reassignment SAMSUNG ELECTRO-MECHANICS CO. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.) Filing date Publication date Priority claimed from KR2002-73213 external-priority Application filed by Samsung Electro Mechanics Co Ltd filed Critical Samsung Electro Mechanics Co Ltd Assigned to SAMSUNG ELECTRO-MECHANICS CO.
Original Assignee Samsung Electro Mechanics Co Ltd Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.) ( en Inventor Keun-Woo Park Jong-Sik Jeong Kyoung-Joong Min Kang-ju Kim Byoung Won Hwang Won-Tae Choi Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.) Expired - Fee Related, expires Application number US10/414,689 Other versions US20040100444A1
#PROCESSSING PMOUSE AND MOUSE PDF#
Google Patents Method of processing data of optical mouseĭownload PDF Info Publication number US7079116B2 US7079116B2 US10/414,689 US41468903A US7079116B2 US 7079116 B2 US7079116 B2 US 7079116B2 US 41468903 A US41468903 A US 41468903A US 7079116 B2 US7079116 B2 US 7079116B2 Authority US United States Prior art keywords frame image present axis direction nth frame Prior art date Legal status (The legal status is an assumption and is not a legal conclusion. Google Patents US7079116B2 - Method of processing data of optical mouse The paper is published in the journal Nature Structural & Molecular Biology.US7079116B2 - Method of processing data of optical mouse "Now we have more comprehensive understanding of the different layers of -omics in early embryo development." This study fills a gap in the transcriptome field and sets up researchers to look further into the function of m 6A during development, said Au. They also found m 6A distribution in so called transposable elements, previously thought to be 'junk' because they do not encode proteins, in the developing embryo. Together with his collaborators Arne Klungland, Ph.D., and John Arne Dahl, Ph.D., of Oslo University in Norway, his team accomplished their study by pooling together mouse embryos at six developmental stages, generating transcriptome-wide m 6A maps for each.ĭoing so, they discovered intriguing patterns of m 6A modification on genes inherited from the mother versus those activated from the developing embryo. For example, the amount of RNA being studied is measured in picograms, one-trillionth of a gram. "Because of the limited amount of cellular material in early embryonic development, it is very challenging to map m 6A modification," said Au. of the Department of Computational Medicine and Bioinformatics, has successfully constructed the landscape of m 6A in a mouse embryo, one of the last frontiers for mapping m 6A modification. Research from University of Michigan Medical School's Kin Fai Au, Ph.D. Having this readout can tell scientists when genes are turned off and on in a cell, deciding in large part the cell's ultimate fate. Scientists over the past decade have revealed that the m 6A modification has a wide variety of functions, from the programming of cells to the development of embryos.Ī major goal for researchers in the field of computational medicine has been to describe the transcriptome-the sum of all of the RNA readouts of a cell-including modifications like m 6A. One of the most common and important RNA modifications in animal cells is called N 6-methyladenosine, or m 6A. Before this happens, however, the RNA is modified to make it more stable and mature. Its typical job in an organism is to take the genetic material coded in the DNA inside a cell's nucleus into the interior of the cell where it is transformed into proteins that carry out different functions in the body.
0 kommentar(er)
