Sentence examples for using a genome Analyser from inspiring English sources

The genomic DNA associated with ChIP'd samples was then sequenced using a genome analyser (ChIP-SEQ) to identify the C/EBPδ are C/EBPβ binding sites throughout the genome.

All libraries were sequenced in single read mode, using a Genome Analyser instrument (Illumina).

The cDNA libraries were sequenced using a Genome Analyser (GAIIx) in a paired-end approach with 2 × 36 cycles resulting in paired reads with a length of 36 nucleotides per read.

The libraries were sequenced using a Genome Analyser (GAIIx, Illumina, San Diego, CA, USA) in a single read approach with 76 cycles resulting in reads with length of 76 nucleotides.

Seven pools of RNA samples, representing each treatment and the control sample, which was common for all three treatments, were used to build libraries for high-throughput parallel sequencing using an Illumina Genome Analyser II (GAIIx).

A total of five libraries were multiplexed per sequencing reaction using an Illumina Genome Analyser II next-generation sequencer at the Weill Medicine School Sequencing Facility Cornell Universityy, New York City, NY, USA).

Sequence data: Targeted whole-exome sequencing was carried out for 31 (12 + 19) samples using an Illumina Genome Analyser IIx.

Two separate cDNA libraries were created from 1 μg RNA and sequenced by GATC Biotech AG (Konstanz, Germany) using an Illumina/Solexa Genome Analyser to create single-end reads of 101 bp length (80.5 million reads for T-oaks and 124.8 million reads for S-oaks; Solexa reads available at the SRA at EMBL-EBI [EMBL: ERP002577]).

Both libraries were sequenced by GATC Biotech AG (Konstanz, Germany) using an Illumina/Solexa Genome Analyser to create single-end reads of 36 bp length (12.5 million reads for T-oaks and 12.3 million reads for S-oaks; Solexa reads available at the Short Read Archive (SRA) at EMBL-EBI [EMBL: ERP002577]).

For whole transcriptome sequencing, we used an Illumina Genome Analyser II with 36 bp sequence reads length.

Libraries were sequenced on a Genome Analyser II as 54 bp paired-end reads.