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  1. ..., respectively. nFuse does not estimate copy count and therefore could not be compared. Overall, this shows that CouGaR generates reliable predictions of genomic rearrangements. Figure 2. Analysis of DIPG29. (A) The predicted CGRs are convolved into a unique structure as visualized by CouGaR-Viz (the four...
  2. ...programming algorithm to assign repetitive reads that minimizes differences of WGS data sets, RNA-seq data sets, and the reference . nFuse (McPherson et al. 2012) is a computational tool intended to identify complex genomic rearrangements from whole- data with the help of transcriptome sequencing data. More...
  3. ...-level using Pacific Biosciences (PacBio) HiFi long reads and high-throughput chromosome conformation capture (Hi-C) scaffolding (Wood et al. 2023; Bishop et al. 2023a,b, 2024).View larger version: In this window In a new window Figure 1. Comparative genomics of five chromosome-scale bryozoan s. (A...
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