![]() Illumina Complete Long Reads leverages "land-marks" on the original long, single-molecule fragment analyzed in combination with unmarked standard reads to generate highly accurate, complete long reads. "Illumina Complete Long Reads is the only offering that addresses the 5% of hard-to-read genic regions: at scale, with high accuracy, all on a single instrument, and with 90% less DNA input than other long read technologies." "This technology is unlike anything on the market and was engineered to meet and exceed our customers' needs," Aravanis said in his presentation. "We anticipate that, once up and running, this platform will have a large impact on our ability to support groups wanting to access our walk-up sequencing service, our human whole genome product, and our blended genome/exome product."Īs previously announced, Illumina is ramping up to ship 40-50 orders in this quarter and the company plans to ship more than 300 instruments in total this year.Īravanis also unveiled information about the technology behind Illumina Complete Long Reads, which generates highly accurate long reads in an efficient, scalable workflow. "We are always excited to welcome new technologies that will allow the scientific community to do more, and larger, experiments," Lennon said. "We know our customers are eager to embark on more, deeper, and larger genomic research driven by operational ease and lower costs."Īt AGBT, Niall Lennon, PhD, senior director of translational genomics at the Broad Institute of MIT and Harvard, presented alongside Aravanis, where he offered new data confirming that NovaSeq X Plus performance meets or exceeds that of the NovaSeq 6000. "We are thrilled to see the NovaSeq X Plus beginning to ship to our customers after years in research and development, and now their biggest aspirations can be realized: enabling projects never previously thought possible," said Aravanis. Aravanis announced today that the Broad Institute has received the world's first shipment. The NovaSeq X Series is Illumina's most powerful sequencing system, delivering an unprecedented combination of high throughput and accuracy, and featuring streamlined informatics, breakthrough sustainability advancements, and cost-effective sequencing economics.
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