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TSAT: Efficient evaluation software for NGS data of phage/mirror-image phage display selections
Tim Altendorf1, Jeannine Mohrlüder2, Dieter Willbold1
1Institut für Biologische Informationsprozesse, IBI-7, Forschungszentrum Jülich, Jülich, Germany; Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
Biophysical Reports
|June 23, 2024
Summary
Phage display and mirror-image phage display are powerful techniques for identifying specific binders. A new software tool, TSAT, simplifies the analysis of next-generation sequencing data from these selections, reducing workload.
Area of Science:
- Biotechnology
- Molecular Biology
- Bioinformatics
Background:
- Phage display and mirror-image phage display are established methods for identifying target-specific binders.
- Next-generation sequencing (NGS) enhances data extraction from phage display selections, improving binder identification.
- Analyzing NGS data from phage display can be labor-intensive, posing a challenge for researchers.
Purpose of the Study:
- To develop a user-friendly software tool for efficient analysis of peptide sequence data.
- To address the increased workload associated with NGS analysis of phage display selections.
- To facilitate the selection of effective binders through streamlined data interpretation.
Main Methods:
- Development of TSAT (target-specific analysis tool) software.
- Application of TSAT to analyze peptide sequence data from NGS of phage display selections.
- Evaluation of TSAT's efficiency and user-friendliness.
Main Results:
- TSAT provides a user-friendly interface for analyzing complex peptide sequence data.
- The software efficiently processes data from NGS of phage display selections.
- TSAT aids in the identification and selection of high-affinity binders.
Conclusions:
- TSAT is an effective solution for managing the analytical workload of NGS in phage display.
- The tool enhances the efficiency of identifying specific binders.
- TSAT supports researchers in leveraging NGS data for improved binder discovery.

