Searching journal content for articles similar to Jeong et al. 29 (6): 999.

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  1. ...information on a target site of interest.The advent of innovative methodologies, such as those integrating CRISPR/Cas systems with RNA-processing approaches, has expedited research in this domain, furnishing novel tools for dissecting the roles of post-transcriptional modifications in gene expression dynamics...
  2. ...2018). miRNAs group into seed families that mostly target the same pool of mRNAs through complementary base pairing of their 7-nt seed region (Lai 2002; Bartel 2009). Each family targets hundreds of mRNAs, and together, miRNAs are considered key post-transcriptional regulators (Friedman et al. 2009).It...
  3. ...collection established with a pooled CRISPR library consisting of 18,414 sgRNAs that target 10,480 genes. Then, we show the editing efficiency and the strong capability of reverse and forward genetic screening of this transgenic collection.ResultssgRNA design and characteristics of the selected target sites...
  4. ...platform and evaluated the correlation between drug sensitivity and LTR7-PLAAT4 status in the organoids. A bespoke 64 compound library was assembled for screening, including chemotherapy (n = 14) and targeted drugs (n = 23) (Supplemental Table S8). As positive controls, one organoid (DAC78) bearing...
  5. ..., CRISPR-Cas9-mediated perturbation, and overexpression screens, to address numerous questions in biology and medicine without relying on a limited number of reporter genes (Adamson et al. 2016; Dixit et al. 2016; Jaitin et al. 2016; Aarts et al. 2017; Datlinger et al. 2017).Here, we introduce i...
  6. ...the for a complementary sequence. When such a target DNA sequence is identified, the enzyme becomes active and can cleave the DNA backbone at that genomic location. The search and recognition mechanism for CRISPR enzymes is highly specific to the spacer sequence of the provided gRNA, but incomplete base pairing between...
  7. ...these benchmarks, FocalSV(target) used regions of interest defined by SVs identified by GIAB. To avoid biased evaluation, we also measured false positive (FP) counts within regions lacking known SVs. Recognizing that some tools may report fewer SVs—leading to lower recall but artificially high precision—we further...
  8. ...identified the exact position of the CTCF and TCF/LEF binding site(s) within these RUW regions and designed CRISPR sgRNAs which would lead Cas9 to disrupt only the core of the CTCF binding motif (Fig. 6A). We transfected cells with Cas9 and either the targeting or a scrambled sgRNA control...
  9. ...KHILL measures change in terms of k-mer representation and frequency across days, it is sensitive to uneven coverage and the noise characteristic of metagenomic sequencing in a way that marker-based analysis is not. To screen the noisiest time points and assure even coverage, we calculated the alpha...
  10. ...it is true in mammalian cells is unknown.We tested the first prediction by asking whether there was increased overlap between the growth genes identified using RH-BSA and those identified in loss-of-function CRISPR (Hart et al. 2015; Wang et al. 2015) and CRISPRi screens (Gilbert et al. 2014). Contrary...
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