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10.1016/j.tig.2016.05.002

http://scihub22266oqcxt.onion/10.1016/j.tig.2016.05.002
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suck abstract from ncbi


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pmid27220646
      Trends+Genet 2016 ; 32 (7 ): 392-394
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  • Fishing for Function in the Human Gene Pool #MMPMID27220646
  • Barozzi I ; Visel A ; Dickel DE
  • Trends Genet 2016[Jul]; 32 (7 ): 392-394 PMID27220646 show ga
  • Identification and characterization of causal non-coding variants in human genomes is challenging and requires substantial experimental resources. A new study by Tehranchi et al. describes a cost-effective approach for accurate mapping of molecular quantitative trait loci (QTLs) from pooled samples, a powerful way to link disease-associated changes to molecular functions.
  • |*Genome, Human [MESH]
  • |Chromosome Mapping [MESH]
  • |Gene Pool [MESH]
  • |Genetic Diseases, Inborn/*genetics [MESH]
  • |Genetic Variation [MESH]
  • |Humans [MESH]
  • |Polymorphism, Single Nucleotide/genetics [MESH]
  • |Quantitative Trait Loci/*genetics [MESH]


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