Search

Your search keyword '"Daniel Hübschmann"' showing total 44 results

Search Constraints

Start Over You searched for: Author "Daniel Hübschmann" Remove constraint Author: "Daniel Hübschmann" Language english Remove constraint Language: english
44 results on '"Daniel Hübschmann"'

Search Results

1. Translational and clinical comparison of whole genome and transcriptome to panel sequencing in precision oncology

2. Multiple myeloma long-term survivors exhibit sustained immune alterations decades after first-line therapy

3. Molecular Characterization and Clinical Relevance of MGMT‐Silenced Pancreatic Cancer

4. Multi-omic and functional analysis for classification and treatment of sarcomas with FUS-TFCP2 or EWSR1-TFCP2 fusions

5. An AI-based segmentation and analysis pipeline for high-field MR monitoring of cerebral organoids

6. NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology

7. Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling

8. simplifyEnrichment: A Bioconductor Package for Clustering and Visualizing Functional Enrichment Results

9. aRgus: Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment

11. P1218: A REPROGRAMMING OF THE LYMPH NODE MICROENVIRONMENT UNDERLIES LOSS OF COMPARTMENTALISATION IN AGGRESSIVE LYMPHOMAS

12. PB1759: RETAINED FUNCTIONAL NORMAL AND/OR PRE-LEUKEMIC HSCS IN THE BONE MARROW ARE ASSOCIATED TO GOOD PROGNOSIS IN DNMT3AMUTNPM1MUT AML PATIENTS

13. Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity

14. MGMT inactivation as a new biomarker in patients with advanced biliary tract cancers

15. The genomic and transcriptional landscape of primary central nervous system lymphoma

16. Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines

17. Comparison of extraction methods for intracellular metabolomics of human tissues

18. Framework for quality assessment of whole genome cancer sequences

19. The landscape of chromothripsis across adult cancer types

20. Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

21. Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma

22. Case Report: Abdominal Lymph Node Metastases of Parathyroid Carcinoma: Diagnostic Workup, Molecular Diagnosis, and Clinical Management

23. Genomic features of renal cell carcinoma with venous tumor thrombus

24. Integrative genomic and transcriptomic analysis of leiomyosarcoma

25. Spatial niche formation but not malignant progression is a driving force for intratumoural heterogeneity

26. Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers

27. cola: an R/Bioconductor package for consensus partitioning through a general framework

28. Detection of Structural Variants in Circulating Cell-Free DNA from Sarcoma Patients Using Next Generation Sequencing

29. Genomic features of renal cell carcinoma with venous tumor thrombus

30. Analysis of mutational signatures with yet another package for signature analysis

31. ShinyButchR: interactive NMF-based decomposition workflow of genome-scale datasets

32. Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

33. Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

34. The whole-genome landscape of medulloblastoma subtypes

35. Evaluation of whole genome sequencing data

36. Response to olaparib in a PALB2 germline mutated prostate cancer and genetic events associated with resistance

37. The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma

38. Author Correction : The landscape of genomic alterations across childhood cancers

39. IG-MYC+ neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomas

40. Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature

41. Newborn screening for severe combined immunodeficiency using a novel and simplified method to measure T-cell excision circles (TREC)

42. ACEseq – allele specific copy number estimation from whole genome sequencing

43. Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas

44. Single-cell proteo-genomic reference maps of the hematopoietic system enable the purification and massive profiling of precisely defined cell states

Catalog

Books, media, physical & digital resources