AGOG
发表于 2025-3-28 17:19:12
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咯咯笑
发表于 2025-3-28 18:44:26
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漫不经心
发表于 2025-3-28 23:06:43
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Credence
发表于 2025-3-29 05:29:13
Functional Annotation of Rare Genetic Variants,diseases and phenotypes. In the majority of cases though, the variants are predicted to have small to modest effect sizes, and, due to the technologies used, many of the signals discovered so far may not be the causal loci. As rare variation studies begin to explore the lower ranges of the allele fr
COUCH
发表于 2025-3-29 09:26:58
The 1000 Genomes Project,rize genomic differences between individuals in a systematic fashion. Multiple studies were initiated with the aim of investigating human genetic variation (Pennisi 2007), most prominently the Human Genome Diversity Project (Jakobsson et al. 2008; Li et al. 2008; Cavalli-Sforza 2005) and the Interna
evasive
发表于 2025-3-29 13:46:15
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新手
发表于 2025-3-29 17:54:24
Population Isolates,sible for rare recessive diseases, and recently to assess complex traits and common diseases, with particular emphasis on detecting founder causative variants. The existence of large data sets, well-ascertained pedigrees, and detailed clinical records are only a subset of the features that make cond
alcoholism
发表于 2025-3-29 20:02:46
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性上瘾
发表于 2025-3-30 03:57:04
Collapsing Approaches for the Association Analysis of Rare Variants,quency. Collapsing approaches overcome this power loss by testing for an association with an aggregate of rare variants. These tests pool information across the rare variants such that a single test is performed on the summary statistic, and are powerful tools, provided that certain conditions are s
Fecundity
发表于 2025-3-30 07:42:03
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