Estimating the fraction of invariable codons with a capture-recapture method
β Scribed by Arend Sidow; Trang Nguyen; Terence P. Speed
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 677 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0022-2844
No coin nor oath required. For personal study only.
β¦ Synopsis
A codon-based approach to estimating the n u m b e r of variable sites in a protein is presented. When first and second positions of codons are assumed to be replacement positions, a capture-recapture model can be used to estimate the n u m b e r of variable codons from every pair of homologous and aligned sequences. The capture-recapture estim a t e is c o m p a r e d to a m a x i m u m likelihood estimate of the n u m b e r of variable codons and to previous approaches that estimate the n u m b e r of variable sites (not codons) in a sequence. C o m p u t e r simulations are presented that show under which circumstances the capture-recapture estimate can be used to correct biases in distance matrices. Analysis of published sequences of two genes, calmodulin and serum albumin, shows that distance corrections that e m p l o y a capture-recapture estimate of the n u m b e r of variable sites m a y be considerably different f r o m corrections that assume that the n u m b e r of variable sites is equal to the total n u m b e r of positions in the sequence.
π SIMILAR VOLUMES
A variety of methods have been proposed to estimate the size of a closed population non-parametrically using capturerecapture data when the capture probabilities are heterogeneous. None of the methods have been proven to be unbiased in all circumstances and in simulations they tend to perform well i
## Abstract A modification of the erythrocyte partitioning method for the rapid estimation of plasmaβfree drug fractions (__f__~u~) is described and applied to five basic drugs. In the procedure, which uses readily available clinical laboratory equipment, __f__~u~ is calculated from measurements of