Searching journal content for articles similar to Frisch et al. 12 (2): 349.

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  1. ...chromosome scaffolds. J. Cell. Biol. 100 : 1706 -1715. ↵ Frisch, M., Frech, K., Klingenhoff, A., Cartharius, K., Liebich, I., and Werner, T. 2002 . In silico prediction of scaffold/matrix attachment regions in large genomic sequences. Genome Res. 12 : 349 -354. ↵ Galande, S. and Kohwi-Shigematsu, T. 1999...
  2. ...cluster varied greatly for the different properties, which again indicates that the different properties contain complementary information. Bode et al. (2006) have shown that it is very hard to identify scaffold/matrix attachment regions (SMARs) from the sequence, as the important scaffold proteins...
  3. ...: 155 – 161 . ↵ Heng, H.H. , Goetze, S. , Ye, C.J. , Liu, G. , Stevens, J.B. , Bremer, S.W. , Wykes, S.M. , Bode, J. , Krawetz, S.A. ( 2004 ) Chromatin loops are selectively anchored using scaffold/matrix-attachment regions . J. Cell Sci. 117 : 999 – 1008 . ↵ Horton, R. , Wilming, L. , Rand, V...
  4. ...in silico is challenging; researchers often analyze an arbitrary sequence length surrounding the TSS or rely on database-mined experimental data. Sequence conservation analysis can help identify important regulatory sequences (Stark et al. 2007).At least 40%–50% of human genes are subject to some degree...
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  5. ...homology and in silico structural prediction. The first gene encodes a tyrosine recombinase/integrase that likely recognizes and cuts at the AATTAACTTAT motif in the and in the circularized version (resulting in Yucahu-i linearization) and may be involved in integration of the linear sequence...
  6. ...) is used to model common latent factors across multiple omics layers (Argelaguet et al. 2018). Unified nonnegative matrix factorization (UNMF) focuses on decomposing nonnegative matrices into interpretable, lower-dimensional components that capture the underlying structure and patterns within individual...
  7. ...the OM assembly to perform hybrid scaffolding on both the SR and LR assemblies. First, the sequence assembly contigs or scaffolds were converted into sequence maps by running an “in silico digestion” based on the known Nt.BspQI recognition motif using the IrysView software (BioNano Genomics). Then...
  8. ...subclade retrotransposons uncovered by our pipeline specialize at chromosome ends in their respective host species. Testing this prediction first requires molecular biology to confirm that (1) these in silico–generated consensus sequences represent actual elements in the targeted s and (2) the elements...
  9. ...and not closely related to each other (less than five SNP distance).Assembly and annotationGenome assembly, scaffolding, and gap-closing of the Illumina sequence reads obtained in this study and from public databases were performed using the Platanus assembler (Kajitani et al. 2014). Original assemblies were used...
  10. ...with available genomic scaffolds. In brief, we extracted CEN180 variants from all available A. thaliana genomic sequences, partitioned the variants into clusters with shared segregating sites, and then probed for sequence fingerprints of each cluster in CENH3 ChIP-seq data sets. The fact that experimental FISH...
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