Author

Evan E. Eichler

Primary ORCID profile (0000-0002-8246-4014 · 139 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Evan E. EichleriD139 papers · Howard Hughes Medical Institute

Biology Disciplines

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Bioinformatics· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:whole-genome sequencing· 2 Approach:experimental assay· 1 Research Focus:genome assembly· 1 Research Focus:imputation· 1 Approach:statistical model· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Abdel Abdellaoui· 1 shared Alexander Schöenhuth· 1 shared Amy Ly· 1 shared André G. Uitterlinden· 1 shared Archana Raja· 1 shared Bradley P. Coe· 1 shared Carl Baker· 1 shared Chad Tomlinson· 1 shared

Activity by Year

2016-2016 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetics

Abdel Abdellaoui

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2 papers

Recent·Most cited

High-Quality Assembly of an Individual of Yoruban Descent

Karyn Meltz Steinberg, Tina Graves Lindsay, Valerie A. Schneider, Mark J.P. Chaisson, Chad Tomlinson, John Huddleston, Patrick Minx, Milinn Kremitzki, Derek Albrecht, Vincent Magrini, Sean McGrath, Archana Raja, Carl Baker, Lana Harshman, LaDeana W. Hillier, , Richard K. Wilson

This paper presents a high-quality de novo assembly of a Yoruban individual using multiple sequencing technologies and demonstrates the utility of diploid assembly in improving genome quality.

bioRxiv · Aug 2, 2016 · PreprintBioinformatics

A high-quality reference panel reveals the complexity and distribution of structural genome changes in a human population

Jayne Y. Hehir-Kwa, Tobias Marschall, Wigard P. Kloosterman, Laurent C. Francioli, Jasmijn A. Baaijens, Louis J. Dijkstra, Abdel Abdellaoui, Vyacheslav Koval, Djie Tjwan Thung, René Wardenaar, Ivo Renkens, Bradley P. Coe, Patrick Deelen, Joep de Ligt, Eric-Wubbo Lameijer, , Victor Guryev

This study creates a high-quality reference panel of structural variants from 769 Dutch individuals, revealing new variants and their linkage to known SNPs, improving imputation accuracy for genome-wide association studies.

bioRxiv · Jul 2, 2016 · PreprintGenetics