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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 2011 Aug 12;89(2):345. doi: 10.1016/j.ajhg.2011.07.008

Using VAAST to Identify an X-linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency

Alan F Rope, Kai Wang, Rune Evjenth, Jinchuan Xing, Jennifer J Johnston, Jeffrey J Swensen, W Evan Johnson, Barry Moore, Chad D Huff, Lynne M Bird, John C Carey, John M Opitz, Cathy A Stevens, Tao Jiang, Christa Schank, Heidi Deborah Fain, Reid Robison, Brian Dalley, Steven Chin, Sarah T South, Theodore J Pysher, Lynn B Jorde, Hakon Hakonarson, Johan R Lillehaug, Leslie G Biesecker, Mark Yandell, Thomas Arnesen, Gholson J Lyon
PMCID: PMC3155194

(The American Journal of Human Genetics 89, 28–43; July 15, 2011)

In the original version of this article, the citations in the following sentences were incorrect. The citations should have been listed as follows. The authors regret these errors.

“Burroughs Wheeler alignment (BWA)1 version 0.5.8 was used to align the sequencing reads, and the default parameters were used for fragment reads, to the human genome sequence build 36 downloaded from the UCSC Genome Browser or the 1000 Genomes Project websites.12 Alignments were converted from SAM format to sorted, indexed BAM files with SamTools.2

References

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