Welcome to Dr. Irtisha Singh’s Laboratory

From Code to Function: Mapping the Molecular Landscape of Normal and Cancer Cells

About

We are an integrative computational and experimental laboratory at Texas A&M University.

At Singh Lab, we merge cutting-edge computational methodologies, statistical modelling and machine learning approaches with sophisticated molecular assays to decode functional regulatory programs in normal/cancer cells. By leveraging integrative data analysis, high-throughput functional screens and CRISPR perturbation technologies, we aim to decipher the molecular states of normal/cancer cells and how their dysregulation drives the pathophysiology in malignancies. We have established multidisciplinary collaborations with physician scientists at Emory Winship Cancer Institute, University, Stanford Medicine and Dana Farber Cancer Institute. We have also built strong on-campus collaborations with researchers at Department of Biomedical Engineering and Department of Biology.

Key Research Areas

Computational Biology (Statistical Modelling and Machine Learning)

Our computational biology framework draws on our in-house and collaborative high throughput molecular readouts as well as the ones available through public domains. We leverage interpretable statistical models like regularized regressions etc, to determine the regulatory elements that impact gene expression. Our lab focuses on using machine learning techniques and statistical models to decode how epigenetic states influence co-transcriptional RNA processing and gene expression.

Dysregulation of RNA Processing as Driver of Cancer

Dysregulated intronic polyadenylation (IPA) is a novel cancer-associated phenomenon. Our studies reveal IPA isoform dysregulation in Chronic Lymphocytic Leukemia (CLL) and Multiple Myeloma (MM), yet its functional impact in MM remains unclear. mRNA events are key contributors to cancer pathogenesis, making it essential to identify IPA-targeted genes and their role in tumorigenesis. Understanding IPA dysregulation could uncover an alternative mechanism by which cancer cells enhance proliferation and growth without genetic disruptions.

Interrogate the functional role of non-coding transcripts generated by IPA

Transcription of RNAs from genomic loci of protein-coding genes is widely accepted to be translated into proteins. We were surprised to find a substantial overrepresentation of IPA isoforms with limited coding potential. The functional roles of these RNA isoforms remain unexplored. In the lab we are interrogating the role of ncpRNAs with a broader goal of informing the types of biological function mediated by non-coding IPA isoforms.

Dissecting Role of Epigenetics in oncogenic transformation

While genetic alterations are central to cancer, epigenomic changes also play a crucial role in driving normal cells toward a tumorigenic state. Enhancers, non-coding regulatory elements bound by transcription factors, mediators, and RNA Pol II, establish connections with gene promoters to regulate cell-type-specific expression. Their dysregulation is implicated in many cancers. In our lab, we explore how epigenetic states shape transcriptional profiles to drive tumorigenesis.

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"Expression of IPA isoforms is often robust—they do not represent ‘cryptic’ events or ‘transcriptional noise’—and is regulated across normal cells and dysregulated in cancer."

Dr. Irtisha Singh

Principle Investigator

Our Funding Sources

F.A.Q.

Your Questions, Answered!

If you’re interested in joining our team, visit our “Positions & Contact” page to view open opportunities and application instructions. Feel free to reach out via email with your CV and a brief description of your research interests.

Yes, we welcome motivated undergraduates to gain hands-on research experience. Check our “Positions & Contact” page for more details and application steps.

We occasionally offer summer internships for students interested in computational biology and experimental research. Announcements for such opportunities will be posted on our website.

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