SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes. | Bioinformatics;34(10): 1774-1777, 2018 05 15. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Advanced Search EVID@Easy

SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes.

Antaki, Danny; Brandler, William M; Sebat, Jonathan.

Affiliation

Antaki D; Beyster Center for Genomics of Psychiatric Diseases.
Brandler WM; Department of Psychiatry.
Sebat J; Department of Cellular and Molecular Medicine and Pediatrics.

Bioinformatics ; 34(10): 1774-1777, 2018 05 15.

Article in En | MEDLINE | ID: mdl-29300834

Subject(s)

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Human / Mutation Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Bioinformatics Journal subject: INFORMATICA MEDICA Year: 2018 Document type: Article Country of publication: Reino Unido

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome, Human / Mutation Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Bioinformatics Journal subject: INFORMATICA MEDICA Year: 2018 Document type: Article Country of publication: Reino Unido