Scanning arrays were comprised of 2464 BACs selected at approximately megabase intervals along the genome.
SNP arrays are comprised of a large number of known polymorphisms that allow an individual to be genotyped at all sites simultaneously which reduces the overall cost per data point [ 13].
These arrays are comprised of 46,228 probe sets representing over 6,703 miRNA sequences (71 organisms) from the Sanger miRNA database (V.11) and an additional 922 sequences of human small nucleolar RNA (snoRNA) and small Cajal body-specific RNA from the Ensemble database and snoRNABase.
The array is comprised of two acoustic vector-sensors (AVSs) which are located at the fore of the glasses' temples.
Antenna array is comprised of a set of array elements sequentially arranged based on given discipline.
The array is comprised of 108 63-mer probes.
The final array is comprised of 1,091,987 probes (47,845 probesets) with a mean coverage of 22 probes/transcript.
The array is comprised of accessions representing a range of growth habit, row type, usage and origin.
Each array is comprised of >48,000 probes derived from human genes in the NCBI RefSeq and UniGene databases.
The array is comprised of 8 parallel fsPAG lanes, each housing 12 separation units in series with a 4.5 mm unit-to-unit distance.
