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Items: 8


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

Shih SY, Bose N, Gonçalves ABR, Erlich HA, Calloway CD.

Genes (Basel). 2018 Jan 22;9(1). pii: E49. doi: 10.3390/genes9010049. Erratum in: Genes (Basel). 2018 Feb 14;9(2):.


A phylogenetic approach for haplotype analysis of sequence data from complex mitochondrial mixtures.

Vohr SH, Gordon R, Eizenga JM, Erlich HA, Calloway CD, Green RE.

Forensic Sci Int Genet. 2017 Sep;30:93-105. doi: 10.1016/j.fsigen.2017.05.007. Epub 2017 May 29.


A twin study of mitochondrial DNA polymorphisms shows that heteroplasmy at multiple sites is associated with mtDNA variant 16093 but not with zygosity.

Andrew T, Calloway CD, Stuart S, Lee SH, Gill R, Clement G, Chowienczyk P, Spector TD, Valdes AM.

PLoS One. 2011;6(8):e22332. doi: 10.1371/journal.pone.0022332. Epub 2011 Aug 3.


DNA sequencing by MALDI-TOF MS using alkali cleavage of RNA/DNA chimeras.

Mauger F, Bauer K, Calloway CD, Semhoun J, Nishimoto T, Myers TW, Gelfand DH, Gut IG.

Nucleic Acids Res. 2007;35(8):e62. Epub 2007 Apr 10.


Mitochondrial DNA typing screens with control region and coding region SNPs.

Kline MC, Vallone PM, Redman JW, Duewer DL, Calloway CD, Butler JM.

J Forensic Sci. 2005 Mar;50(2):377-85.


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