• I first had a list of size 8, then 4, then 2, but then I had another problem of size 2.

    首先是一个8个元素的序列,接着变成了4个元素,接着2个元素,然后我就碰到了2个元素的另一个问题。

    哈佛公开课 - 计算机科学课程节选

  • Well here is my array of 8, you know what, it's too much work to sort all 8.

    这是8个杯子的一个序列,要对这8个杯子进行排序就会花费较大功夫。

    哈佛公开课 - 计算机科学课程节选

  • That creates a problem in the genetic code in that there's 64 possible sequences but there's only 20 some amino acids, so each amino acid can be specified by more than one codon.

    这里个问题,遗传密码六十四种可能的序列,而只二十种氨基酸,因此每种氨基酸都,不止一种密码子与之对应

    耶鲁公开课 - 生物医学工程探索课程节选

  • When you look at a random walk you have the intuitive impression that you can extrapolate it -that it doesn't look like -you can't believe it's really random, but the reason you can't is because you overweigh the probability of certain things that caught your attention.

    当人们观察随机漫步序列时会直观印象,并可以以此类推,虽然这看起来并不像...,人们不会觉得这是完全随机的,之所以如此,是因为,人们过分高估了特定事物发生的可能性,这吸引了人们的注意

    耶鲁公开课 - 金融市场课程节选

  • So here is a list of size 2, this is the light one, this is the heavier one.

    这是2个元素的一个序列,这杯轻一些,这杯重一些。

    哈佛公开课 - 计算机科学课程节选

  • Who cares if I randomly send him or her elsewhere in the array?

    就算我把他或者她排在序列中的其他位置,又谁会在意呢?

    哈佛公开课 - 计算机科学课程节选

  • It's only going to bind to fragments that contain that piece of the gene, and it will make those visible to you in some way so you can see where your gene traveled.

    它只会和那段序列的片段结合,从而能让你看到那段片段在哪里,你就可以知道目标基因片段到了哪个位置

    耶鲁公开课 - 生物医学工程探索课程节选

  • And so now when I have the list here, let's see, yours is facing this way, so small is gonna be here large is gonna be here.

    现在了这个序列,你们是面向这边的,那小的放这边,大的放这边。

    哈佛公开课 - 计算机科学课程节选

  • That might be a good way to do it but it's going to be more of a challenge because you might - you're going to have a lot of these non-coding sequences that are in the way.

    这或许是个好方法,但这会带来更大的问题,因为也许--,会许多不编码蛋白质的序列,干扰你的筛选

    耶鲁公开课 - 生物医学工程探索课程节选

  • For example, this transfer RNA has a unit here, at one end of the transfer RNA molecule.

    举个例子,这个tRNA的一端,一个GAG的碱基序列单元

    耶鲁公开课 - 生物医学工程探索课程节选

  • When you think about a gene or a transcript, the messenger RNA copy of a gene, you know that for every sequence of a nucleic acid there's a complimentary sequence.

    当你们考虑一段基因或者一个,转录一段基因的mRNA拷贝,你们知道每个核酸序列,都互补序列

    耶鲁公开课 - 生物医学工程探索课程节选

  • Well one way you could do it is by saying 'if I have this one base pair difference then this sequence is going to be cut by a specific restriction enzyme that recognizes the sequence CTGAGGA'.

    一种方法是通过考虑,"如果我这个不同的碱基对,那该序列必然会,被特定的限制酶识别并切割,这个特定的限制酶能识别,CTGAGGA "

    耶鲁公开课 - 生物医学工程探索课程节选

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