Exact(1)
Microarray data from all eight experiments, including statistical analyses is briefly described in the "read me" document additional file 4. Microarray data from all eight experiments is separated by probe type in additional files 5, 6, and 7 (control, EBV, and KSHV probes, respectively).
Similar(59)
That is what the prophet Isaiah describes in the reading paired with our Torah-portion this week.
–What plan is described in the article read in class?
Why was it difficult to reconstruct the Enola Gay? 3. Explain to students that they will be creating museum exhibits for items that might be considered controversial to particular groups of people, as is the case for the Enola Gay as described in the article read in class.
Following the procedures described in the edgeR documentation, read count tables were loaded into R, normalized using the default method for edgeR (trimmed mean of M values, or TMM), and then tested for differential expression using the exactTest method.
The inspiration: Launched in 2012 by former Orange County Register reporter and art gallery director Debbie Talanian, Stella Proseyn's spring 2014 manifesto, as described in the show notes, reads: "This collection is about personal exploration.
As we described in the manuscript, average read-depths for mitochondrial DNA from WGS and WXS are 7,901x and 92x.
To test the performance of SDhaP for the assembly of polyploid haplotypes, we generate data in the same way as described in the previous section (notably, the reads and inserts are of the same lengths as those in the diploid simulations).
After repeat-masked, the BESs were self-BLASTed as described in the methods and no reads showed more than three matches to others, proving the high sensitivity of the RepeatScout pipeline.
After removing repeats/transposons [ 39] and known non-coding RNA (rRNA, tRNA, small nuclear RNA and small nucleolar RNA) [ 40] sequences as described in the Methods, the raw reads were mapped to the Yugu1 reference genome [ 35] using bowtie.
We removed 3'end sequences from the reads with phred quality values of 2. We randomly selected 30 million genomic reads using the process described in the Methods section (see section Simulated Read Sets) and determined their GC content.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.
Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com