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- Another important method of linkage analysis is the Affected Sib Pair (ASP). 連鎖分析的另一種重要統計方法是生病同胞對法(ASP)。
- Methods The parameter linkage analysis of the small pedigree data was used. 方法運用小家系資料連鎖分析參數的方法。
- RFLP Linkage Analysis and deletion analysis in one family with BMD and two families with DMD. 一個(gè)BMD和二個(gè)DMD家系的RFLP連鎖分析和缺失分析
- This information is valuable both as a prelude to linkage analysis, which generally assumes Mendelian transmission. 這一信息有利于進(jìn)一步所做的連鎖分析。
- Objective To identify the disease locus in X-linked retinitis pigmentosa (RP) families using genetic linkage analysis. 目的應用遺傳連鎖分析方法對X連鎖型視網(wǎng)膜色素變性家系進(jìn)行分析,定位其致病基因的所在位點(diǎn)。
- Selection is practically ubiquitous during marker-QTL linkage analysis with an experimental population. 從實(shí)際角度看，選擇在用于標記-QTL連鎖分析的實(shí)驗群體中是較普遍存在的。
- Objective To identify the disease locus in X-linked retinitis pigmentosa(XLRP) families using genetic linkage analysis. 目的應用遺傳連鎖分析方法對X連鎖型視網(wǎng)膜色素變性家系進(jìn)行分析,確定其致病基因的所在位點(diǎn)。
- Meanwhile,the method of gene linkage analysis and that of using oligonucleotide probe are compared. 同時(shí)將基因的連鎖分析法與寡核苷酸法進(jìn)行了比較。
- This STR linkage analysis can identify the molecular defect of PWS cases quickly and accurately. STR連鎖分析是一種可準確診斷PWS并明確其分子缺陷類(lèi)型的好方法；
- But no pathogenetic gene has been cloned. To refine the location of CMN, we had research on a Chinese pedigree of CMN through genescan and linkage analysis. 我們擬應用基因組掃描技術(shù)，通過(guò)連鎖分析對一個(gè)來(lái)自于浙江溫州的CMN家系進(jìn)行相關(guān)致病基因的染色體定位研究。
- Recently, with using of whole genome genotyping and linkage analysis, some chromosome regions have been related to human dermatoglyphic patterns. 特別是最近幾年，通過(guò)全基因組基因分型和連鎖分析，在染色體上得到了一些和膚紋特征相關(guān)的基因候選區域。
- Objective To study the clinical application value of genetic linkage analysis for bronchial asthma with two STRs-D5S436 and D5S658. 目的探索短串聯(lián)重復序列-D5S436和D5S658在支氣管哮喘家系連鎖分析中的應用價(jià)值。
- Haplotype and linkage analysis indicate that the Ashkenazi haplotypes is not associated with HMPS in Singapore Chinese families,which suggests genetic heterogeneity. 單倍型及遺傳連鎖分析提示,Ashkenazi單倍型與華人HMPS無(wú)關(guān),兩者存在遺傳背景的差異性。
- The two-locus, non-parametric linkage analysis (NPL), maximum LOD score and transmission/disequilibrium test (TDT) with GENEHUNTER program were used in this study. 統計采用GENEHUNTER軟件包兩點(diǎn)非參數連鎖（NPL）分析、計算優(yōu)勢對數記分(Lod)值及傳遞不平衡檢驗（TDT）。
- First half focuses on human genetics and molecular biology, covering fundamentals of pedigree analysis, linkage analysis, molecular cloning, and gene analysis as well as ethical/ legal issues, all in the context of an auditory disorder. 前半段會(huì )著(zhù)重于人類(lèi)遺傳學(xué)與分子生物學(xué)，涵蓋家族系譜分析、鎖分析、子選殖、因分析與道德法律議題的基礎概述，并且皆以聽(tīng)覺(jué)系統疾病為例來(lái)說(shuō)明。
- Simulation study and real data analysis were performed using SAS/IML software, and the validity and practicability of Bayesian method in genetic linkage analysis were thus verified. 用編制的SAS/IML程序進(jìn)行了模擬研究和實(shí)例分析，驗證了貝葉斯方法在遺傳連鎖分析中的有效性和實(shí)用性。
- Aim:To set up a method of prenatal diagnosis of classic phenylketonuria ( PKU) by linkage analysis of the short tandem repeat(STR) in intron 3 linked to the phenylalanine hydroxylase (PAH) gene. 目的:建立一種利用苯丙氨酸羥化酶(PAH)基因內含子3中短串聯(lián)重復序列(STR)多態(tài)性連鎖分析進(jìn)行經(jīng)典型苯丙酮尿癥(PKU)產(chǎn)前診斷的方法。
- Model-independent sib-pair linkage analyses and tests of association were performed to analyze the genetic effects of the exon 12 polymorphism. 個(gè)體模型同胞配對后，通過(guò)進(jìn)行連鎖分析和關(guān)聯(lián)實(shí)驗，來(lái)分析外顯子12多態(tài)現象的遺傳效應。
- Thus, it is necessary to investigate the impacts of selection upon linkage analyses in order to obtain unbiased estimates of QTL position and effect. 為獲得QTL位置及其效應的無(wú)偏估計，有必要研究選擇對連鎖分析實(shí)驗所造成的影響。
- We present here four non-parametric statistics for linkage analysis (APM,SIBPAL,MAPMAKER-SIB and GENEHUNTER-NPL).Using the simulated pedigrees,we introduced the usage of these methods. 非參數連鎖分析是進(jìn)行復雜疾病連鎖分析的有效手段,本文通過(guò)擬合的數據資料,對目前廣泛使用的非參數型連鎖分析方法進(jìn)行了探討,為今后有針對性的選擇連鎖分析方法提供依據。
