Author

Moises A. Serrano

BioNano Genomics (United States)ORCID 0000-0002-1037-9304Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Assay:whole-genome sequencing· 3 Approach:statistical model· 2 Research Focus:benchmarking· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Megan M. MartiniD· 2 shared Rena J. VanzoiD· 2 shared Alex R. HastieiD· 1 shared Alka ChaubeyiD· 1 shared Andy P. Peiffer· 1 shared Andy Wing Chun PangiD· 1 shared Ben Clifford· 1 shared Brynn LevyiD· 1 shared

Activity by Year

2017-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 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 papersGenomics

Megan M. MartinORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJan 21, 2023

Comparative benchmarking of optical genome mapping and chromosomal microarray reveals high technological concordance in CNV identification and structural variant refinement

Hayk Barseghyan, Andy Wing Chun Pang, Ben Clifford…·Alex R. Hastie

This study compares optical genome mapping (OGM) and chromosomal microarray (CMA) for detecting copy number variants and structural variants, finding high concordance and additional structural insights from OGM.

5 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsbioRxivPreprintFeb 4, 2021

NeuroSCORE: A Genome-wide Omics-Based Model to Identify Candidate Disease Genes of the Central Nervous System

Kyle Davis, Colleen G. Bilancia, Megan M. Martin…·Moises A. Serrano

NeuroSCORE scores 19,598 genes based on five CNS-related metrics, identifying 1,580 high-scoring genes significantly associated with CNS phenotypes.

DOI 10.1101/2021.02.04.429640

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsPLoS CurrentsPeer-reviewedJan 1, 2017

Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions

Charles H. Hensel, Rena J. Vanzo, Megan M. Martin…·Edward Robert Wassman

This paper validates the analytical and clinical utility of FirstStepDx PLUS, a chromosomal microarray optimized for neurodevelopmental conditions, showing its effectiveness in detecting copy number variants using buccal and blood samples.

11 citations

humanwhole-genome sequencing

𝕏 PostBluesky