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  1. ...construction of RNA-seq libraries. Genome Res 22: 134–141. Halvardson J, Zaghlool A, Feuk L. 2013. Exome RNA sequencing reveals rare and novel alternative transcripts. Nucleic Acids Res 41: e6. Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, Kokocinski F, Aken BL, Barrell D, Zadissa A, Searle S, et...
  2. ...-treated and control ES cells were dissociated into single cells with 0.25% trypsin-EDTA. The dissociated cells were washed twice with 0.04% BSA in PBS and resuspended to a concentration of 1000 cells per microliter. Then the cells were subjected to scRNA-seq. Single-cell libraries were generated using the chromium...
  3. ...a reduction of the available volume in which the transposase can operate. Tagmentation of subpicogram amounts of cDNA In order to test the lower limit of input DNA required for tagmentation, we generated libraries from 500, 100, 10, 1, and 0.1 pg of double-stranded DNA. We successfully obtained RNA-seq...
  4. ...Spadden Gardener 2013; Shemesh et al. 2013; Wang et al. 2013). As such, there remains a strong need for robust in vitro methods to capture midrange contiguity information for de novo assembly. Transposase-mediated library construction, or ‘‘tagmentation,’’ utilizes a hyperactive Tn5 transposase to both fragment...
  5. ...PDAC cell lines, and hTERT-HPNE cell lines were retrieved from public repositories (see Supplemental Material).RNA-seq and DNA-seq library preparation and sequencingRNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep kit for Illumina, followed by sequencing on the Illumina HiSeq X...
  6. ...for transposase-accessible chromatin using sequencing (ATAC-seq) and RNA sequencing (RNA-seq) on human induced pluripotent stem cell–derived cardiomyocytes (iPSC-CMs) to nominate cCREs (Corces et al. 2017). We then linked key regulatory elements to MYH6 and MYH7. We characterize the effects of epigenetic editing...
  7. ...years since the initial description of transposase-based methods to prepare high-throughput sequencing libraries, or “tagmentation,” in which a hyperactive transposase is used to simultaneously fragment target DNA and append universal adapter sequences. Tagmentation effectively replaced a series...
  8. ...Bac transposase expression vector, A3-helper was from stocks stored in our laboratory. The CRISPR library delivery vector, pB-CRISPR, was constructed with the process described in the Supplemental Materials. The target vectors used to test the knockout efficiency of pB-CRISPR was constructed using library...
  9. ...: 779–785. Gertz J, Varley KE, Davis NS, Baas BJ, Goryshin IY, Vaidyanathan R, Kuersten S, Myers RM. 2012. Transposase mediated construction of RNA-seq libraries. Genome Res 22: 134–141. Grunenwald H, Baas B, Goryshin I, Zhang B, Adey A, Hu S, Shendure J, Caruccio N, Maffitt M. 2011. Nextera PCR...
  10. ...Beauty ( SB )-mobilized T2/Onc transposons have been used to identify common insertion sites (CISs) associated with tumor formation. Recurrent sites of transposon insertion are commonly identified using ligation-mediated PCR (LM-PCR). Here, we use RNA sequencing (RNA-seq) data to directly identify...
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