Searching journal content for articles similar to Elvers et al. 25 (11): 1634.

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  1. ...Accelerated somatic mutation calling for whole- and whole-exome sequencing data from heterogenous tumor samples Shuangxi Ji1, Tong Zhu2, Ankit Sethia2 and Wenyi Wang1 1Department of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030...
  2. ...Kohei Hagiwara, Andrew Thrasher, Nadezhda V. Terekhanova, and Jinghui Zhang Department of Computational Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee 38105, USA Allele-specific expression (ASE) of somatic mutations can be caused by cis-activation of the mutant allele...
  3. ...adjacent to the tumor does not reflect a normal genomic state and has undergone an accumulation of low-frequency somatic mutations.Somatic SVs are prominent in adjacent nontumor tissuesA recent study revealed that cirrhotic livers exhibit a higher mutation burden compared to normal livers, with the most...
  4. ...and transcriptomic levels, along with their regulatory effects on structural variations (SVs) and gene expression. Functional validation is performed using dual-luciferase assays and cell-based experiments. Our findings reveal that integrated HBV sequences form long concatemers, mediating inter- and intrachromosomal...
  5. ...basenji dog (Canis lupus familiaris) . BMC Genomics 22: 188. doi:10.1186/s12864-021-07493-6 ↵Elvers I, Turner-Maier J, Swofford R, Koltookian M, Johnson J, Stewart C, Zhang CZ, Schumacher SE, Beroukhim R, Rosenberg M, et al. 2015. Exome sequencing of lymphomas from three dog breeds reveals somatic...
  6. ...-in sequences reveals 16 major clusters among the 65,536 spike-ins. (D,E) Visualization of all spike-in RNAs, color-coded by GC-content cluster and by MFE cluster. The nine GC-content categories and 120 MFE levels reflect the full breadth of the 65,536 spike-in sequences.For validation, we designed synthetic...
  7. ...a comprehensive APA atlas for 261 cell types across 19 porcine tissues based on single-nucleus RNA sequencing (snRNA-seq) data. This analysis reveals tissue- and cell type–specific patterns of APA. We find that many genes display a clear correlation between the average length of 3′ untranslated regions (3′ UTRs...
  8. ...estimates place the average timing of introgression between 6100 and 3000 years ago, with low sequence divergence to dogs from the Iberian Peninsula suggesting a single local origin for the hybridization event. Using forward genetic simulations, we show that the introgressed haplotype is most likely being...
  9. ..., Feusier J, Gupta M, Nicholas TJ, Brown J, Baird L, et al. 2021a. De novo structural mutation rates and gamete-of-origin biases revealed through sequencing of 2,396 families. Am J Hum Genet 108: 597–607. doi:10.1016/j.ajhg.2021.02.012 ↵Belyeu JR, Chowdhury M, Brown J, Pedersen BS, Cormier MJ, Quinlan AR...
  10. ...al. 2022; Kong et al. 2023). Many sequencing-based approaches, using short- or long-read sequencing platforms, map RNA modifications across the transcriptome, revealing their patterns in normal and disease states across various cell types, tissues, organisms, and under different environmental...
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