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F1000Research
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December 21, 2016
Genomic variant annotation workflow for clinical applications
Thomas Thurnherr, Franziska Singer, Daniel J Stekhoven, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 22, 2024
Moving Toward Metaproteogenomics: A Computational Perspective on Analyzing Microbial Samples via Proteogenomics
Franziska Singer, Mathias Kuhring, Bernhard Y Renard, et al.
Psychopharmacology
|
October 12, 2018
Effects of the experimental administration of oral estrogen on prefrontal functions in healthy young women
Tobias Sommer, Katharina Richter, Franziska Singer, et al.
NAR Genomics and Bioinformatics
|
June 19, 2023
scROSHI: robust supervised hierarchical identification of single cells
Michael Prummer, Anne Bertolini, Lars Bosshard, et al.
Bioinformatics (Oxford, England)
|
December 31, 2020
SCIM: universal single-cell matching with unpaired feature sets
Stefan G Stark, Joanna Ficek, Francesco Locatello, et al.
Nature Communications
|
November 27, 2023
Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in ovarian cancer
Arthur Dondi, Ulrike Lischetti, Francis Jacob, et al.
Bioinformatics (Oxford, England)
|
May 23, 2023
gExcite: a start-to-end framework for single-cell gene expression, hashing, and antibody analysis
Linda Grob, Anne Bertolini, Matteo Carrara, et al.
Briefings in Bioinformatics
|
December 23, 2017
Bioinformatics for precision oncology
Jochen Singer, Anja Irmisch, Hans-Joachim Ruscheweyh, et al.
Plos Computational Biology
|
June 3, 2022
scAmpi-A versatile pipeline for single-cell RNA-seq analysis from basics to clinics
Anne Bertolini, Michael Prummer, Mustafa Anil Tuncel, et al.
Communications Biology
|
August 10, 2023
Dynamic thresholding and tissue dissociation optimization for CITE-seq identifies differential surface protein abundance in metastatic melanoma
Ulrike Lischetti, Aizhan Tastanova, Franziska Singer, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
F1000Research
|
December 21, 2016
Genomic variant annotation workflow for clinical applications
Thomas Thurnherr, Franziska Singer, Daniel J Stekhoven, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 22, 2024
Moving Toward Metaproteogenomics: A Computational Perspective on Analyzing Microbial Samples via Proteogenomics
Franziska Singer, Mathias Kuhring, Bernhard Y Renard, et al.
Psychopharmacology
|
October 12, 2018
Effects of the experimental administration of oral estrogen on prefrontal functions in healthy young women
Tobias Sommer, Katharina Richter, Franziska Singer, et al.
NAR Genomics and Bioinformatics
|
June 19, 2023
scROSHI: robust supervised hierarchical identification of single cells
Michael Prummer, Anne Bertolini, Lars Bosshard, et al.
Bioinformatics (Oxford, England)
|
December 31, 2020
SCIM: universal single-cell matching with unpaired feature sets
Stefan G Stark, Joanna Ficek, Francesco Locatello, et al.
Nature Communications
|
November 27, 2023
Detection of isoforms and genomic alterations by high-throughput full-length single-cell RNA sequencing in ovarian cancer
Arthur Dondi, Ulrike Lischetti, Francis Jacob, et al.
Bioinformatics (Oxford, England)
|
May 23, 2023
gExcite: a start-to-end framework for single-cell gene expression, hashing, and antibody analysis
Linda Grob, Anne Bertolini, Matteo Carrara, et al.
Briefings in Bioinformatics
|
December 23, 2017
Bioinformatics for precision oncology
Jochen Singer, Anja Irmisch, Hans-Joachim Ruscheweyh, et al.
Plos Computational Biology
|
June 3, 2022
scAmpi-A versatile pipeline for single-cell RNA-seq analysis from basics to clinics
Anne Bertolini, Michael Prummer, Mustafa Anil Tuncel, et al.
Communications Biology
|
August 10, 2023
Dynamic thresholding and tissue dissociation optimization for CITE-seq identifies differential surface protein abundance in metastatic melanoma
Ulrike Lischetti, Aizhan Tastanova, Franziska Singer, et al.
Page
of 3