bioRxiv/medRxiv TRiP Review Activity

37 Reviews — EMBO Press — Bioinformatics

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Using deep mutational scanning data to benchmark computational phenotype predictors and identify pathogenic missense mutations
Livesey, B. J., Marsh, J. A.
10.1101/855957 — Posted: 2019-11-26 — Discussion: 2020-07-15  EMBO Press
Combinatorial prediction of gene-marker panels from single-cell transcriptomic data.
Delaney, C., Schnell, A., Cammarata, L., Yao-Smith, A., Regev, A., Kuchroo, V. K., Singer, M.
10.1101/655753 — Posted: 2019-05-30 — Discussion: 2019-11-26  EMBO Press
Detecting Novel Sequence Signals in Targeting Peptides Using Deep Learning
Almagro Armenteros, J. J., Salvatore, M., Winther, O., Emanuelsson, O., von Heijne, G., Elofsson, A., Nielsen, H.
10.1101/639203 — Posted: 2019-05-17 — Discussion: 2019-11-26  EMBO Press
Multi-Omics factor analysis disentangles heterogeneity in blood cancer
Argelaguet, R., Velten, B., Arnol, D., Dietrich, S., Zenz, T., Marioni, J. C., Buettner, F., Huber, W., Stegle, O.
10.1101/217554 — Posted: 2017-11-10 — Discussion: 2019-09-22  EMBO Press
The Landscape Of Human Mutually Exclusive Splicing
Hatje, K., Vidal, R., Rahman, R.-U., Simm, D., Hammesfahr, B., Shomroni, O., Kollmar, M., Bonn, S.
10.1101/133215 — Posted: 2017-05-02 — Discussion: 2019-09-22  EMBO Press
netDx: Patient classification using integrated patient similarity networks
Pai, S., Hui, S., Isserlin, R., Kaka, H., Bader, G.
10.1101/084418 — Posted: 2016-10-31 — Discussion: 2019-09-22  EMBO Press
A junction coverage compatibility score to quantify the reliability of transcript abundance estimates and annotation catalogs
Soneson, C., Love, M. I., Patro, R., Hussain, S., Malhotra, D., Robinson, M. D.
10.1101/378539 — Posted: 2018-07-28 — Discussion: 2019-09-22  EMBO Press

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