Searching journal content for articles similar to Zhang et al. 35 (12): 2781.

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  1. ...tools enables high-fidelity, large-scale profiling of microsatellites, which may find utility in diverse applications such as lineage tracing, population genetics, ecology, and forensics.Microsatellites, also known as short tandem repeats, are genomic sequences composed of tandem repeats of short (1...
  2. ...-Relate on the UK Biobank and All of Us data sets. On a data set of 200,000 individuals split between two parties, SF-Relate detects 97% of third-degree or closer relatives within 15 h of runtime. Our work enables secure identification of relatives across large-scale genomic data sets.Collaborative studies that aim...
  3. ...relevant to the target using a k-mer-based greedy heuristic (Sirén et al. 2024).Low-coverage sequencing, combined with genotyping and phasing, is a cost-effective approach to conduct large-scale genetic studies (Davies et al. 2021; Li et al. 2021; Martin et al. 2021; Rubinacci et al. 2021). In this paper...
  4. ...: In this window In a new window Figure 2. Large scale-identification of species-specific orphan genes (SSOGs) in the human gut microbiome. (A) The main steps of the computational workflow of similarity searches. (B) Distribution of the SSOG proportion in a given species’ pan. The red dashed line denotes...
  5. ..., morphology, and disease susceptibility. We explore the limitations of current data sets for variant interpretation, tradeoffs between sequencing strategies, and the burgeoning role of long-read s for capturing structural variants. In addition, we consider how large-scale collections of whole- sequence data...
  6. ...the genomic outcomes of CRI-SPA-Map engineering, we whole- sequenced 185 555 CRI-SPA-Map isolates (typically four local and two distal isolates; Supplemental Table S2) 186 created from the 92 YKO strains. We analyzed genotype calls at 8,257 high-quality variants 187 across the (7,954 SNVs and 303 indels...
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  7. ...a window-based optimization scheme that enables accelerated convergence while improving the accuracy. Additionally, PCAone incorporates out-of-core and multithreaded implementations for the existing Implicitly Restarted Arnoldi Method (IRAM) and RSVD. Through comprehensive evaluations using multiple large-scale...
  8. ...Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets Jeanlin Jourdain,1,2 Harmonie Barasc,3 Thomas Faraut,3 Anne Calgaro,3 Nathalie Bonnet,3 Camille Marcuzzo,4 Amandine Suin,4 Anne Barbat,2 Chris Hozé,1...
  9. ...score ranges. Although other Tirosh-based methods showed high information quantity, they suffered from large-scale imbalances, likely owing to biased control gene selection and lack of score normalization.It is important to emphasize that gene signature scoring is only as reliable as the provided...
  10. ...to the genotype called from the high coverage data. This motivated us to carry out systematic revisions of conflicts between the GT and GP values, which could be characteristic only for ultralow coverage data, and to focus our search for optimal solutions in the GDI design on the combination of INFO score, GP...
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