Searching journal content for articles similar to Melamed et al. 32 (3): 488.

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  1. ...found no evidence for an increased point mutation rate in animals born via in vitro fertilization (IVF) (Caperton et al. 2007), a retrospective comparative analysis in humans uncovered a significantly higher de novo point mutation rate in IVF-born children (Wang et al. 2021). However, the underlying...
  2. ...in postduplication FIE-gene and FIE-functional family diversity, relative to background mutations, compared with preduplication.These observed increases in diversity indicate the selection for gene duplication events, which can broaden the range of possible functional adaptations available to the tumor. Somatic copy...
  3. ...emerged transcription of a pre-existing ORF. (B) De novo gene emergence from a frameshifted gene sequence. (Created with BioRender; https://www.biorender.com/.)Merging comparative genomic and transcriptomic data allow detection of both the lineage-specific transcripts and the mutations responsible...
  4. ...for this deviation from the prediction of the theory may lie in the adaptability offered by a higher mutation rate, as we were able to show that the of the widely studied Hydra magnipapillata strain 105 has undergone a process of strong positive selection since the strain's cultivation 50 years ago. This most likely...
  5. ...1 Title 1 Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals 2 conserved gene alterations linked to Parkinson’s disease 3 Running title: Substantia nigra aging linked to Parkinson 4 Kangli Wang1, Weikun Xia1, Yingli Gu1, Songpeng Zu1, Qian Yang2, Maria Luisa Amaral1...
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  6. ...acid sequences when necessary, and, most importantly, integrate other sequencing data types with single-nucleotide resolution, in which specific nucleotide positions convey sequence read information. Together, ggRibo enables parallel comparisons of multiomic data sets, facilitating the study of gene...
  7. ...Full-resolution HLA and KIR gene annotations for human assemblies Ying Zhou1, Li Song2 and Heng Li1,3 1Department of Data Science, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA; 2Department of Biomedical Data Science, Dartmouth College, Hanover, New Hampshire 03755, USA; 3...
  8. ...and adaptive sampling with a bioinformatic pipeline to produce haplotype-resolved, annotated IGH assemblies. Notably, our strategy overcomes prior limitations in phasing resolution, enabling single-contig haplotype assemblies that span the entire IGH locus. We apply this method to four individuals and validate...
  9. ...in modeling gene expression changes resulting from sequence variants. Yet, few methods operate at the resolution necessary to capture subtle effects of single-nucleotide changes. Furthermore, it remains unclear which architectural components, such as residual connections, normalization strategies...
  10. ...Cell type–specific gene regulatory atlas prioritizes drug targets and repurposable medicines in Alzheimer's disease Yunxiao Ren1,2, Ming Hu3,4, Yang E. Li5, Andrew A. Pieper6,7,8,9,10,11, Jeffrey Cummings12 and Feixiong Cheng1,2,4,13 1Cleveland Clinic Genome Center, Cleveland Clinic Research...
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