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  1. ...: 554 -571. ↵ Wu, J.Q., Shteynberg, D., Arumugam, M., Gibbs, R.A., and Brent, M.R. 2004 . Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing. Genome Res. 14 : 665 -671. Web site references ↵ http...
  2. ...human genes and their simultaneously predicted rat orthologs. The gels contain the RT-PCR sequenced products from human ( A ) and rat ( B ). Each column in the gel contains the sequenced product for one intron tested, with the same columns in the human and rat gels containing products from orthologous...
  3. .... ↵ Wu, J.Q., Shteynberg, D., Arumugam, M., Gibbs, R.A., and Brent, M.R. 2004 . Identification of rat genes by TWINSCAN gene prediction, RT–PCR, and direct sequencing. Genome Res. 14 : 665 -671. WEB SITE REFERENCES ↵ http://www.ncbi.nlm.nih.gov/Traces/ ; NCBI Trace Archive. http://genes...
  4. ...data suggest some genes or exons are missing altogether from the current WormBase predictions ( Merrihew et al. 2008 ). To remedy this situation, one of us (P. Green) has for several years undertaken a directed approach utilizing RT-PCR and RACE to test the remaining unconfirmed splice junctions...
  5. ...by TWINSCAN gene prediction, RT-PCR, and direct sequencing . Genome Res. 14 : 665 – 671 . A tale of two templates: Automatically resolving double traces has many applications, including efficient PCR-based elucidation of alternative splices Aaron E. Tenney 1 , 4 , Jia Qian Wu 2 , 4 , Laura Langton 1 , Paul...
  6. ...) project, to identify human genes not yet in the gene catalogs. Our approach was to produce gene predictions by algorithms that rely on comparative sequence data but do not require direct cDNA evidence, then to test predicted novel genes by RT–PCR. We have identified 734 novel gene fragments (NGFs...
  7. ...for this application. For full ORF gene verification using RT-PCR followed by direct sequencing, it is desirable to place one primer in an exonic region upstream of the start codon. If the primer anneals too close to the start codon, then the region of high-quality sequencing trace may begin after the start codon...
  8. ...by sequencing of the amplicons. To amplify cDNAs, we need reasonably accurate, though not necessarily perfect, gene predictions to use for PCR primer design. The further a prediction is from a true gene structure, the greater the likelihood that PCR primers designed for it will fail. Each failure increases...
  9. ...), the corresponding genes are considered as being putative orthologs. The calculated orthologous relationships for ST7 human, cow, mouse, and rat gene sequences are shown in Figure 3 . For these four species, all six pairwise transcript sequence comparisons identified the ST7 gene as the reciprocal best match...
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