Join us for a special in-person seminar where we explore how single-cell DNA multiomics help unveiling cellular complexity.
Quantitative characterization of genotype and phenotype at the single-cell level reveals clonal phylogeny and selection at higher resolution, ultimately improving personalized therapeutic selection. By identifying SNVs, CNVs, and surface protein changes and revealing co-occurrence and zygosity of mutations in single cells, Tapestri enables comprehensive insights into disease progression, development of therapy resistance, and MRD.
Our invited speakers will present data from different areas of research like acute myeloid leukemia (AML), single-cell MRD in AML, functional phenotyping of genomic variants using multiomic scDNA-scRNA-seq, single-cell DNA seq assay for reconstructing the clonal evolution of tumors from FFPE samples, targeted single-cell DNA methylation (scTAM-seq), single-cell Multiple Myeloma multiomics and genome editing.
In-between the presentations we would like to invite you for food, drinks and networking.
Please have a look at the agenda here
Location: Konferenzraum K1 & K2, Im Neuenheimer Feld 280, 69120 Heidelberg
Time: 9.30 - 15.00h
If you are unable to attend in-person but would still like to hear our amazing speakers, you can register to attend virtually via Zoom here.
Speakers
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| Martina Braun, PhD Centre for Genomic Regulation (CRG) |
Dominik Lindenhofer, PhD European Molecular Biology Laboratory (EMBL) |
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| Enise Ceran, MD, PhD University Hospital Heidelberg |
Darja Karpova, PhD DRK Blutspendedienst |
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| Wout Megchelenbrink, PhD The Princess Máxima Center |
Daniela Hirsch, MD, PhD University of Regensburg |
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| Celine Mazzotti Centre de Recherches en Cancérologie de Toulouse (Oncopole) |
Gema Fuerte, MSc Mission Bio |
