Searching journal content for articles similar to Bertone et al. 16 (2): 271.

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  1. ...(Coster et al. 2021). The choice of either analysis approach often impacts the experimental design itself (Harvey et al. 2023). Other factors influencing this decision include computational resources, DNA quality and quantity, sequencing depth, and the ability of assembly-based approaches to improve...
  2. ...For the Daicel Arbor “myBaits Expert Human Affinities” reagent, the oligonucleotide bait design is proprietary, and we do not have access to the technical details. Several modules are available (https://arborbiosci.com/genomics...
  3. ...with high-density DNA oligonucleotide arrays, offers an optimal solution by providing both SNP genotype information as well as CNV profiling in a single experiment. Methods Experiments 500K EA Arrays and the Whole-Genome Sampling Assay (WGSA) The 500K EA arrays contain 534,500 SNPs on two enzyme...
  4. ...al. ( 2004 ) Global identification of human transcribed sequences with tiling arrays . Science 306 : 2242 – 2246 . ↵ Bertone, P. , Trifonov, V. , Rozowsky, J.S. , Schubert, F. , Emanuelsson, O. , Karro, J. , Kao, M.-Y. , Snyder, M. , Gerstein, M. ( 2006 ) Design optimization methods for genomic DNA...
  5. ...respective methylation context (Fig. 1A). The Figure 1. Genomic profiles of DNA methylation of Brachypodium distachyon. (A) Total number of 100-bp genomic tiles (dark gray) are compared to the number of genomic tiles with sequence coverage for all threemethylation sequence contexts. Coverage bar is split...
  6. .... Molecular Inversion Probes (MIPs) In the process of implementing an MIP-based genomic enrichmentmethod,we found that our sequence data included the probe arm sequences that were designed to hybridize to DNA flanking the region of interest (ROI) (data not shown). This occurred when probes were required...
  7. ...relatively modest: to directly compare methods using the same DNA samples and the same arrays. However, we found significant limitations generally to hybridization-based methylation analysis that could largely be overcome with novel statistical procedures and array design algorithms. As will be described...
  8. ...initiation points and can range from the smallest possible distance of one single base up to the length of the probe, or even further. At the design stage it is important to minimize potential cross-hybridization, self-pairing, and other probe sequence artifacts such as DNA secondary structure formation...
  9. ...Genome-wide Detection of Allelic Imbalance Using Human SNPs and High-density DNA Arrays Rui Mei 1 , 7 , Patricia C. Galipeau 2 , Cynthia Prass 3 , Anthony Berno 1 , Ghassan Ghandour 4 , Nila Patil 1 , Roger K. Wolff 3...
  10. ...-tagged cDNAs were expressed in cells transfected on cell arrays (green). Image acquisition is designed in such a way that each image contains only one cell. From top left to bottom right : GFP-tagged NES→cytoplasm (96 images), EGFP→cyto-nuclear (170 images), GFP-tagged cDNA #488→mitochondria (108 images...
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