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Garvan researchers use the HiSeq System to identify cancer-associated variants in the germline.
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Whole-genome analysis screens for common fetal aneuploidies, providing women with information early in pregnancy.
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The clear majority of the Human Genome is non-coding. Although those billions of bases do not specifically encode genes, there are many hidden...
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Join NowThe importance of panel size in precisely measuring Tumor Mutational Burden in cancer composition
Read Article| Date | Publication | Title |
|---|---|---|
| Aug 6, 2018 | CNBC | Illumina CEO on the growth of DNA sequencing |
| Jul 20, 2018 | San Diego Union Tribune | Illumina continues to soar as its gene sequencers dominate the market |
| Jun 10, 2018 | The Washington Post | Rapid genome sequencing could revolutionize health care for acutely ill babies |