Author

M. Valecha

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Cancer Biology· 1 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 2 Approach:statistical model· 2 Research Focus:clustering· 1 Approach:deep learning· 1 Research Focus:differential expression· 1 Assay:scRNA-seq· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

D. Posada· 2 shared H. Ogilvie· 1 shared H. Zafar· 1 shared J. Kuipers· 1 shared L. Nakhleh· 1 shared M. Edrisi· 1 shared N. Beerenwinkel· 1 shared N. Borgsmüller· 1 shared

Activity by Year

2022-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersEvolutionary Biology

D. Posada

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Single-cell phylogenies reveal deviations from clock-like, neutral evolution in cancer and healthy tissues

N. Borgsmüller, M. Valecha, J. Kuipers, N. Beerenwinkel, D. Posada

This study uses single-cell DNA sequencing to test for neutral evolution in cancer and healthy tissues, finding deviations from a clock-like model in many datasets.

bioRxiv · Aug 9, 2022 · PreprintEvolutionary Biology

Phylovar: Towards scalable phylogeny-aware inference of single-nucleotide variations from single-cell DNA sequencing data

M. Edrisi, M. Valecha, S. Chowdary, S. Robledo, H. Ogilvie, D. Posada, H. Zafar, L. Nakhleh

Phylovar improves scalability and accuracy of SNV detection in scDNAseq data by leveraging phylogenetic information, outperforming existing methods in speed and precision.

bioRxiv · Jan 16, 2022 · PreprintCancer Biology