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Autel Best Scanner Maxisys MS909 Reviews

Posté le 4/3/2021 à 14:15 - 0 Commentaires - poster un commentaire - Lien

The Maxisys MS909 is a 10-inch TFT-LCD screen with a high-resolution capacitive touch screen tablet. MaxiSYS MS909 has the Android 7.0 operating system and the comprehensive OE-level vehicle coverage, with an octa-core processor (2.3GHz Quad + 1.7GHz Quad) and 128GB of RAM. Its functions are mainly used for diagnostic guidance and testing components to confirm maintenance. The MS909 is equipped with a combination of VCI and vehicle communication tools -- MaxiFlash VCI -- to provide faster dual Wi-Fi vehicle and network communications. It also has front and rear cameras and a rechargeable lithium-ion battery that lasts up to eight hours.
Best Autel Professional Car Diagnostic Tool: Autel Maxisys MS909 vs Maxisys Elite vs MS919 vs Maxisys Ultra comparison Chart
Autel Maxisys MS909 BULLET POINTS
Compatibility: it supplied with MaxiFlash VCI with Enhanced Protocol Compatability, which supports D-PDU, RP1210, CANFD. J2534 and DoIP protocols.
All New Software Specialist Capabilities: Repair Assist, DTC Analysis, Topology Mapping, and Relevant Cases.
Save Time: Quick boot-up time, view real-time data, See: entry level diagnostic tool. and use bi-directional control while not being bound by a cord.
Easy to Use:Even right out of the box, minimal setup was involved. Once the scan tool arrived in the shop ,it only needs to register the device on Autel’s website in order to perform updates. If you choose to not update it, you can use it out of the box within five minutes.”
Good Use Experience:10 inch TFT-LCD touchscreen for swift diagnosis and optimum viewing. The touchscreen is resistant to dirt and oil and the hard rubber surface is treated with high-quality carbon fiber, making the surface texture more refined.
More information: Autel Best Scanner ms909 : https://www.obd2reviews.com/autel-best-scanner-maxisys-ms909-reviews/

Study Sequences 64 Full Human Genomes Around the Globe | IE

Posté le 1/3/2021 à 01:12 - 0 Commentaires - poster un commentaire - Lien

Researchers at the University of Maryland School of Medicine (UMSOM) have published a new study that details the sequencing of 64 full human genomes from individuals around the world to better capture the genetic diversity of the human species.
"We've entered a new era in genomics where whole human genomes can be sequenced with exciting new technologies that provide more substantial and accurate reads of the DNA bases," said study co-author Scott Devine, Ph.D., Associate Professor of Medicine at UMSOM and faculty member of IGS.
"This is allowing researchers to study areas of the genome that previously were not accessible but are relevant to human traits and diseases."
The sequencing has many applications including enabling population-specific studies on genetic predispositions to human diseases as well as the discovery of more complex forms of genetic variation. The new dataset reflects 64 assembled human genomes that represent 25 different human populations from across the world.
The novel dataset was obtained using a combination of advanced sequencing and mapping technologies. As such, it better captures genetic differences from different human populations because each of the genomes was assembled without guidance from the first human genome composite.
"The landmark new research demonstrates a giant step forward in our understanding of the underpinnings of genetically-driven health conditions," said E. Albert Reece, MD, Ph.D., MBA, Executive Vice President for Medical Affairs, You may need: diagnostic code reader. UM Baltimore, and the John Z. and Akiko K. Bowers Distinguished Professor and Dean, University of Maryland School of Medicine.
"This advance will hopefully fuel future studies aimed at understanding the impact of human genome variation on human diseases."
The International Human Genome Sequencing Consortium announced the first draft of the human genome reference sequence twenty years ago this month. It was called The Human Genome Project.
The study is published on Science.
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