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  1. ...for the speciation and adaptations such as mimicry (Joron et al. 2011; Hill et al. 2019; de Vos et al. 2020), mostly owing to reciprocal translocation and repeated events of fusion and fission among a highly dynamic number of chromosomes between species.To better understand the phenomenon of scrambling, we study...
  2. .... By aligning the sequencing data of L. oculatus and A. spatula to Chromosome 3 of A. spatula, we found that, at the fusion region, the sequencing depth of a 2-kb fragment in L. oculatus was zero, whereas A. spatula showed a relatively high sequencing depth in the fusion region. Further genomic feature analysis...
  3. ...exceptions. By combining short and long reads in CTAT-LR-Fusion, we are able to further maximize the detection of fusion splicing isoforms and fusion-expressing tumor cells.Genomic rearrangements involving chromosomal translocations or deletions can yield fusion genes, in some cases activating oncogenes...
  4. ...-ChIP, RHΔ is expressed in vivo with an epitope tag, and genomic sequences bound by RHΔ are recovered via chromatin immunoprecipitation. (F) MapR uses a purified RHΔ–MNase fusion protein to bind and cleave chromatin fragments containing R-loops, which are then purified and sequenced.To provide an orthogonal...
  5. ...fusions or fissions. Also, the comparison of T. panzhihuanense with the long-read-based high-quality Morchella sextelata M. Kuo assembly revealed relatively high levels of mesosynteny conservation between the two species (Fig. 5B; Supplemental Fig. S14B). Indeed, 61% of the T. panzhihuanense and 70...
  6. ...in the three-dimensional (3D) chromatin structure in turtles compared to other amniotes beyond the fusion/fission events detected in the linear s. Namely, whole- comparisons revealed distinct trends of chromosome rearrangements in turtles: (1) a low rate of reshuffling in Apalone (Trionychidae) whose karyotype...
  7. ...José Carlos Montañés1, Marta Huertas1, Simone G. Moro1, William R. Blevins1,4, Mercè Carmona2, José Ayté2, Elena Hidalgo2 and M. Mar Albà1,3 1Evolutionary Genomics Group, Research Program on Biomedical Informatics, Hospital del Mar Medical Research Institute (IMIM) and Universitat Pompeu Fabra (UPF...
  8. ...: chirag@iisc.ac.inAbstractAffordable genotyping methods are essential in genomics. Commonly used genotyping methods primarily support single-nucleotide variants and short indels but neglect structural variants. Additionally, accuracy of read alignments to a reference is unreliable in highly polymorphic...
  9. ...or His N-terminal fusion proteins or untagged proteins were used for the pulldown. Pulldown specificity was validated using glutathione agarose (GST) or nickel-IMAC agarose (Ni2 + NTA) beads. Unspecific binding or cross-reactivity of tagged proteins in the IP fraction of the pulldowns was not observed...
  10. ...of macrochromosome ends (e.g., with higher GC content) is thought to be a remnant of the fusion of one or more microchromosome(s) to a macrochromosome (Waters et al. 2021). This hypothesis is not supported by our observation that even species possessing no explicit microchromosomes (e.g., western clawed frog) have...
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