Evidence map›Paper›PMID 41472884›Full record

ArticleNAR genomics and bioinformatics2025

Designing genetically stable multicopy gene constructs with the ChimeraUGEM web server.

Moritz Burghardt, Alon Diament, Tamir Tuller

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Moritz BurghardtDepartment of Biomedical Engineering, The Iby and Aladar Fleischman Faculty of Engineering, Tel Aviv 69978, Israel.
Alon DiamentDepartment of Biomedical Engineering, The Iby and Aladar Fleischman Faculty of Engineering, Tel Aviv 69978, Israel.
Tamir TullerDepartment of Biomedical Engineering, The Iby and Aladar Fleischman Faculty of Engineering, Tel Aviv 69978, Israel.ORCID 0000-0003-4194-7068

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High expression of heterologous proteins is often achieved by integrating multiple copies of a gene into a host. However, such multicopy systems are prone to genetic instability due to homologous recombination between identical sequences. We present the multisequence ChimeraMap (MScMap), an algorithm for designing multiple synonymous coding sequences that minimizes recombination risk while maintaining high expression. MScMap extends the ChimeraMap framework by selecting diverse nucleotide blocks from a host genome to encode the target protein, balancing host adaptation and sequence dissimilarity. We introduce heuristics for block selection and concatenation to reduce long common substrings, a known driver of recombination. Our method outperforms a multi-objective evolutionary algorithm in both genetic stability and predicted expression across a wide range of human proteins while being significantly faster. We also show that MScMap can also be used to reduce sequence repeats within a single coding sequence. A web tool for single and multicopy coding sequence optimization is available online.

Indexed as

AlgorithmsSoftwareHumansInternet

Identifiers

PMID41472884
PMCPMC12746100

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.