Author

Marco Crotti

University of CambridgeORCID 0000-0002-8619-7988Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:genome assembly· 1 Organism:human· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Alison M. DunningiD· 1 shared Anders KvistiD· 1 shared Andreas HadjisavvasiD· 1 shared Anna González‐NeiraiD· 1 shared Arnaud DroitiD· 1 shared Audrey Y. JungiD· 1 shared Belén Herráez· 1 shared Caroline Baynes· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 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 paperGenetic & Genomic Medicine

Alison M. DunningORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJun 17, 2022

Exome sequencing identifies novel susceptibility genes and defines the contribution of coding variants to breast cancer risk.

Naomi Wilcox, Martine Dumont, Anna González‐Neira…·Jacques Simard

The paper uses whole-exome sequencing data to identify novel breast cancer susceptibility genes and assess the contribution of coding variants to breast cancer risk.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky

GenomicsMethods in Ecology and EvolutionPeer-reviewedApr 9, 2020

Population genomic SNPs from epigenetic RADs: gaining genetic and epigenetic data from a single established next-generation sequencing approach

Marco Crotti, Colin E. Adams, Kathryn R. Elmer

This paper shows that epiRADseq can generate SNPs comparable to ddRADseq for population genomic analyses, reducing costs and enabling combined genetic and epigenetic studies.

12 citations

DNA methylationwhole-genome sequencing

𝕏 PostBluesky