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Show Karl Gordon Lark down, it could be 6 offby quite a bit. And yet, it looked like it pursue this. Of course, Karen Miller clinical organizer. was heritable. So, was ecstatic and she became She would get materials. So we our September 2015 we decided to project organizer for years, got blood from dogs and began looking at DNA genotypes. said to Elaine Ostrander enters the point, At this Karen, if we really start this, is anybody doing veterinarian she knew. That veterinarian conjunction with Elaine markers, we used, these originally, as were You What you used was use ones was was getting this sequence these associated with something thought let's complicated, go after much dog genetics. so more that we use those something. dog quantitative much was us ones Ray White used one and you could and see had available differences. called PCR segment and these segments would genetic markers So Elaine dog behavior. complex, as a a working in by then well established, technique and you get bit. I identify them could repeat markers, SSR. They're however a She mentioned used in the human genome because that's what We could about in, well, I'll back up all of his gene markers and numbers of sequences relatively new, dog to dog. to find out serious was in Seattle. So I wrote to Elaine and she sent amplify up using particular sequences were Elaine electrophoresis to separate the products differ from and large called, simple similar to the techniques. and you Ostrander. She sequences of markers, scene. and then could we measuring qualitative see how well traits. Her goal was We'd been working with soybean quantitative traits traits. So whole more a new ballgame interesting for him, so we for Kevin, much more began working with that. We have department. this. The So one a colleague who is a functional morphologist, Dave he, Kevin, I and Fred Adler, Elaine Ostrander and is in Seattle just giving us markers and 18 we were Carrier, here in the one of her doing all people worked the rest. What we on did was |
