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Items: 4

1.

Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.

Clark MM, Hildreth A, Batalov S, Ding Y, Chowdhury S, Watkins K, Ellsworth K, Camp B, Kint CI, Yacoubian C, Farnaes L, Bainbridge MN, Beebe C, Braun JJA, Bray M, Carroll J, Cakici JA, Caylor SA, Clarke C, Creed MP, Friedman J, Frith A, Gain R, Gaughran M, George S, Gilmer S, Gleeson J, Gore J, Grunenwald H, Hovey RL, Janes ML, Lin K, McDonagh PD, McBride K, Mulrooney P, Nahas S, Oh D, Oriol A, Puckett L, Rady Z, Reese MG, Ryu J, Salz L, Sanford E, Stewart L, Sweeney N, Tokita M, Van Der Kraan L, White S, Wigby K, Williams B, Wong T, Wright MS, Yamada C, Schols P, Reynders J, Hall K, Dimmock D, Veeraraghavan N, Defay T, Kingsmore SF.

Sci Transl Med. 2019 Apr 24;11(489). pii: eaat6177. doi: 10.1126/scitranslmed.aat6177.

PMID:
31019026
2.

Multiple sequence information for threading algorithms.

Defay TR, Cohen FE.

J Mol Biol. 1996 Sep 20;262(2):314-23.

PMID:
8831796
3.

Evaluation of current techniques for ab initio protein structure prediction.

Defay T, Cohen FE.

Proteins. 1995 Nov;23(3):431-45.

PMID:
8710836
4.

Proposed structure of the A domains of factor VIII by homology modelling.

Pan Y, DeFay T, Gitschier J, Cohen FE.

Nat Struct Biol. 1995 Sep;2(9):740-4.

PMID:
7552743

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