Searching journal content for articles similar to Maydan et al. 17 (3): 337.

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  1. ...with the array of tools available for C. elegans, using all three sequencing technologies (Illumina, PacBio, and Nanopore) would be optimal.ResultsGenome sequencing and C. elegans strainWe sought to generate a new C. elegans assembly that matches a modern and easily available reference strain, VC2010 (Flibotte...
  2. .... Their structure has mostly been explored with low-resolution labor- and resource-intensive techniques such as genetic linkage mapping, fluorescence in situ hybridization, PCR analysis (Zhao et al. 2006), SNP mapping (Kadandale et al. 2005), and oligonucleotide array comparative genomic hybridization (Maydan et al...
  3. ...,371 92.7% CNVs Variant class Method Called events Validated events % validated Duplications Array CGH 31 26 84% Deletions Array CGH 15 15 100% C. elegans mutation resource Genome Research 1751 www..org ild ild Thompson et al. 1752 Genome Research www..org the centers (Fig. 2B). This bias was not seen...
  4. ...These authors contributed equally to this work. Corresponding author: elegans@snu.ac.krAbstractLong-read sequencing technologies have contributed greatly to comparative genomics among species and can also be applied to study genomics within a species. In this study, to determine how substantial genomic changes...
  5. ...elegans pathogenesis model. Cell 96: 47–56. Maydan JS, Flibotte S, Edgley ML, Lau J, Selzer RR, Richmond TA, Pofahl NJ, Thomas JH, Moerman DG. 2007. Efficient high-resolution deletion discovery in Caenorhabditis elegans by array comparative hybridization. Genome Res 17: 337–347. McCarroll SA, Murphy CT...
  6. ..., J.L., and Ekker, M. 2003 . Regulatory roles of conserved intergenic domains in vertebrate Dlx bigene clusters. Genome Res. 13 : 533 -543. ↵ GuhaThakurta, D., Schriefer, L.A., Waterston, R.H., and Stormo, G.D. 2004 . Novel transcription regulatory elements in Caenorhabditis elegans muscle genes...
  7. ...oligonucleotide resequencing arrays have allowed the comprehensive discovery of single nucleotide polymorphisms (SNPs) in eukaryotic genomes of moderate to large size. With this technology, the detection rate for isolated SNPs is typically high. However, it is greatly reduced when other polymorphisms are located...
  8. ...of consensus TE sequences (Fig. 3A). Using a false-discovery threshold of q = 0.05, we searched for significant matches between our predicted ZNF binding motifs and TE consensus sequence and then compared them to equivalently sized libraries of nonrepetitive genomic sequence. For all four species, we observed...
  9. ...introns via the detection of accumulated lariats, we isolated total RNA from diploid dbr1/dbr1 and DBR+/DBR+ yeast strains, labeled it as double-stranded cDNA, and hybridized the cDNA to S. cerevisiae tiling arrays. Signals enriched in the dbr1 strain were identified and mapped to genomic coordinates. We...
  10. ...of Colorado at Denver and Health Sciences Center, Aurora, Colorado 80045, USA Abstract Given the evolutionary importance of gene duplication to the emergence of species-specific traits, we have extended the application of cDNA array-based comparative genomic hybridization (aCGH) to survey gene...
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