Single Cell ATAC-Seq

10x Genomics can process:
Up to 20K cells per sample (1-8 samples) using Chromium Epi Chromatin kit
Stringent Quality Controls – Your single cell submissions are assessed with Countess II to quantify cell concentration in suspension and cell viability before Chromium processing. Working carefully with your SeqMatic team to prepare your submission ensures superior cell recovery and GEM formation.
Scientific considerations for read depth – SeqMatic recommends a read depth of 25K read pairs per nucleus (50K individual reads; 25K from R1, 25K from R2). Higher and lower read depths are available depending on model organism requirements and/or project needs.
Preliminary Sequencing – After library preparation, SeqMatic prepared libraries are pooled to customer requirements and the final QC is checked via preliminary sequencing. Libraries are then normalized and re-pooled based on the nuclei count from the preliminary sequencing dataset.
World-class validation standard & practices – SeqMatic is equipped to ensure accurate, repeatable and reproducible results. SeqMatic’s quality program has been audited and approved as part of becoming a Clinical Laboratory Improvement Amendments (CLIA) and College of American Pathologists (CAP) certified sequencing facility. Our CLIA quality program requires the use of well-defined protocols to maintain the consistency and reproducibility of our NGS workflows. Thus, the samples will be processed in a CLIA environment.
Custom assay services – Our highly personalized sequencing services can be adapted to almost any (high and/or low throughput) sequencing workflow required by our customers so that we optimize the quality and quantity of data output.
Single cell ATAC workflow services include nuclei extraction, tagmentation and library generation, single cell barcoding, library amplification and sequencing, and a full suite of bioinformatics support.
From small projects with a few samples or low input to large scale high-throughput projects
Sequencing on NovaSeq 6000 and NovaSeq X Plus

We can process full workflows or accept your cells/tissue for nuclei dissociation, fresh/frozen nuclei, DNA or prepared libraries for sequencing.



Your S.F. Bay Area Advantage!
To maintain maximum sample viability, your samples can be transported to us
within 1 to 2 hours from any where in the SF Bay Area – Request a Quote!


Find other Research Publications from around the world!

Your S.F. Bay Area Advantage!
To maintain maximum sample viability, your samples can be transported to us
within 1 to 2 hours from any where in the SF Bay Area – Request a Quote!
Schupp, Patrick Georg. Clarifying the Transcriptional Profiles of Malignant Clones and Nonmalignant Cells of the Microenvironment through Multiscale and Multiomic Analysis of Individual Tumors. Diss. UCSF, 2023.
Barker, Scarlett J., et al. “Targeting Transferrin Receptor to Transport Antisense Oligonucleotides Across the Blood-Brain Barrier.” bioRxiv (2023): 2023-04.
Nair, Anup K., et al. “Generation of Isogenic hiPSCs with Targeted Edits at Multiple Intronic SNPs to Study the Effects of the Type 2 Diabetes Associated KCNQ1 Locus in American Indians.” Cells 11.9 (2022): 1446.
Find other Research Publications from around the world!






