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  1. ...polymorphism (RFLP) analysis 574 Genomic DNA was amplified by PCR using gene-specific primers and Diastar Taq DNA 575 polymerase (Solgent). The following primer pairs were used for PCR amplification: for 576 EFTUD2: 5′–AGAGTGGCTGTGATACCG–3′ (forward) and 5′–577 GAAGCACTAACAGTGAGGG–3′ (reverse); for KPNB1: 5...
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  2. ...phenotype (Nevins and Potti 2007). One key application of signature scoring is cell annotation, as it offers a highly efficient and reliable method for classifying cells into types and states (Neftel et al. 2019). Notably, the quality of gene signatures plays a critical role in this process, as the accuracy...
  3. ...were prepared with a starting amount of 300 ng and amplified in 14 PCR cycles. Libraries were profiled in a High Sensitivity DNA on a 2100 Bioanalyzer (Agilent Technologies) and quantified using the Qubit dsDNA HS Assay kit, in a Qubit 2.0 Fluorometer (Life Technologies). All libraries from the two...
  4. ...the random induction theory of mutations in general.DNA methylation change caused by tissue culture varies and can be inherited in woodland strawberryWe found that the three CK plants had quite different DNA methylation levels (Supplemental Table 5), suggesting that the DNA methylation level itself is highly...
  5. ...16 TRs are genomic sequences composed of tandemly arranged DNA repeat units. TRs are broadly categorized into short17 tandem repeats (STRs) and long tandem repeats (LTRs) based on repeat unit length. STRs typically consist of 1–6 base18 pair (bp) repeat units, whereas LTRs can span hundreds of base...
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  6. ...). Briefly, total 569 cell RNA was extracted from K562 cells and converted to cDNA using SMARTer scribe reverse 570 transcriptase. The specific genes were amplified from cDNA by gene specific primer in the exonic 571 region of IPA along UPM followed by a PCR with nested gene specific primer. The amplified...
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  7. ...complementary to the first adapter, and the other DNA end was ligated to the second adapter (Fig. 1D, blue). Following PCR amplification using primers complementary to both adapters, the resulting libraries were submitted for high-throughput sequencing. The resulting sequencing reads were mapped to the yeast...
  8. ...–protein integration (focusing on those demonstrating successful cross-omics alignment). stMSA generated the most expressive latent representations, achieving the lowest Geary's C (minimizing spatial randomness) and highest Moran's I (maximizing spatial dependency) (Fig. 4G). This underscores stMSA's ability...
  9. ...(PSI) among groups with or without SF3B1 mutation. (E) Validation of the differential splicing associated with SF3B1 mutation with RT-PCR experiments in isogenic K562 and Nalm6 cell lines. (F) Minigene assays workflow. HEK293T cells were cotransfected with minigenes and either SF3B1wt or SF3B1K700E...
  10. ...before (DAP-seq) and after PCR amplification (ampDAP-seq), where the amplification depletes the library of DNA methylation. MBD5 and MBD6 showed sequence enrichment, but only for DAP-seq, where DNA methylation was present, and with binding site profiles that closely match those identified by Ch...
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