Searching journal content for articles similar to Nielsen et al. 15 (11): 1566.

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  1. ...-Sánchez E, Sousa VC, Foll M. 2013. Robust demographic inference from genomic and SNP data. PLoS Genet 9: e1003905. doi:10.1371/journal.pgen.1003905 ↵Fraïsse C, Sachdeva H. 2021. The rates of introgression and barriers to genetic exchange between hybridizing species: sex chromosomes vs autosomes. Genetics...
  2. ...are not directly applicable to genotyping studies, which type a pre-ascertained set of SNPs. Given the huge genotyping data sets now available for humans ( Hinds et al. 2005 ; International HapMap Consortium 2005 ), as well as increasingly for other organisms, it will be of interest to assess the reliability...
  3. ...-rumped and fat-tailed sheep breeds. (C) Genome-wide selection sweep tests (the FST-based and π-ratio-based methods) for the tail configuration between fat-rumped and fat-tailed sheep breeds. (D) Calculation of Tajima's D-values and π and FST values for SNPs in the candidate genomic region Chr 8: 87.56–87.88 Mb...
  4. ...encodes the epidermal patterning factor 1 (PpEPF1) involved in stomatal development (Hara et al. 2009), showed strong selection signals, based on the high Tajima's D and μ values (Fig. 5K,L). By scanning the variants in PpEPF1, we found that SNPs with functional significance were absent. Through further...
  5. ..., Bustamante CD. 2005. Genomic scans for selective sweeps using SNP data. Genome Res 15: 1566–1575. Nielsen R, Hubisz MJ, Hellmann I, Torgerson D, Andres AM, Albrechtsen A, Gutenkunst R, Adams MD, Cargill M, Boyko A, et al. 2009. Darwinian and demographic forces affecting human protein coding genes. Genome Res...
  6. ...) and CB4856 (Hawaii), which is suitable for studying -to-phenome relations (Li et al. 2006; Andersen et al. 2012; Sterken et al. 2015). The segregating population consists of 199 homozygous recombinant inbred lines (RILs) that have been SNP genotyped and phenotyped for several traits, including gene...
  7. ...were included in this study. We selected nine species from six islands from the Galápagos archipelago and one from Cocos Island and designed 12 species pairs based on the ranges of sympatry and allopatry and their beak haplogroups (Tables 1, 2). About 7 million SNPs were retained in each species pair...
  8. ...to limit sharing of the DNA. Whole- resequencing was performed with Illumina paired-end sequencing technology, using a HiSeq 2000 instrument at the SNP&Seq Technology Platform of Uppsala University. Individually tagged libraries with insert sizes of ∼450 Evolution of differentiation Genome Research 1661...
  9. ...functional regions does not appear to be substantially different than the genomic background, nor are these regions enriched for alleles that segregate among populations (Hernandez et al. 2011). These observations suggest that classic selective sweeps for adaptive alleles may not be frequent in human...
  10. ...affected by recent selective sweeps. For example, several studies (e.g., Carlson et al. 2005; Williamson et al. 2007; Nielsen et al. 2009) have used the distribution of human SNP frequencies along chromosomes to scan for completed sweeps. Whole- sequence polymorphism data should includemany rare SNPs...
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