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high-throughput sequencing services

Awarded to Biomarker Technologies (BMK) GmbH, EDINBURGH GENETICS LIMITED, GENEWIZ UK LIMITED +1 more

CELL THERAPY CATAPULT LIMITED(buyer)

Published
Published 29 August 2025
Deadline
Closed 12 September 2025

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Overview

Cell Therapy Catapult Limited procured high-throughput sequencing services on a fee-per-service basis to support cell and gene therapy development and process characterization. The contract, awarded on 5 December 2025, was split across six lots covering short-read sequencing, bulk and single-cell RNA sequencing, AAV genome sequencing, and Sanger sequencing, with four providers selected: Biomarker Technologies (BMK) GmbH, Edinburgh Genetics Limited, Genewiz UK Limited, and Novogene (UK) Company Limited.

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Lots (6)

  • High-throughput short-read sequencing of libraries generated by CGT Catapult (i.e., sequencing-only)

    For this service, the provider will receive pre-prepared library pools from CGT Catapult ready for sequencing. These libraries may originate from various sources and experimental designs, representing the final product of CGT Catapult's library preparation efforts. The service should include a Quality Control (QC) step to ascertain whether the provided library sample is considered suitable for downstream sequencing. This QC should evaluate factors such as the presence of adapter artifacts and confirm a minimum yield/concentration. The required throughput per run will vary based on project needs, but typical requirements for human cell-based applications often range from 20 to 30 million reads per sample for messenger RNA profiling and from 40 to 50 million reads per sample for total RNA profiling. Readouts other than gene expression may have other minimum read number requirements. Sequencing should be performed with flexibility for both single-read and paired-end sequencing modes, with read lengths up to 150 bp. The option for specifying read strandedness should also be available, as required by the experimental design. Typically, sample QC should be completed within 1-5 business days of receipt of the library pool(s). Sequencing run completion and raw data delivery are expected to be from 2 weeks to 3 months.

    Won by GENEWIZ UK LIMITED
  • Bulk RNA sequencing

    This service will typically involve library preparation and sequencing from cell pellets or isolated RNA samples provided by CGT Catapult. These samples will be derived from various cell lines undergoing different processes. The sequencing throughput, read strandedness, and mode will be contingent on project needs. Additionally, the provider should offer tiered support for data analysis, ranging from raw data processing (e.g., demultiplexing, adapter trimming, read alignment, quantification of gene counts) to statistical analysis (e.g., differential gene expression analysis, clustering) and functional enrichment analysis (e.g., pathway enrichment analysis), contingent on project needs. Sample QC and library preparation typically take 3-14 business days. Sequencing run completion and raw data delivery are expected to be from 2 weeks to 3 months. Tiered data analysis can take 2 weeks to 2 months, depending on the complexity of the analysis.

    Won by Biomarker Technologies (BMK) GmbH
  • Bulk small RNA sequencing

    For bulk small RNA sequencing, the provider will generally receive cell pellets, cell culture supernatant, or extracted RNA samples from CGT Catapult. These samples will be used to profile microRNAs and other small non-coding RNAs. The provider should also offer tiered support for data analysis, ranging from raw data processing to statistical analysis, including annotation to known microRNAs or other small RNA types (e.g., piRNAs) and de novo small RNA discovery, contingent on project needs. Sample QC and library preparation typically take 3-14 business days. Sequencing run completion and raw data delivery are expected to be from 2 weeks to 3 months. Tiered data analysis can take 2 weeks to 2 months, depending on the complexity of the analysis.

    Won by EDINBURGH GENETICS LIMITED
  • Single-cell RNA sequencing (scRNA-seq) of cryopreserved/fixed samples

    This service will involve library preparation and sequencing where cryopreserved or fixed cell samples will be provided by CGT Catapult. The throughput for single-cell sequencing should accommodate varying project sizes with regards to number of samples, number of profiled cells per sample, and number of reads to obtain per cell. Sample QC and library preparation typically take 3-14 business days. Sequencing run completion and raw data delivery are expected to be from 2 weeks to 3 months.

    Won by GENEWIZ UK LIMITED
  • AAV genome sequencing

    This service will involve analysis of AAV samples (final product) to confirm packaged AAV genome sequence and detect any DNA impurities in the sample. Different AAV serotypes may be used. For a sequencing-only service, AAV genomes will be extracted and libraries generated at CGT Catapult and sent to the provider for downstream sequencing. For end-to-end QC analysis of AAV samples, CGT Catapult samples will be sent to the provider for library generation and QC. Long-read sequencing using PacBio instrumentation will be performed to assess AAV genome integrity, while short-read sequencing will be utilized to confirm sequence of AAV vectors and identify contaminants. Specific requirements for this AAV analysis will depend on project needs. Sample QC and library preparation typically take 3-14 business days. Sequencing run completion and raw data delivery are expected to be from 2 weeks to 3 months. Tiered data analysis can take 2 weeks to 2 months, depending on the complexity of the analysis.

    Won by NOVOGENE (UK) COMPANY LIMITED
  • Sanger sequencing

    This service is required for targeted sequencing applications, such as confirming effective gene knockout after CRISPR-Cas9 editing, validating the successful insertion of gene cassettes, or verifying specific point mutations. CGT Catapult will typically provide purified DNA samples (e.g., plasmid DNA, PCR amplicons) for this service. The provider should offer robust quality control to ensure sample suitability, followed by sequencing and primary data analysis, including trace visualization and base calling. The expected output is high-quality sequence reads for individual targets, enabling precise validation of genetic modifications. This service typically takes 1-5 business days from sample receipt.

    Won by GENEWIZ UK LIMITED

Key details

Country
United Kingdom
Status
In delivery
Category
Services
Procedure
Open
SME suitable
Yes
Published
29 August 2025
Questions by
4 September 2025
Deadline
Closed
Classification (CPV)
Research and development services and related consultancy services

Award outcome

Award date
5 December 2025
Contract period
3 November 2025 → 2 November 2026
Winners
  • Biomarker Technologies (BMK) GmbH
  • EDINBURGH GENETICS LIMITED
  • GENEWIZ UK LIMITED
  • NOVOGENE (UK) COMPANY LIMITED

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Notice history

Every published notice in this contracting process, newest first.

  1. Contract

    5 December 2025

  2. Contract Notice

    29 August 2025

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