Functional Genomics Contract Screens

We Help Find the Genes that Matter to You!

End-to-end or modular service options for life science researchers seeking to uncover functional genes important for phenotypic responses, disease progression, therapeutic responses, signaling pathways, or genetic requirements for drug mechanism of action or resistance.

Overview

Cellecta’s Contract Projects Group supports biotech, pharma, government, and academic labs looking to identify gene function, mechanisms of action, drug response markers, or disease drivers with fully customized solutions including CRISPR and RNAi screening, perturbation-based single-cell transcriptomics, and engineered cell line development. We provide quality data on time and within budget to research laboratories—saving you the cost and burden of building internal screening infrastructure.

Custom Research Solutions

  • Full-Service CRISPR & shRNA Screens
  • Comprehensive Cell Line Engineering
  • Perturb-seq and Single-Cell CRISPR Screens
  • Custom Library Development & Sequencing
  • Immune Profiling & Repertoire Sequencing
  • Bioinformatics Analysis Capabilities

The Cellecta Advantage

  • Deep Functional Genomics and Cell Biology Expertise
  • Collaborative Project Scoping to Define Assay Design and End Goals
  • Flexible Project-Based Engagement Models
  • Results-Focused Deliverables
  • Proven Workflows Established in House by Experienced Scientists
  • Published Outcomes & Peer Credibility
  • Transparent Timelines & Pricing
  • Confidentiality

Record of Success

Sample Typical Projects

  • CRISPR drug response or resistance screens with genome-wide or targeted sgRNA libraries
  • Making and screening UTR-reporter libraries for translational control regions
  • Perturb-seq screens using the most appropriate scRNA-seq platform
  • CRISPR screens with non-Cas9 systems such as dCas9-VPH, dCas9-KRAB, Cas13d, etc.
  • Inducible knock-in/knock-out cell line development

Get Started

Schedule a Technical Consultation

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Request a project quote using one of the links below: