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Each input sample is read into SM along with (M - 1) previous sample points to perform filter operation.
Data from all samples were read into SAS 8.2 (SAS Institute Inc ,Cary, NC, USA).
The light produced from the samples was read by a plate reading luminometer, Victor X (Perkin Elmer, Waltham, MA).
The light produced from the samples was read by a standard plate reading luminometer.
First, the raw data from GenePix was read into R.
The PACAP-38 concentrations of the unknown samples were read from calibration curves.
The raw data from CEL files were read into R.
The genomic reference chromosomes were partitioned into consecutive non-overlapping bins of 100,000 bp and the percentage of reads mapping to each bin from each sample was recorded.
High-quality sequence reads from each sample are initially clustered into operational taxonomic units (OTUs) at a defined level of similarity.
Individual read files for each sample were concatenated into a single.fastq file.
Sequenced reads from each sample were then analyzed independently, assigning reads to genes and isoforms that were identified de novo.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com