At the Northwest Genomics Center (NWGC), we perform NGS and genotyping. We utilize Illumina sequencing and genotyping platforms to provide high-quality sequencing and genotyping data. We accept projects ranging from a few samples to several thousand and have the knowledge and experience to customize projects to fit any investigator’s needs.<\/p>\n
We have produced short-read sequence data for more than 260K samples\u2014including 100K genomes, 48K RNA-Seq, 64K exomes + custom capture, 48K samples for other types of sequencing (e.g., snRNA-seq, Chip-Seq, amplicon sequencing, MIPS etc.), and we have processed more than 417K genotyping arrays and 50K DNA methylation profiles since the NWGC was established. In addition to the short-read sequence data, we have processed over 550 long-read samples. (Updated April 2024).<\/p>\n
Since our founding in 2009, the Northwest Genomics Center has played a major role in the data generation and methods development in support of the following genomic resource projects:<\/p>\n
AGTC<\/strong> \u2013 University of Washington Center for Mendelian Genomics<\/p>\n PGRN<\/strong> \u2013 Pharmacogenomics Global Research Network<\/p>\n SeattleSeq Annotation<\/strong><\/p>\n TOPMed<\/strong> \u2013 Trans-Omics for Precision Medicine<\/p>\n NHLBI Exome Sequencing Project (ESP) Exome Variant Server<\/strong><\/p>\n GREGoR Consortium<\/strong> \u2013 Genomics Research to Elucidate the Genetics of Rare Disease<\/p>\n Emerge Network<\/strong> – Electronic Medical Records and Genomics<\/p>\n Stargazer<\/strong><\/p>\n CSER<\/strong> – Clinical Sequencing Evidence-Generating Research<\/p>\n Seattle Flu Alliance<\/strong><\/p>\n RS&G<\/strong> \u2013 UW NHLBI Resequencing and Genotyping Laboratory Center<\/p>\n All Of Us<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":" At the Northwest Genomics Center (NWGC), we perform NGS and genotyping. We utilize Illumina sequencing and genotyping platforms to provide high-quality sequencing and genotyping data. We accept projects ranging from a few samples to several thousand and have the knowledge and experience to customize projects to fit any investigator’s needs. We have produced short-read sequence data for more than 260K samples\u2014including 100K genomes, 48K RNA-Seq, 64K exomes + custom capture, 48K samples for other types of sequencing (e.g., snRNA-seq, Chip-Seq,…<\/p>\n