B260

B260 Bioinformatik der Genomik und Systemgenetik
IDI:(DE-He78)B260-20160331

Recent Publications

All known publications ...
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Functional phenotyping of genomic variants using joint multiomic single-cell DNA-RNA sequencing.
Nature methods nn, nn () [10.1038/s41592-025-02805-0]  GO BibTeX | EndNote: XML, Text | RIS

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Unveiling genetic signatures of immune response in immune-related diseases through single-cell eQTL analysis across diverse conditions.
Nature Communications 16(1), 7134 () [10.1038/s41467-025-61192-4]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Optimized summary-statistic-based single-cell eQTL meta-analysis.
Scientific reports 15(1), 28407 () [10.1038/s41598-025-08808-3]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships.
Nature biomedical engineering nn, nn () [10.1038/s41551-025-01437-1]  GO BibTeX | EndNote: XML, Text | RIS

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Complex genetic variation in nearly complete human genomes.
Nature 644(8076), 430-441 () [10.1038/s41586-025-09140-6]  GO BibTeX | EndNote: XML, Text | RIS

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From spots to cells: Cell segmentation in spatial transcriptomics with BOMS.
PLOS ONE 20(6), e0311458 - () [10.1371/journal.pone.0311458]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Proteome-wide determinants of co-translational chaperone binding in bacteria.
Nature Communications 16(1), 4361 () [10.1038/s41467-025-59067-9]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Cell2fate infers RNA velocity modules to improve cell fate prediction.
Nature methods 22(4), 698-707 () [10.1038/s41592-025-02608-3]  GO BibTeX | EndNote: XML, Text | RIS

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The Federated European Genome-Phenome Archive as a global network for sharing human genomics data.
Nature genetics 57, 481–485 () [10.1038/s41588-025-02101-9]  GO BibTeX | EndNote: XML, Text | RIS

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Journal Article (Erratum/Correction)  ;  ;  ; et al
Author Correction: Complex genetic variation in nearly complete human genomes.
Nature nn, nn () [10.1038/s41586-025-09547-1]  GO BibTeX | EndNote: XML, Text | RIS

All known publications ...
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 Record created 2018-10-04, last modified 2022-03-18



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