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From prioritisation to understanding: mechanistic predictions of variant effects

Abstract The widespread application of sequencing technologies, used for example to obtain data from healthy individuals or patient cohorts, has led to the identification of numerous mutations, the effect of which remains largely unclear. Therefore, developing approaches allowing accurate in‐silico...

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Bibliographic Details
Main Authors: Greg Slodkowicz, M Madan Babu
Format: Artigo
Language:Inglês
Published: Springer Nature 2018-12-01
Series:Molecular Systems Biology
Online Access:https://doi.org/10.15252/msb.20188741
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