Cancer Panels
Cancer panels using next generation sequencing (NGS) technology target specific genes or mutations relevant to a particular cancer phenotype.
Cancer panels using next generation sequencing (NGS) technology target specific genes or mutations relevant to a particular cancer phenotype.
Single-cell ATAC-Seq (scATAC-Seq) utilizes microfluidics and molecular barcoding to investigate chromatin accessibility in hundreds to thousands of individual nuclei from a single sample.
Methylation sequencing is the process in which DNA methylation is quantified using sodium bisulfite and subsequent nucleotide base conversion. To uncover the methylome, GENEWIZ uses wet and dry lab solutions, including Methyl-Seq, for global whole genome and targeted 5-methylcytosine (5mC) detection.
TargetGxOne™ CUSTOM GENE PANELS GENEWIZ TargetGxOne™ custom gene panels provide targeted resequencing of any gene of interest via next generation sequencing (NGS). Custom resequencing can provide information on point mutations, insertions/deletions (INDELs), copy number variations (CNVs), and gene rearrangements for your specific genes of interest. When looking at multiple genes and/or multiple samples, next…
GENEWIZ Custom Short-Read Amplicon Sequencing service routinely sequences pre-made amplicons on Illumina platforms to answer a myriad of biological questions.
GENEWIZ Long-Read Amplicon Sequencing offers ultra-deep, contiguous amplicon sequencing for sequences up to 10,000 bp.
Immune Profiling couples ultra-deep sequencing of V(D)J regions and customized bioinformatics to provide comprehensive characterization of the entire B-cell receptor (BCR) and T-cell receptor (TCR) repertoire.