The mission has always been clear: to improve human health by unlocking the power of the genome. That’s why we push the boundaries of genomic possibility so that researchers and clinicians can further accelerate their discoveries and applications to heal people and the planet. ...
Microbial Whole-Genome Sequencing Microbial Transcriptomics Infectious Diseases Human Microbiome Analysis Illumina Training All Microbial Genomics Research Fighting drug-resistant tuberculosis Experts agree that next-generation sequencing is the best weapon for comprehensively tracking multi-drug-resistant TB ...
The mission has always been clear: to improve human health by unlocking the power of the genome. That’s why we push the boundaries of genomic possibility so that researchers and clinicians can further accelerate their discoveries and applications to heal people and the planet. ...
Faster, more affordable, and higher quality sequencing with XLEAP-SBS chemistry on the NextSeq 1000 and NextSeq 2000 Systems Start doing more Improving human health can't wait The mission has always been clear: to improve human health by unlocking the power of the genome. That’s why we...
Large whole-genome sequencing (human, plant, animal) Small whole-genome sequencing (microbe, virus) checkmark checkmark checkmark checkmark checkmark Exome & large panel sequencing (enrichment-based) checkmark checkmark Targeted gene sequencing ...
自2003年人类基因组草图公布以来,基因组测序技术取得了巨大的进步,多种大规模平行测序(MPS)平台也如雨后春笋般迅猛增长。其中,全基因组测序(Whole Genome Sequencing,WGS)可无偏颇地检测各类基因突变,以提供整个基因组的全面视图,也是目前临床...
自2003年人类基因组草图公布以来,基因组测序技术取得了巨大的进步,多种大规模平行测序(MPS)平台也如雨后春笋般迅猛增长。其中,全基因组测序(Whole Genome Sequencing,WGS)可无偏颇地检测各类基因突变,以提供整个基因组的全面视图,也是目前临床及基础研究中常用到的技术之一。
Illumina sequencing and array technologies drive advances in life science research, translational and consumer genomics, and molecular diagnostics.
文献标题：Comparison between MGI and Illumina sequencing platforms for whole genome sequencing 主要研究方法及结果：该研究使用Illumina的NovaSeq 6000和MGI的MGISEQ-2000以及DNBSEQ-T7三种平台对两对来自韩国肺癌患者的正常组织和肿瘤组织进行了测序。然后，分别对体细胞和生殖系的单核苷酸变异（SNVs）和插入缺失（...
With the use of Illumina whole genome sequencing, genetic diversity among North American and European populations was explored with phylogenomic methods. Ploidy level was estimated by examining allele frequencies of read鈥恗apped homologous gene regions. Results indicate divergent populations between Europe...