Searching journal content for articles similar to Mullikin and Ning 13 (1): 81.

Displaying results 1-10 of 98
For checked items
  1. ...added to the reverse transcription reaction and incubated for 5 min. Beads were washed twice with 85% ethanol, dried, and eluted twice in nuclease-free water. cDNA preamplification was performed with i5_s and i7_s (300 nM each) primers and Phusion HF PCR Mastermix (Thermo Fisher Scientific). Six PCR...
  2. ...a comprehensive review to the theoretical properties and practical applications of k-mers in biodiversity genomics with a special focus on modeling.The genomics field has come a long way in the past quarter century. Sequencing and assembling even a partial was once a multibillion dollar accomplishment. Now...
  3. ...to transfect cells with individual sgRNA pairs (Laustsen and Bak 2019). To assemble RNPs with the sgRNA pairs, 6 µg Cas9 enzyme (0.6 µL of 10 µg/µL) was mixed with 1.6 µg (0.5 µL of 3.2 µg/µL) of each of the two sgRNAs in PCR tubes in no predefined order. RNPs were then stored at −20°C or used immediately...
  4. ...(525 ± 50 nm).Generation of barcoded reporter plasmidsSleeping Beauty reporter constructs used in this study were barcoded using a Gibson Assembly approach before introduction into K562 cells (Supplemental Fig. S3). The plasmid backbone to be barcoded was PCR amplified using pTR-GibsonBC-FW and p...
  5. ...). The latter were located closest to 3′ splice sites (Fig. 6L), suggesting that multiple SF3B1 binding sites assemble into complex binding patterns at 3′ splice sites. We then investigated the differences in binding between K562-SF3B1K700E/wt and K562-SF3B1wt/wt solely in the C3 cluster. We noticed that K562...
  6. ...multiplex SNP genotyping, has been widely adopted in numerous and diverse applications. The BeadArray platform enables the production of randomly assembled universal arrays and the analysis of any custom-built panel of SNPs, thus providing more flexibility than conventional microarrays (Oliphant et al. 2002...
  7. ...that includes SV discovery, local assembly of the allele with an SV, and SV genotyping across multiple samples (Fig. 1A). SVs were called in fetal brain clones (N = 3 brains and 41 clones) using Manta (Chen et al. 2016), and somatic events were selected based on clone-to-clone comparisons (Methods). Briefly...
  8. ...mRNAs for binding with YBX1 and suppress their stability (Goodarzi et al. 2015). Moreover, tsRNAs can frequently associate with translation machinery and related factors to participate in multiple layers of translation control, such as rRNA biogenesis, ribosome assembly, translation initiation...
  9. ...) and 105,509,782 fragments per time point. We mapped these fragments using HISAT2 (ver. 2.1.0) (Pertea et al. 2016) onto the AaegL5 AGWG assembly (obtained from VectorBase) (Giraldo-Calderón et al. 2015; Matthews et al. 2018; https://vectorbase.org/vectorbase/app) with a 78.48% average mapping rate...
For checked items

Preprint Server