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For example, Matrix Element Monte Carlo event generators can use the library for preparing and writing a header of an LHEF file in the form of HepML tags.
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It was unexpected that we obtained more sequences from CN samples than from BV samples (p < 0.05, data not shown) because the same amount of bacterial DNA was used for preparing the library for pyrosequencing.
He loved history and books of all kinds, really, and spent most of his free time in the library, preparing for his debating-team competitions.
As Bozic and his daughter wandered about, they saw that workers were preparing the library for a press conference, and so they hung around, Bozic jokingly scolding the workers for dragging tables and chairs along the wood floor.
Once, while the troupe was reading "Romeo and Juliet," the library was preparing to close for the night, forcing the play to end early.
Purified DNA were used to prepare the library for Illumina high-throughput sequencing using Illumina Single End ChIP-seq Sample Preparation Kit, as described in the manufacturer's protocol.
The concentration was further adjusted following qPCR to prepare the library for sequence analysis on an Illumina HiSeq instrument.
The remaining 27% are likely to be sequences from Symbiodinium, from genes that are expressed only at low levels in aposymbiotic Aiptasia, or from other organisms that were present in the culture used to prepare the library for Sanger sequencing.
For runs using MiSeq v2 kits, the following protocol was used to prepare the library for sequencing: beads harboring 25 fmol of single-stranded library fragments, usually about 1/5 of the final library volume after ligation of the second adapter, were mixed with 2.5 fmol of PhiX dsDNA control (Illumina, Inc., Hayward, CA) and EB buffer (Qiagen, Venlo, Netherlands) to 5 µl total.
For runs using MiSeq v3 kits, the following protocol was used to prepare the library for sequencing: beads harboring 32 fmol of single-stranded library fragments were mixed with 4.2 µl of 95% formamide and 10 mM EDTA and heated at 90°C for 2 min and 40 s, then cooled at room temperature for several minutes.
As we intended to obtain whole sequences of ChAP-DNA to avoid the bimodal distribution of sequence tags, DNA fragments containing ∼50 bp of inserted DNA, after ligation of adapter sequences, were selected to prepare the library for high-throughput sequencing by Illumina GAIIx.
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