Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples.

Shih, Shelly Y; Bose, Nikhil; Gonçalves, Anna Beatriz R; Erlich, Henry A; Calloway, Cassandra D

Shih, Shelly Y; Bose, Nikhil; Gonçalves, Anna Beatriz R; Erlich, Henry A; Calloway, Cassandra D.

Afiliación

Shih SY; Children's Hospital Oakland Research Institute, 5700 Martin Luther King Jr. Way, Oakland, CA 94609, USA. sshih@chori.org.
Bose N; Children's Hospital Oakland Research Institute, 5700 Martin Luther King Jr. Way, Oakland, CA 94609, USA. nbose@ucdavis.edu.
Gonçalves ABR; Forensic Science Graduate Program, University of California, Davis, 1909 Galileo Ct. Ste. B, Davis, CA 95618, USA. nbose@ucdavis.edu.
Erlich HA; Children's Hospital Oakland Research Institute, 5700 Martin Luther King Jr. Way, Oakland, CA 94609, USA. gonannab@gmail.com.
Calloway CD; Laboratório de Diagnósticos por DNA (LDD), Universidade do Estado do Rio de Janeiro (UERJ), Instituto de Biologia Roberto Alcantara Gomes (IBRAG), Rua São Francisco Xavier, number 524, Pavilhão Haroldo Lisboa da Cunha, 20550-900 Rio de Janeiro, RJ, Brazil. gonannab@gmail.com.

Genes (Basel) ; 9(1)2018 Jan 22.

Article en En | MEDLINE | ID: mdl-29361782

Palabras clave

Forensic Genetics; Massively Parallel Sequencing (MPS); Next Generation Sequencing (NGS); Probe Capture Target Enrichment; Single Nucleotide Polymorphism (SNP); degraded DNA; mitochondrial DNA (mtDNA)

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Genes (Basel) Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

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