in large genome de novo assembly, eliminating the need for genetic maps which can be very time consuming.

By incorporating Whole Genome Mapping, we were able to overcome the limitations of NGS short read scaffolds to produce long super-scaffolds and finish the assembly to the near chromosome level, said Wen Wang, Deputy Director, Kunming Institute of Zoology, Chinese Academy of Sciences and an author of the paper. We could not have completed the project without OpGens technology.

In the study, OpGens ARGUS system produced 100,000 single molecule restriction maps in three hours. This resulted in 30 times the physical coverage of the goat genome. The companys Genome Builder software generated long super-scaffolds by combining single molecule map data with sequence scaffolds generated by NGS and subsequent assembly. Specifically, the metric of assembly (N50) was improved eightfold by combining Whole Genome Mapping with NGS over NGS alone.

While we continue to demonstrate the value of Whole Genome Mapping for assembly, quality control and validation of microbial genomes, we are pleased to expand its applications as a critical, complementary technology enabling investigators to provide complete and accurate long-range genomic information in complex, de novo projects, said Richard Moore, M.D., Ph.D., chief scientific officer of OpGen and an author of the paper. This paper is the first of many we expect to be published over the next year which will validate OpGens Whole Genome Mapping technology as a solution for the de novo assembly of the spectrum of genomes from microbes to mammals.

About ARGUSWhole Genome Mapping System

OpGens ARGUS Whole Genome Mapping System is the only commercially available technology that can provide a high-resolution, complete visual map of a whole genome and individual chromosomes. The companys unique single molecule analysis technology provides a whole genome view that complements genome assembly and enables scientists to identify highly repetitive regions, tandem repeats and translocations that are very difficult to identify and clarify with sequencing alone. Sequencing projects can now be finished and validated with less investment in time, cost and computational effort.

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OpGen Announces Sequence Assembly and Finishing of First Reference Genome of Domestic Goat