d.n.a. sequencing is the first of its kind to be used in the middle east this is a third generation sequencer and what it does is it sequences or fragments of the genetic code this one can give us as you see here the tail goes all the way to forty thousand forty thousand as a model to one handwriting that one so that will give you more structure information in the chromosome this equipment makes it possible for the lab to sequence the gene. knowns of large numbers of people it's a huge advance since nine hundred ninety when the first projects to sequence the human genome officially began their original human genome reference was sequenced in ten years it was a huge international feeling it was a big accomplishment and now we can sequence the human genome within six to ten days with this technology so that addresses are huge within ten years. going on here puts the university at the forefront of modern research building on the stunningly spirit of the golden age were over a thousand years ago the flow was from the west to the arab world where people were coming to. sandra in damascus centers o

d.n.a. sequencing is the first of its kind to be used in the middle east this is a third generation sequencer and what it does is it sequences are fragments of the genetic code this one can give us as you see here the tail goes all the way to forty thousand forty thousand as a model to one hand about being that one so that will give you more structure information on the chromosome this equipment makes it possible for the lab to sequence the gene. knowns of large numbers of people it's a huge advance since nine hundred ninety when the first projects to sequence the human genome officially began their original human genome reference was sequenced in ten years it was a huge international feeling it was a big accomplishment and now we can sequence the human genome within six to ten days with this technology so that addresses are huge within ten years. going on here puts the university at the forefront of modern research building on the scholarly spirit of the golden age where over a thousand years ago the flow was from the west to the arab world where people were coming to. the xandra in damascus

these diseases is to analyze people's genomes to look for differences and to do this they use a d.n.a. sequence or connected to a supercomputer all living organisms i made up of cells each cell has a nucleus and within the new pieces the genetic material that defines the features that make a few of. these genetic material is a code made up of over three billion components called bases. is too long to be analyzed in one piece so first they need to split it into smaller sections these machines is does a process called shotgun sequence so essentially here what we do is take that genetic material chop it up into small pieces and load it into the instrument it will and chirp read the information and put these pieces back together so rather than trying to follow the full string awful but the billions of bases on one d.n.a. molecule is chopping it up looking at different bits and then putting it back piecing it back together genetic technology is evolving rapidly the lab has recently installed their most advanced piece of equipment for d.n.a. sequencing is the first of its kind to be used in the middl

a cool talons come the d.n.a. sequence to suppress surface receptor. can then be targeted for specific cancer so now you have this is the time of the impressions of the two sounds in the next city and now the action to get your reaction to the story now i'm joined in the next hour to three hours old the genetic tangle have the trucks only for ninety percent of the cells will get the genetic thing not hundred percent. you caught nineteen later richards he had acute lymphoblastic leukemia a our form of cancer. you caught one two three targets eight and out were acute myeloid leukaemia own mary cancer. so what do we have half so these are. the cells are targeting acute lymphoblastic leukaemia and they have been told so they were frozen and without them and so we can see the cells. wow there are many council soldiers in there it's amazing to think that one of these tiny little sounds is a cancer. yeah when you see them actually. credit. the idea behind this therapy is to make it viable for any patient because the t. cells are not specific to an individual

so cool talons come the d.n.a. sequence to suppress certain surface receptor. sounds can then be targeted for specific cancer so now what you have is the time and the impressions of the two sounds to me that you're sitting on now the action against your reaction to storing now and during the next two hours to three hours old a genetic thing will have the trucks hauling for ninety percent of the cells will get the genetic thing not hundred percent. you can't nineteen is useful later richards he had acute lymphoblastic leukemia a our form of blood cancer. you can't one two three targets eight am for acute myeloid leukemia don't marry cancer. so what do we have so these are t. cells. cells are targeting. and they have been just so they were frozen and we thought them. so we can see the cells. wow there are many cancer soldiers in there it's amazing to think that one of those tiny in the core sounds is a cancer fighter when you see them and actually incredible the idea behind this therapy is to make it viable for any patient because the t. cells are not specific to