Author

C. Gawad

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

Bioengineering· 1 Cancer Biology· 1 Evolutionary Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:whole-genome sequencing· 3 Research Focus:clustering· 2 Approach:experimental assay· 2 Research Focus:variant calling· 2 Research Focus:cell type annotation· 1 Approach:deep learning· 1 Research Focus:differential expression· 1

Frequent Co-Authors

A. R. D'Avino· 1 shared B. Behr· 1 shared C. Potenski· 1 shared D. A. Landau· 1 shared D. Klein· 1 shared D. Yergeau· 1 shared J. Easton· 1 shared J. Luquette· 1 shared

Activity by Year

2017-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 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

1 shared paperEvolutionary Biology

A. R. D'Avino

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Defining ancestry, heritability and plasticity of cellular phenotypes in somatic evolution

J. S. Schiffman, A. R. D'Avino, T. Prieto, Y. Pang, Y. Fan, S. Rajagopalan, C. Potenski, T. Hara, M. L. Suva, C. Gawad, D. A. Landau

The paper introduces PATH, a framework to quantify heritability and plasticity of cellular phenotypes in somatic evolution using single-cell data from mouse and human samples.

Nature Genetics · Sep 24, 2024Peer-reviewedEvolutionary Biology

Genome-wide Disease Screening in Early Human Embryos with Primary Template-Directed Amplification

Y. Xia, V. Gonzales-Pena, D. Klein, J. Luquette, L. Puzon, N. Siddiqui, V. Reddy, P. Park, B. Behr, C. Gawad

This paper introduces a method to screen early human embryos for genetic variants using primary template-directed amplification, identifying aneuploidy, mitochondrial variants, and disease-causing mutations, and computing polygenic risk scores.

bioRxiv · Jul 6, 2021 · PreprintBioengineering

Genome-wide Segregation of Single Nucleotide and Structural Variants into Single Leukemia Cells

J. Easton, V. Gonzalez-Pena, D. Yergeau, X. Ma, C. Gawad

The paper introduces a method to analyze single-cell variants in leukemia, finding structural variations precede single nucleotide changes in cancer development.

BMC Genomics · Nov 25, 2017Peer-reviewedCancer Biology