Searching journal content for articles similar to McClatchy et al. 17 (9): 1378.

Displaying results 1-10 of 3115
For checked items
  1. ...of nematodes is believed to date back to ∼650–750 million years, generating a large and phylogenetically diverse group to be explored. However, for most species high-quality gene annotations are incomprehensive or missing. Combining short-read RNA sequencing with mass spectrometry–based proteomics and machine...
  2. ...different cell and muscle fiber types. Here, we optimize single-nucleus ATAC-seq (snATAC-seq) to map skeletal muscle cell–specific chromatin accessibility landscapes in frozen human and rat samples, and single-nucleus RNA-seq (snRNA-seq) to map cell-specific transcriptomes in human. We additionally perform...
  3. ..., Illinois 60628, USA ↵3 These authors contributed equally to this work. Corresponding author: zhe.ji@northwestern.eduAbstractWe describe a low-input RNase footprinting approach for the rapid quantification of ribosome-protected fragments with as few as 1000 cultured cells. The assay uses a simplified...
  4. ...relies on sequence information to infer evolutionary relationships between genes or proteins. In contrast, protein structural information has long been overlooked, although structures are more conserved and closely linked to the functions than the sequences. To address this gap, we conducted a proteome...
  5. ...Construction and evaluation of a new rat reference assembly, GRCr8, from long reads and long-range scaffolding Kai Li1, Melissa L. Smith2, J. Chris Blazier3, Kelli J. Kochan3, Jonathan M.D. Wood4, Kerstin Howe4, Anne E. Kwitek5, Melinda R. Dwinell5, Hao Chen6, Julia L. Ciosek1, Patrick Masterson7...
  6. ...detection of amino acid substitutions in proteomes reveals mechanistic basis of ribosome errors and selection for translation fidelity. Mol Cell 75: 427–441.e5. doi:10.1016/j.molcel.2019.06.041 ↵Patro R, Duggal G, Love MI, Irizarry RA, Kingsford C. 2017. Salmon provides fast and bias-aware quantification...
  7. ...behavior of RNA andprotein during embryogenesis. We observed a temporal proteome delay in clusters 5 and 6: while the RNA expression peaks around 7 h, proteins steadily up-regulate later in embryogenesis, putatively due to translational control mechanisms (Fig. 7C). Quantification of protein isoforms...
  8. ...-read-based quantification algorithms. By comparing our iso-transcriptome with public proteomics databases, we find that alternative isoforms are elusive to proteogenomics detection. SQANTI allows the user to maximize the analytical outcome of long-read technologies by providing the tools to deliver quality...
  9. ...to characterize sample-specific APA using the corresponding RNA-seq data, but suffered from high error rate on both polyadenylation site (PAS) identification and quantification of PAS usage (PAU), and bias toward 3′ untranslated regions. Here we developed a tool for APA identification and quantification (APAIQ...
  10. ...embryonic transcriptome clusters. RBP candidate cluster enrichment was calculated in two steps using Fisher's exact testing. Since the mass spectrometry protein quantification showed enrichment of higher-expressed genes, we first calculated cluster enrichment for the early embryo proteome and used...
For checked items

Preprint Server