Searching journal content for articles similar to Haelterman et al. 24 (10): 1707.

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  1. ...-derived sequences (Lipatov et al. 2005). A recent transcriptome-wide study identified 327 genes in Drosophila melanogaster that generate chimeric transcripts across different populations (Oliveira et al. 2023). Among all genes, 76 generate chimeric transcripts from TE insertions that were present in one strain...
  2. ...identified in a West African and a European population of Drosophila melanogaster, and a European population of Drosophila simulans. (A) The genomic positions of the SNMs on chromosomes. Each gray bar represents the of one offspring. Point color represents mutation type and point shape represents...
  3. ...(Supplemental Table S1), similar to what has been found in earlier studies of Drosophila melanogaster and Caenorhabditis elegans (Lipinski et al. 2011; Schrider et al. 2013). Overall, partial gene CNVs exhibited the same general patterns as complete gene CNVs, with significantly higher rates in NiCu lines (Mann...
  4. ...-induced misincorporation tRNA sequencing), an RNA-seq pipeline designed for tRNA analysis (Behrens et al. 2021), in our study of tsRNAs in Drosophila melanogaster. The library construction step of this pipeline includes necessary measures to minimize tRNA modifications that can hinder effective detection and quantitation...
  5. ...than insertions when repeated sequences were excluded. Because deletions also tended to be longer, mutations have the tendency to reduce size. Similar patterns in mutational bias have been observed for Drosophila melanogaster (Leushkin et al. 2013). For repeated sequences, we analyzed homopolymer...
  6. ...Genome-wide chemical mutagenesis screens allow unbiased saturation of the cancer and identification of drug resistance mutations Jonathan S. Brammeld,1 Mia Petljak,1 Inigo Martincorena,1 Steven P. Williams,1 Luz Garcia Alonso,2 Alba Dalmases,3 Beatriz Bellosillo,3 Carla Daniela Robles-Espinoza,4...
  7. .... Identification of EMS-induced mutations in Drosophila melanogaster by whole- sequencing. Genetics 182: 25–32. Bowen ME, Henke K, Siegfried KR, Warman ML, Harris MP. 2012. Efficient mapping and cloning of mutations in zebrafish by low coverage whole sequencing. Genetics 190: 1017–1024. Brenner S. 1974...
  8. ...Mapping the pericentric heterochromatin by comparative genomic hybridization analysis and chromosome deletions in Drosophila melanogaster Bing He 1 , Amy Caudy 2 , Lance Parsons 2 , Adam Rosebrock 3 , Attilio Pane 1 , Sandeep Raj 1...
  9. ..., and turn to the study of the Trichoplax or Loxodonta s. There remains much to discover, and many resources are now available to catalyze discovery by individual research groups ( Matthews et al. 2005 ), who will remain the bedrock of the Drosophila community in the post-genomic era ( Gilbert 1991 ). Large-scale...
  10. ...in Drosophila melanogaster rely on a chromosome carrying multiple dominant or recessive marker mutations with visible phenotypes. These visible phenotypes are often laborious to score and may interfere with the phenotype of the mutant of interest. Most importantly, because mutations with easily scored, viable...
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