نتایج جستجو برای: haplotyping

تعداد نتایج: 559  

Journal: :Trends in genetics : TIG 2001
M A Jobling

Hereditary surnames contain information about relatedness within populations. They have been used as crude indicators of population structure and migration events, and to subdivide samples for epidemiological purposes. In societies that use patrilineal surnames, a surname should correlate with a type of Y chromosome, provided certain assumptions are met. Recent studies involving Y-chromosomal h...

Journal: :The Journal of Experimental Medicine 1973
J. A. van der Does J. J. van Rood W. S. Walker R. B. Epstein

A procedure of intrafamilial immunization is described for production of antisera recognizing DL-A haplotypes. In a colony consisting of 1 sire, 6 bitches, and 67 offspring all haplotypes could be accurately allocated. In the colony the observed reaction frequencies of the antisera are in agreement with mendelian codominant inheritance. Mixed lymphocyte culture tests confirmed the accuracy of t...

2016
Nicholas M. Murphy Matthew Burton David R. Powell Fernando J. Rossello Don Cooper Abha Chopra Ming Je Hsieh David C. Sayer Lavinia Gordon Mark D Pertile Brian D. Tait Helen R. Irving Colin W. Pouton

We describe a method for determining the parental HLA haplotypes of a single individual without recourse to conventional segregation genetics. Blood samples were cultured to identify and sort chromosome 6 by bivariate flow cytometry. Single chromosome 6 amplification products were confirmed with a single nucleotide polymorphism (SNP) array and verified by deep sequencing to enable assignment of...

Journal: :Journal of bioinformatics and computational biology 2008
Jing Li Tao Jiang

Two grand challenges in the postgenomic era are to develop a detailed understanding of heritable variation in the human genome, and to develop robust strategies for identifying the genetic contribution to diseases and drug responses. Haplotypes of single nucleotide polymorphisms (SNPs) have been suggested as an effective representation of human variation, and various haplotype-based association...

Journal: :Genome research 2013
Wei Chen Bingshan Li Zhen Zeng Serena Sanna Carlo Sidore Fabio Busonero Hyun Min Kang Yun Li Gonçalo R Abecasis

Emerging sequencing technologies allow common and rare variants to be systematically assayed across the human genome in many individuals. In order to improve variant detection and genotype calling, raw sequence data are typically examined across many individuals. Here, we describe a method for genotype calling in settings where sequence data are available for unrelated individuals and parent-of...

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