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Author/Creator Sulovari, Arvis

3. Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads. (11th November 2019)

Authors:
Vollger, Mitchell R.; Logsdon, Glennis A.; Audano, Peter A.; Sulovari, Arvis; Porubsky, David; Peluso, Paul; Wenger, Aaron M.; Concepcion, Gregory T.; Kronenberg, Zev N.; Munson, Katherine M.; Baker, Carl; Sanders, Ashley D.; Spierings, Diana C.J.; Lansdorp, Peter M.; Surti, Urvashi; Hunkapiller,...
Journal:
Annals of human genetics
Issue:
Volume 84:Number 2(2020:Mar.)
Page Start:
125
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity. (January 2019)

Authors:
Coe, Bradley; Stessman, Holly; Sulovari, Arvis; Geisheker, Madeleine; Bakken, Trygve; Lake, Allison; Dougherty, Joseph; Lein, Ed; Hormozdiari, Fereydoun; Bernier, Raphael; Eichler, Evan
Journal:
Nature genetics
Issue:
Volume 51:Number 1(2019)
Page Start:
106
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗