Author

Marzieh Eslami Rasekh

Boston UniversityORCID 0000-0003-0046-158XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Bioinformatics· 3

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Can AlkaniD· 2 shared Camir RickettsiD· 1 shared Chris T Amemiya· 1 shared Evan E. EichleriD· 1 shared Ezgi EbreniD· 1 shared Fatih KaraoğlanoğluiD· 1 shared Francesca AntonacciiD· 1 shared Gary BensoniD· 1 shared

Activity by Year

2017-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersBioinformatics

Can AlkanORCID

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3 papers

Recent·Most cited

BioinformaticsNucleic Acids ResearchPeer-reviewedMar 18, 2021

Genome-wide characterization of human minisatellite VNTRs: population-specific alleles and gene expression differences

Marzieh Eslami Rasekh, Yozen A. Hernandez, Samantha D. Drinan…·Gary Benson

The paper characterizes human minisatellite VNTRs, identifies population-specific alleles, and links some VNTRs to gene expression differences.

37 citations

humanwhole-genome sequencing

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BioinformaticsGenome biologyPeer-reviewedMar 19, 2020

Characterization of segmental duplications and large inversions using Linked-Reads

Fatih Karaoğlanoğlu, Camir Ricketts, Marzieh Eslami Rasekh…·Can Alkan

The paper introduces VALOR2, a new software package that uses Linked-Read sequencing to detect large genomic inversions and characterize interspersed segmental duplications.

21 citations

humanlong-read sequencing

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BioinformaticsBMC GenomicsPeer-reviewedDec 1, 2017

Discovery of large genomic inversions using pooled clone sequencing

Marzieh Eslami Rasekh, Giorgia Chiatante, Mattia Miroballo…·Can Alkan

The paper introduces dipSeq, an algorithm for discovering large genomic inversions using pooled clone sequencing, validated on simulated and real data.

DOI 10.1186/s12864-016-3444-1

humanwhole-genome sequencing

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