The PeopleSeq Consortium – Genomes2People

Genomic sequencing is available to and being utilized by physicians and their patients in both research and clinical settings. Instead of using genomic technology in the hopes of identifying a cause for a specific condition, genomic sequencing in healthy individuals would follow a model of “predispositional” genomic testing. This model envisions results being returned in a … Continued

Publications

2026

Elective genomic sequencing for adults in research, clinical and commercial contexts

Linderman MD, Adelson SM, Berro TM, Anderson JL, Crawford SD, Cunningham TJ, Esplin ED, Ewing-Crawford AT, Nielsen DE, Pereira S, Schmidlen T, Andrighetti H, Bleyl SB, Church GM, Haverfield EV, Hegde M, Konstantinos LN, Kruszka P, Leonard D, May T, McGinniss M, Pandya V, Schadt EE, Tzovaras BG, Zettler B, McGuire AL, Green RC and the PeopleSeq Study Team

BMC Medical Genomics In Press

2021

A framework for automated gene selection in genomic sequencing

Lazo de la Vega L, Yu W, Machini K, Austin-Tse CA, Hao L, Blout Zawatsky CL, Mason-Suares H, Green RC, Rehm HL, Lebo MS

Genetics in Medicine | PMID: 34113001 Jun 2021

Development and validation of a comprehensive genomics knowledge scale

Linderman MD, Suckiel SA, Thompson N, Weiss DJ, Roberts JS, Green RC

Public Health Genomics May 2021

2019

Predispositional genome sequencing in healthy adults: Design, participant characteristics, and early outcomes of the PeopleSeq Consortium

Zoltick ES, Linderman MD, McGinniss MA, Ramos E, Ball MP, Church GM, Leonard DGB, Pereira S, McGuire AL, Caskey T, Sanderson SC, Schadt EE, Nielsen DE, Crawford SC, Green RC

Genome Medicine Feb 2019