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When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants

MOTIVATION: Loss-of-function genetic variants are frequently associated with severe clinical phenotypes, yet many are present in the genomes of healthy individuals. The available methods to assess the impact of these variants rely primarily upon evolutionary conservation with little to no considerat...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Bioinformatics
Κύριοι συγγραφείς: Pagel, Kymberleigh A, Pejaver, Vikas, Lin, Guan Ning, Nam, Hyun-Jun, Mort, Matthew, Cooper, David N, Sebat, Jonathan, Iakoucheva, Lilia M, Mooney, Sean D, Radivojac, Predrag
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Oxford University Press 2017
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5870554/
https://ncbi.nlm.nih.gov/pubmed/28882004
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx272
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