Searching journal content for articles similar to Louie et al. 13 (12): 2594.

Displaying results 1-10 of 2486
For checked items
  1. ...genomic variation. STRs are important to genotype directly, as they cannot always be imputed with single-nucleotide variations (SNVs), but these elements are difficult to resolve with traditional sequencing methods and complex to analyze. They are multiallelic and defined by both their length and motif...
  2. ...and precision medicine (Romero et al. 2016; Montserrat et al. 2020; Dominguez Mantes et al. 2023). Here, we explore the use of variational autoencoders (VAEs), a type of neural network used to learn a low-dimensional representation of the data, to analyze sequences of single nucleotide polymorphisms (SNPs...
  3. ...cohort consists of two litters of half-siblings. Circles represent females and squares represent males. (B) Box plots showing the median, interquartile range, and full range of dnSNV rates per base pair/generation across G2 samples. (C,D) Box plots summarizing sample- and cohort-level variation...
  4. ...and accuracy of SynMall, we perform regular updates across four major resource types: variants, literature, external database annotations, and variant-centered computational tools. Given SynMall already provides all human sSNVs, for non-human species, we aggregate data annually from Ensembl Variation (Hunt et...
  5. ...-cell RNA-seq methods to study the variation of the targets and the microRNAs themselves, and transcriptional inhibition to measure target half-lives. We find that microRNAs form four distinct coexpression groups across single cells. In particular, the mir-290 and the mir-182 clusters are abundantly...
  6. ...al. 2009). More recently, larger variations in TL across natural isolates have been reported (D'Angiolo et al. 2023; O'Donnell et al. 2023). Using short-read whole- sequencing data, D'Angiolo and colleagues (2023) found that wild strains display shorter telomeres than strains from domesticated...
  7. ...-CHM13 reference thus facilitates enhanced discovery of new disease-causing variation, benefiting, for example, rare-disease diagnostics.The first draft of the human reference was published by the Human Genome Sequencing Consortium in 2001 (International Human Genome Sequencing Consortium 2001). Since...
  8. ...and gene conversion (Liao 1999). However, the extent of homogenization and variation in observed copy numbers may vary across tandem arrays and may be shaped by various factors (such as natural selection, drift, mutation, drive, age, size, and relative rates of different kinds of recombination) acting...
  9. ...Genome-wide patterns of selection–drift variation strongly associate with organismal traits across the green plant lineage Kavitha Uthanumallian1, Andrea Del Cortona2, Susana M. Coelho3, Olivier De Clerck2, Sebastian Duchene4,5 and Heroen Verbruggen1,6 1Melbourne Integrative Genomics, School of Bio...
  10. ...Quadrupia provides a comprehensive catalog of G-quadruplexes across s from the tree of life Nikol Chantzi1,11, Akshatha Nayak1,11, Fotis A. Baltoumas2,3,11, Eleni Aplakidou2,3, Shiau Wei Liew4,5, Jesslyn Elvaretta Galuh4,5, Michail Patsakis1, Austin Montgomery1, Camille Moeckel1, Ioannis Mouratidis...
For checked items

Preprint Server