Searching journal content for articles similar to Lipovich and King 16 (1): 45.

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  1. ...the quantitative levels of gene expression have made significant advances. Large-scale quantitative expression technologies involve the generation of short sequence tags from a given RNA sample, and use the abundance of these sequence tags to determine the relative abundance of each transcript. These methods...
  2. ...was tested by cDNA sequencing with inverse PCR. Surprisingly, 44% of the validated predictions in “intronic” regions revealed a transcript independent of the surrounding gene, and 40% of the validated predictions in “intergenic” regions were part of existing genes. See Fig. 3 for examples. Results...
  3. ..., including RNA editing of mitochondrial transcripts (Shapiro and Englund 1995), polycistronic transcription of nuclear genes (Borst 1986; Tschudi and Ullu 1988), and segregation of chromosomes via an unconventional kinetochore apparatus comprising components distinct from other eukaryotic groups (Akiyoshi...
  4. ...-seq and ATAC-seq profiles around the heat shock protein GrpE2 gene. (G) KAS-seq and ATAC-seq profiles around the LuxR2 transcriptional activator gene. (H) KAS-seq and ATAC-seq profiles near the origin of replication of the Bacteriovorax chromosome.Examination of local browser tracks (Fig. 3B,C) revealed...
  5. ...of unconventional functional features such as fusion transcripts is a challenging task in the effort to annotate all functional DNA elements in the human genome. Paired-End diTag (PET) analysis possesses a unique capability to accurately and efficiently characterize the two ends of DNA fragments, which may have...
  6. ...rectangle) with an untemplated guanine (underlined G), and was followed by a long, pure 3′ poly(A) tract. The transduction indicated a putative donor L1 intronic to the PRDM4 gene on Chromosome 11 (L1RSPRDM4).Using the TEBreak computational pipeline (Carreira et al. 2016), we identified 194 L1, 3348 Alu...
  7. ...out by complete sequencing analysis. Alternatively, the large size of DNA fragments can be analyzed by single-end sequencing or paired-end sequencing. EST was the first tag-based approach, generating one tag per sequencing read, to represent full-length transcripts of expressed genes. The original...
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  8. ...into 171,144 groups, from which 60,770 clones were fully sequenced cDNAs annotated in the FANTOM-2 annotation. We have also produced 547,149 5′ end reads,which clustered into 124,258 groups. Altogether, these cDNAs were further grouped in 70,000 transcriptional units (TU),which represent the best...
  9. ...the fusion junction. Among these predicted chimeras, 44% have more than one genomic sequencing read supporting the same gene pair (Supplemental Fig. 6), suggesting that they may result from genomic-level SVs, rather than read-through at the transcript level. Among the SVs supported by both genomic...
  10. ...and Group II C. botulinum ), a prophage (Group III C. botulinum ), or a plasmid (Group IV C. botulinum ). In Group I (proteolytic) C. botulinum strain Hall A (ATCC 3502), they are organized in two divergent transcriptional units on the chromosome, cntAB and cntCDE , which bracket the regulatory gene, cnt...
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