Searching journal content for articles similar to Haussmann et al. 34 (12): 2279.

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  1. ...of generating a knockout allele. We redesigned the mutagenesis strategy and tested an alternative 3′ CRISPR-Cas9 sgRNA (sgRNA-F), which binds within exon 8 with an aim of increasing the likelihood of mutagenesis (Supplemental Fig. S1). This sgRNA showed a high rate of mutagenesis in vitro, as assessed by a high...
  2. ...Corrigendum: Cre-dependent Cas9-expressing pigs enable efficient in vivo editing Kepin Wang, Qin Jin, Degong Ruan, Yi Yang, Qishuai Liu, Han Wu, Zhiwei Zhou, Zhen Ouyang, Zhaoming Liu, Yu Zhao, Bentian Zhao, Quanjun Zhang, Jiangyun Peng, Chengdan Lai, Nana Fan, Yanhui Liang, Ting Lan, Nan Li...
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  3. ...regulation, and cell differentiation. Nevertheless, StripeDiff does not provide a user-friendly package to directly call all stripes with common contact map files.Here we introduce Quagga, a statistically rigorous, algorithmically efficient, and interpretable tool to identify stripes. Quagga's biggest...
  4. ..., UCell, and JASMINE—across nine healthy and cancer scRNA-seq data sets demonstrates their insufficiency in fulfilling this requirement. To address this limitation, we present Adjusted Neighborhood Scoring (ANS), a deterministic algorithm with enhanced control gene selection that significantly improves...
  5. ...be an unreliable indicator of sgRNA efficiency in H9 hESCs owing to the limited sensitivity of this analysis (Fig. 2D).Notably, the CRISPR-Cas9 targets in the proximity group had significantly lower Hi-C scores in hESCs compared to in K562 cells (P = 0.004) (Supplemental Fig. S13), possibly suggesting...
  6. ...is increasing rapidly. Accurate inference of cell lineage tree from large single-cell data is computationally challenging. In this paper, we present ScisTree2, a fast and accurate cell lineage tree inference and genotype calling approach based on the infinite-sites model. ScisTree2 relies on an efficient local...
  7. ...or subtle spatial patterns, and they frequently fail to scale efficiently with large data sets. Here, we introduce geneCover, a label-free combinatorial method that selects an optimal panel of minimally redundant marker genes based on gene-gene correlations. Our method demonstrates excellent scalability...
  8. ...observed in the 10x Visium data set. This trend continued in the Stereo-seq data set, confirming successful integration across donors. Additionally, we evaluated computational efficiency. stMSA processed up to 20 slices with <12 GB of GPU memory, whereas Stitch3D, SPACEL, and SEDR struggled to handle...
  9. .... To this end, we present a cross–data set cell type annotation methodology with a universal reference data and method selection strategy (CAMUS) to achieve highly accurate and efficient annotations. We demonstrate the advantages of CAMUS by conducting comprehensive analyses on 672 pairs of cross-species sc...
  10. ...-based screens.View this table: In this window In a new window Table 1. A collection of CRISPR screening data sets used in the studyResultsSelection of the efficient and inefficient sgRNAs in CRISPR/Cas9 knockout screensTo construct a predictive model, we took two steps to identify efficient and inefficient sgRNAs...
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