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Table 1 summarizes the read counts obtained from each of the sequencing runs.
For each of the sequencing reads, low-quality bases and the sequencing adapter were trimmed using LUCY and SeqClean.
Nevertheless, because 20 embryos were pooled to generate each of the sequencing libraries, the gene expression measurements represented averages across 20 embryos.
A Pdict library of each of the sequencing reads was created using the 5 40 bp region of each of the 100-bp reads.
We obtained about 10 and 20 million reads from control and infected mosquitoes, but more than 60% of reads in each of the sequencing libraries were not annotated.
For each of the sequencing reads, low-quality bases (Sanger base quality < 20) of 3' ends were first trimmed using in-house perl scripts and the sequencing adapters were then trimmed using Fastx toolkit (version 0.0.13) software.
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Otherwise, map returns a sequence such that element j is the result of applying function to element j of each of the sequences.
Three-dimensional structures of each of the sequences were built using MODELLER34 with five different random number seeds, and the structure with the lowest DOPE energy was chosen as the best model.
The positions of SSRs with respect to open reading frame (ORF) detected and annotation of sequences containing SSRs were also carried out to assign function to each of the sequences.
A specific target object was chosen for each of the sequences and used to test both object detection and tracking the target objects for each of the sequences.
Since the sequence x = θ belongs to each of the sequence spaces, the overlapping part of the proof is obvious.
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CEO of Professional Science Editing for Scientists @ prosciediting.com