Choo Z-N, Behr JM, Deshpande A, Hadi K, Yao X, Tian H, Takai K, Zakusilo G, Rosiene J, Paula ADa Cruz et al..  2023.  Most large structural variants in cancer genomes can be detected without long reads.. Nat Genet. 55(12):2139-2148.

Cohen LJ, Han S, Huang Y-H, Brady SF.  2018.  Identification of the Colicin V Bacteriocin Gene Cluster by Functional Screening of a Human Microbiome Metagenomic Library.. ACS Infect Dis. 4(1):27-32.

Calhoun SF, Reed J, Alexander N, Mason CE, Deitsch KW, Kirkman LA.  2017.  Chromosome End Repair and Genome Stability in .. MBio. 8(4)

Zhang Y, Yu J, Grachtchouk V, Qin T, Lumeng CN, Sartor MA, Koenig RJ.  2017.  Genomic binding of PAX8-PPARG fusion protein regulates cancer-related pathways and alters the immune landscape of thyroid cancer.. Oncotarget. 8(4):5761-5773.

Hosono N, Makishima H, Mahfouz R, Przychodzen B, Yoshida K, Jerez A, LaFramboise T, Polprasert C, Clemente MJ, Shiraishi Y et al..  2017.  Recurrent genetic defects on chromosome 5q in myeloid neoplasms.. Oncotarget. 8(4):6483-6495.

Han M-S, Kim J-N, Jeon E-O, Lee H-R, Koo B-S, Min K-C, Lee S-B, Bae Y-J, Mo J-S, Cho S-H et al..  2016.  The current epidemiological status of infectious coryza and efficacy of PoulShot Coryza in specific pathogen-free chickens.. J Vet Sci. 17(3):323-30.

D'Alessandro LCA, Turki SAl, Manickaraj AKumar, Manase D, Mulder BJM, Bergin L, Rosenberg HC, Mondal T, Gordon E, Lougheed J et al..  2016.  Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.. Genet Med. 18(2):189-98.

Henssen AG, Jiang E, Zhuang J, Pinello L, Socci ND, Koche R, Gönen M, Villasante CM, Armstrong SA, Bauer DE et al..  2016.  Forward genetic screen of human transposase genomic rearrangements.. BMC Genomics. 17:548.

Taur Y, Xavier JB, Lipuma L, Ubeda C, Goldberg J, Gobourne A, Lee YJoo, Dubin KA, Socci ND, Viale A et al..  2012.  Intestinal domination and the risk of bacteremia in patients undergoing allogeneic hematopoietic stem cell transplantation.. Clin Infect Dis. 55(7):905-14.

Oliveira TY, Resch W, Jankovic M, Casellas R, Nussenzweig MC, Klein IA.  2012.  Translocation capture sequencing: a method for high throughput mapping of chromosomal rearrangements.. J Immunol Methods. 375(1-2):176-81.

Worthey EA, Mayer AN, Syverson GD, Helbling D, Bonacci BB, Decker B, Serpe JM, Dasu T, Tschannen MR, Veith RL et al..  2011.  Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.. Genet Med. 13(3):255-62.

Mayer AN, Dimmock DP, Arca MJ, Bick DP, Verbsky JW, Worthey EA, Jacob HJ, Margolis DA.  2011.  A timely arrival for genomic medicine.. Genet Med. 13(3):195-6.