DNA

Here at SMCS-PSI, we handle high-throughput sequencing data involving, ChIP-Seq, Microarray data, DAPseq data, and Bisulphite genomic sequencing for genomic research. We try to gain meaningful insight by implementing machine learning models on the available data.

At SMCS-PSI, we are committed to unlocking the full potential of high-throughput sequencing data. Our team of experts specializes in analyzing complex datasets, including ChIP-Seq, Microarray, DAP-seq, Bisulfite genomic sequencing and etc, to uncover valuable insights that drive genomic research forward. By leveraging the power of machine learning models, we are able to extract meaningful patterns and relationships from the vast amounts of data at our disposal. Our robust analytical approach allows us to tackle even the most challenging research questions, providing our clients with the actionable intelligence they need to make informed decisions and advance their scientific endeavors.

Gene locus

Our SMCS-PSI team also handles Genelocus Specific Analysis for researchers looking to unravel the complexities of gene locus-specific studies. Whether you're working with high-throughput sequencing data involving techniques like ChIA-PET, SPRITE, or ChIA-Drop, our team has the expertise to help you make sense of it all. Our advanced analytics capabilities allow us to dive deep into enhancer or super-enhancer regions, also proteins stabilising such regions to propel your understanding further at gene locus level. With our SMCS-PSI Genelocus Specific Analysis, you can trust that you're getting the most comprehensive and reliable results, empowering you to make informed decisions and drive your work forward. Don't let the challenges of gene locus-specific analysis hold you back. Partner with us and let our team of experts guide you through the process, ensuring that you get the answers you need to unlock the secrets of the genome.

Genomewide

Our SMCS-PSI team is highly skilled in conducting comprehensive genome-wide analyses. We have extensive expertise in studying cutting-edge techniques such as Hi-C, GAM, and ATAC-seq, which provide invaluable insights into the complex mechanisms governing gene regulation and chromatin organization. By leveraging our deep understanding of these advanced genomic profiling methods, we are able to deliver meaningful and impactful results that drive scientific progress. Our team's rigorous approach and commitment to excellence ensure that our genome-wide studies yield reliable and actionable insights that our clients can trust. Whether you're exploring the three-dimensional architecture of the genome, investigating chromatin accessibility, or delving into the intricate interplay of regulatory elements, our SMCS-PSI team has the specialized knowledge and capabilities to tackle your most challenging genome-wide research objectives.

Single cell sequencing and single cell methylome sequencing

Our SMCS-PSI team has been at the forefront of single cell sequencing technology, delivering meaningful insights that drive scientific breakthroughs. Through our advanced single cell sequencing analysis we can locate gene expression and DNA methylation patterns at the individual cell level, providing unprecedented resolution into cellular heterogeneity and function. Our single cell sequencing workflows leverage the latest microfluidic and next-generation sequencing platforms to capture the unique molecular signatures of thousands of individual cells simultaneously. This coupled with our expertise in single cell methylome sequencing, we can also map the epigenetic landscape of individual cells, revealing how regulatory mechanisms shape cellular identity and response to stimuli. This powerful combination of transcriptomic and epigenomic profiling at single cell resolution is transforming our understanding of biological systems in health and disease. Trust our SMCS-PSI team to deliver the high-quality single cell sequencing data and analysis you need to advance your most critical research initiatives. Contact us today to learn more about our single cell sequencing capabilities.