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收缩压在17号染色体上进行连锁检测时纵向方差成分与基于回归方法的比较。

Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressure.

作者信息

de Andrade Mariza, Olswold Curtis

机构信息

Division of Biostatistics, Department of Health Sciences Research, Mayo Clinic, 200 First Street, SW, Rochester, Minnesota, USA.

出版信息

BMC Genet. 2003 Dec 31;4 Suppl 1(Suppl 1):S17. doi: 10.1186/1471-2156-4-S1-S17.

Abstract

We compare two methods to detect genetic linkage by using serial observations of systolic blood pressure in pedigree data from the Framingham Heart Study focusing on chromosome 17. The first method is a variance components (VC) approach that incorporates longitudinal pedigree data, and the second method is a regression-based approach that summarizes all longitudinal measures in one single measure. No evidence of linkage was found either using the VC longitudinal approach or the regression-based approach, except when all time points were used from Cohorts 1 and 2 and only subjects aged 25 and 75 years were included.

摘要

我们比较了两种利用弗明汉心脏研究中关于17号染色体的家系数据收缩压的系列观察来检测基因连锁的方法。第一种方法是纳入纵向家系数据的方差成分(VC)法,第二种方法是基于回归的方法,该方法将所有纵向测量汇总为一个单一测量值。无论是使用VC纵向方法还是基于回归的方法,均未发现连锁证据,除非使用队列1和队列2的所有时间点且仅纳入年龄为25岁和75岁的受试者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e57a/1866451/77453024b721/1471-2156-4-S1-S17-1.jpg

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