Low-Pass Whole Genome Sequencing
Low-Pass Whole Genome Sequencing (LP-WGS or low-coverage whole-genome sequencing) is an inexpensive high-throughput technology for detecting genome-wide genetic variation in a multitude of species.
Hot Spot Cancer Panels
GENEWIZ next-generation sequencing based cancer panels provide a complete solution for your cancer research studies from experimental design to advanced bioinformatics analysis.
Cancer Panels
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)
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.
ChIP-Seq
ChIP-Seq (chromatin immunoprecipitation sequencing) combines the highly effective chromatin immunoprecipitation (ChIP) methodology and next generation sequencing (NGS) to analyze protein-DNA interactions.
ATAC-Seq
ATAC-Seq is a technique used to analyze the functional state of chromatin at the genome-wide level. The assay for transposase-accessible chromatin sequencing identifies regions of open chromatin and efficiently labels them for high-throughput sequencing.
Methylation Sequencing
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.
OncoGxOne
GENEWIZ OncoGxOne™ Discovery cancer panels provide comprehensive genomic analysis for cancer research, biomarker discovery, and patient stratification.
Custom-Targeted-Sequencing
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…
Custom Short-Read Amplicon Sequencing
GENEWIZ Custom Short-Read Amplicon Sequencing service routinely sequences pre-made amplicons on Illumina platforms to answer a myriad of biological questions.