Author

Dacian Reece-Stremtan

George Washington University

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

Biology Disciplines

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Bioinformatics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Anélia HorvathiD· 2 shared Helen IbeawuchiiD· 2 shared Hongyu LiuiD· 2 shared Justin Sein· 2 shared Liam Flinn SpurriD· 2 shared N. M. PrashantiD· 2 shared Nawaf AlomraniD· 2 shared Pavlos BousounisiD· 2 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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2 shared papersGenomics

Anélia HorvathORCID

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2 papers

Recent·Most cited

Estimating allele-specific expression of SNVs from 10x Genomics Single-Cell RNA-Sequencing Data

N. M. Prashant, Hongyu Liu, Pavlos Bousounis, Liam Flinn Spurr, Nawaf Alomran, Helen Ibeawuchi, Justin Sein, Dacian Reece-Stremtan, Anélia Horvath

The paper estimates allele-specific expression from 10x Genomics scRNA-seq data and finds that most SNVs are bi-allelic at higher read thresholds, with intronic SNVs showing more monoallelic expression.

Genes · Feb 25, 2020Peer-reviewedGenomics

RsQTL: correlation of expressed SNVs with splicing using RNA-sequencing data

Justin Sein, Liam Flinn Spurr, Pavlos Bousounis, N. M. Prashant, Hongyu Liu, Nawaf Alomran, Jimmy Bernot, Helen Ibeawuchi, Dacian Reece-Stremtan, Anélia Horvath

RsQTL identifies splicing quantitative trait loci by correlating variant allele fractions with splicing patterns in RNA-seq data from human tissues.

bioRxiv · Nov 17, 2019 · PreprintBioinformatics