Searching journal content for articles similar to Mortazavi et al. 20 (12): 1740.

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  1. ...1 assembly. Independently, we predicted 23,249 genomic loci encoding StringTie2 transcripts assembled from ribodepleted RNA-seq data (Wang et al. 2022). These transcripts overlapped with (and thus confirmed) known or predicted N2 or AUGUSTUS protein-coding genes and with known N2 ncRNA genes (Table...
  2. ...-level using Pacific Biosciences (PacBio) HiFi long reads and high-throughput chromosome conformation capture (Hi-C) scaffolding (Wood et al. 2023; Bishop et al. 2023a,b, 2024).View larger version: In this window In a new window Figure 1. Comparative genomics of five chromosome-scale bryozoan s. (A...
  3. ..., experimentally validated annotations are essential. To address this issue, de novo assembled contigs from RNA-seq data of poly(A)-enriched mRNA are useful. As mRNAs are devoid of introns, the resulting predictions are likely more accurate than predicting gene models from genomic sequences that are based...
  4. ...for metazoan repeats) (Chen 2004). We mapped the RNA-seq reads to the repeat-masked using HISAT2 (version 2.2.1; hisat2-build for indexing and hisat2 with default options to map the RNA-seq reads to the corresponding ) (Kim et al. 2019b). RNA-mapping data were used to annotate genes using BRAKER (version 2...
  5. ..., and comparative nematode and epi studies.Genome maintenance and stability are paramount for organisms. Major changes and instability can lead to abnormalities, disease, and lethality. While a variety of cellular processes have evolved to ensure stability, some organisms have developed processes that lead...
  6. ...during post-assembly analysis. Thus, we investigated the coverage of the transcript sequences. Reads from all the RNA-seq data in theOysterGenomeProjectwere assembled into contigs (RNA-contigs) using Trinity (Supplemental Methods; Grabherr et al. 2011).We thenmappedRNA-contigswhose lengths exceeded 500...
  7. ...address questions about microsporidia biology and evolution. We sequenced three microsporidian genomes from two species, Nematocida parisii and Nematocida sp1, which are natural pathogens of Caenorhabditis nematodes and provide model systems for studying microsporidian pathogenesis. We performed...
  8. ...be overlooked in traditional pairwise comparative analyses relying on a single reference per population or species.The nematode species pair Caenorhabditis briggsae and Caenorhabditis nigoni has emerged as a powerful model for dissecting the genetic and genomic bases of speciation. Although both species...
  9. ...nematode Caenorhabditis elegans is ideal to study these interactions because it possesses a well-defined 3′ UTRome. To improve its annotation, we have used a -wide bioinformatics approach to download raw transcriptome data for 1088 transcriptome data sets corresponding to the entire collection of C...
  10. ...of duplicated and de novo genes (Rödelsperger et al. 2019). One major prediction of this rapid turnover model is that the contribution of both categories of origin will depend on the evolutionary distance of the comparison. In this study, we explicitly test this model using genomic data of the nematode...
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