Channel: Vanderbilt University

This collection includes bioRxiv and medRxiv papers from authors at Vanderbilt University.

2602 Articles

Proofreading-deficient coronaviruses adapt over long-term passage for increased fidelity and fitness without reversion of exoribonuclease-inactivating mutations

Graepel, K., Lu, X., Case, J. B., Sexton, N. R., Smith, E. C., Denison, M. R.

10.1101/175562 — Posted: 2017-08-11

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

PGC Bipolar Disorder/Schizophrenia Working Group, , Ruderfer, D., Sklar, P., Kendler, K.

10.1101/173435 — Posted: 2017-08-08

Quartet-based computations of internode certainty provide accurate and robust measures of phylogenetic incongruence

Zhou, X., Lutteropp, S., Czech, L., Stamatakis, A., von Looz, M., Rokas, A.

10.1101/168526 — Posted: 2017-07-27

Whole genome bisulfite sequencing reveals a sparse, but robust pattern of DNA methylation in the Dictyostelium discoideum genome

Steenwyk, J., St. Denis, J., Dresch, J., Larochelle, D., Drewell, R.

10.1101/166033 — Posted: 2017-07-20

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

- International Multiple Sclerosis Genetics Consorti, , Patsopoulos, N., Baranzini, S. E., Santaniello, A., Shoostari, P., Cotsapas, C., Wong, G., Beecham, A. H., James, T., Replogle, J., Vlachos, I., McCabe, C., Pers, T., Brandes, A., White, C., Keenan, B., Cimpean, M., Winn, P., Panteliadis, I.-P., Robbins, A., Andlauer, T. F. M., Zarzycki, O., Dubois, B., Goris, A., Bach Sondergaard, H., Sellebjerg, F., Soelberg Sorensen, P., Ullum, H., Wegner Thoerner, L., Saarela, J., Cournu-Rebeix, I., Damotte, V., Fontaine, B., Guillot-Noel, L., Lathrop, M., Vukusik, S., Berthele, A., Biberacher, V., B

10.1101/143933 — Posted: 2017-07-13

FUCCI tracking shows that Neurog3 levels vary with cell-cycle phase in endocrine-biased pancreatic progenitors

Bechard, M. E., Bankaitis, E. D., Ustione, A., Piston, D., Magnuson, M. A., Wright, C. V. E.

10.1101/153700 — Posted: 2017-06-21

Amyloid accumulation drives proteome-wide alterations in mouse models of Alzheimers disease like pathology

Savas, J. N., Wang, Y.-Z., DeNardo, L. A., Martinez-Bartolome, S., McClatchy, D. B., Hark, T. J., Shanks, N. F., Cozzolino, K. A., Lavallee-Adam, M., Smukowski, S. N., Park, S. K., Kelly, J. W., Koo, E. H., Nakagawa, T., Masliah, E., Ghosh, A., Yates, J. R.

10.1101/150623 — Posted: 2017-06-15

Genome-wide association study of Alcohol Use Disorder Identification Test (AUDIT) scores in 20,328 research participants of European ancestry

Sanchez-Roige, S., Fontanillas, P., Elson, S. L., - the 23andMe Research Team, , Gray, J. C., de Wit, H., Davis, L. K., MacKillop, J., Palmer, A. A.

10.1101/147397 — Posted: 2017-06-15

SNP-based heritability estimation: measurement noise, population stratification, and stability

Gamazon, E. R., Park, D. S.

10.1101/040055 — Posted: 2017-06-13

Harmonization of cortical thickness measurements across scanners and sites

Fortin, J.-P., Cullen, N., Sheline, Y. I., Taylor, W. D., Aselcioglu, I., Adams, P., Cooper, C., Fava, M., McGrath, P. J., McInnis, M., Parsey, R. V., Phillips, M. L., Trivedi, M. H., Weissman, M. M., Shinohara, R. T.

10.1101/148502 — Posted: 2017-06-10

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