Associated Papers
De novo detection of somatic variants in high-quality long-read single-cell RNA sequencing data.
Dondi A et al.
Genome Research, 2025
40107722 (PubMed )
Supplement: Supplemental_Table_S3.xlsx › Feuille_1
Spotlight on amino acid changing mutations in the JAK-STAT pathway: from disease-specific mutation to general mutation databases.
Hoffmann M et al.
Scientific Reports, 2025
39979591 (PubMed )
Supplement: 41598_2025_90788_MOESM2_ESM.docx
De novo detection of somatic variants in high-quality long-read single-cell RNA sequencing data.
Dondi A et al.
Biorxiv : the Preprint Server for Biology, 2024
38496441 (PubMed )
Supplement: media-4.xlsx › Feuille_1
Comprehensive genetic profiling and molecularly guided treatment for patients with primary CNS tumors.
Kuehn JC et al.
Npj Precision Oncology, 2024
39143272 (PubMed )
Supplement: 41698_2024_674_MOESM2_ESM.xlsx › Supplementary_Data_3
Description of longitudinal tumor evolution in a case of multiply relapsed clear cell sarcoma of the kidney.
Yaguchi T et al.
Cancer Reports (hoboken, N.j.), 2022
Mutational Profile and Potential Molecular Therapeutic Targets of Pheochromocytoma.
Ma X et al.
Frontiers in Endocrinology, 2022
[Detection of activating mutations in RAS/RAF/MEK/ERK and JAK/STAT signaling pathways].
Zarubina KI et al.
Terapevticheskii Arkhiv, 2020
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