Literature DB >> 29910094

Validation of the diagnostic potential of mtDNA copy number derived from whole genome sequencing.

Rachel Brockhage1, Jesse Slone1, Zeqiang Ma2, Madhuri R Hegde3, C Alexander Valencia4, Taosheng Huang5.   

Abstract

Year:  2018        PMID： 29910094     DOI： 10.1016/j.jgg.2018.06.001

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN： 1673-8527            Impact factor:   4.275


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  2 in total

1.  Reply to Lutz-Bonengel et al.: Biparental mtDNA transmission is unlikely to be the result of nuclear mitochondrial DNA segments.

Authors:  Shiyu Luo; C Alexander Valencia; Jinglan Zhang; Ni-Chung Lee; Jesse Slone; Baoheng Gui; Xinjian Wang; Zhuo Li; Sarah Dell; Jenice Brown; Stella Maris Chen; Yin-Hsiu Chien; Wuh-Liang Hwu; Pi-Chuan Fan; Lee-Jun Wong; Paldeep S Atwal; Taosheng Huang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-01-23       Impact factor: 11.205

2.  Validation of low-coverage whole-genome sequencing for mitochondrial DNA variants suggests mitochondrial DNA as a genetic cause of preterm birth.

Authors:  Zeyu Yang; Jesse Slone; Xinjian Wang; Jack Zhan; Yongbo Huang; Bahram Namjou; Kenneth M Kaufman; Michael Pauciulo; John B Harley; Louis J Muglia; Iouri Chepelev; Taosheng Huang
Journal:  Hum Mutat       Date:  2021-09-08       Impact factor: 4.700
  2 in total

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