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  1. ...-seq supports the bulk of transcripts detectable in embryogenesis, improves preFigure 1. Mapping of transcription initiation in zebrafish embryo development. (A–C ) Genome browser view of ncalda gene with CAGE-seq, ChIP-seq, and RNA-seq tracks from selected developmental stages. Schematic representation...
  2. ...% of zebrafish genes. Comparison of the patterns of 39 end usage in different stages revealed several significant trends, such as the usage of shorter 39 UTRs in the ovaries, preferential depletion of short 39 UTRs in the early embryo, and widespread polyadenylation at noncanonical sites, which appears to occur...
  3. ...). Based on integrative analysis of EST, SAGE, and microarray data, tandem 39 UTR lengthening has been observed during mouse embryogenesis ( Ji et al. 2009). However, the specific genes directly regulated by APA during vertebrate development remain unknown. Several high-throughput sequencing methods have...
  4. .... , Eun A. , He Y. , Ma W. , Wang W. , Wen Z. , et al. ( 2003 ) 15000 unique zebrafish EST clusters and their future use in microarray for profiling gene expression patterns during embryogenesis. Genome Res. 13 : 455 – 466 . ↵ Moriyama E.N. , Powell F.R. ( 1996 ) Intraspecific nuclear DNA variation...
  5. ...this potential variability, we show many of the Iso-Seq TSSs were accurate, confirmed by patterns of accessible chromatin from ATAC-seq. Correct TSSs/TTSs are particularly important for future work in threespine stickleback fish in understanding gene regulation. Additional work mapping accessible chromatin...
  6. ...found that 24% of them (or 36 genes) are also activated prior to themidblastula transition in zebrafish (Aanes et al. 2011). The list of 150 genes, together with their expression profiles and associated GO terms, are provided in Supplemental File S4. We used quantitative real-time PCR (RT...
  7. ...is now available, in the form of ESTs in both X. laevis and X. tropicalis , as well as sequence information in the case of X. tropicalis . Therefore, in the next phase of screens, it would seem prudent to use a unique set of genes, rather than randomly selected clones for the screen. The Ueno group...
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  8. ...the author’s laboratory) to establish a comprehensive EST database via analysis of mRNAs from a broad range of opossum tissues and life stages that can be used to seek novel opossum transcripts, augment and refine the current annotation, and guide the design of basic gene-expression microarrays for -wide...
  9. ...if expression profiles were available on all the ESTs. “The joy of screening” will come not only from finding new interesting phenotypes, but from the knowledge that the genes responsible for these phenotypes have been isolated already. Acknowledgments We thank members of our laboratories and many colleagues...
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