M****e
发帖数: 70 | 1 I was listening to a speech given by J. Craig Venter the other day. It was a
very impressive one, though it was much more like elementary education to the
general audience. One thing that really impressed me is the expressed sequence
tags technology (ESTs), which was developed and applied by J. Craig Venter to
discover a multitude of new genes and consequently integrated into the Human
Genome Project. The explosion of discovering new genes with the help of
mathmatics and computers was realized o | p*******r
发帖数: 4048 | 2 Well, it depends on how long the EST is then. It also depends on the library
the EST is built from. If the normalization is not very good, you will miss
genes that are not highly expressed.
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【在 M****e 的大作中提到】
: I was listening to a speech given by J. Craig Venter the other day. It was a
: very impressive one, though it was much more like elementary education to the
: general audience. One thing that really impressed me is the expressed sequence
: tags technology (ESTs), which was developed and applied by J. Craig Venter to
: discover a multitude of new genes and consequently integrated into the Human
: Genome Project. The explosion of discovering new genes with the help of
: mathmatics and computers was realized o
| c**********c
发帖数: 5 | 3 Your concern is exactly the key limitation of this technology. The advantage of EST is that it provides direct evidence of the expression of a gene. But several drawbacks I could think of:
1. mRNA abundance limitation: it is estimated that genes have an average expression level below 5% of the mRNA population is less likely to be detected by EST technology. Therefore, genes that are expressed at extreme low level won't be able to be detected by EST, so the 27K in this sense should be an lower es |
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