Sergey Batalov
7PUBLICATIONS
45CO-AUTHORS
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Publications (7)
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|Feb 14, 2023
Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots.Yan Ding, Mallory Owen, Jennie Le
|Jul 26, 2022
An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases.Mallory J Owen, Sebastien Lefebvre, Christian Hansen
|May 27, 2021
Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|May 27, 2021
Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|Apr 23, 2021
Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.Nathaly M Sweeney, Shareef A Nahas, Shimul Chowdhury
|Aug 22, 2020
Partially automated whole-genome sequencing reanalysis of previously undiagnosed pediatric patients can efficiently yield new diagnoses.Kiely N James, Michelle M Clark, Brandon Camp
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Frequent Collaborators
5 joint publications
Narayanan Veeraraghavan
5 joint publications
Stephen F Kingsmore
5 joint publications
David P Dimmock
4 joint publications
Michelle M Clark
3 joint publications
Julie Cakici
3 joint publications
Nathaly M Sweeney
2 joint publications
Kevin P Hall
2 joint publications
John Reynders
2 joint publications
Sheldon Gilmer
1 joint publications
Rebecca J Baer
