Single Nucleotide Variant Counts Computed from RNA Sequencing and Cellular Traffic into Human Kidney Allografts

Advances in bioinformatics allow identification of single nucleotide polymorphisms (variants) from RNA sequence data. In an allograft biopsy, two genomes contribute to the RNA pool, one from the donor organ and the other from infiltrating recipient’s cells. We hypothesize that imbalances in genetic...

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Bibliografiske detaljer
Udgivet i:Am J Transplant
Main Authors: Thareja, Gaurav, Yang, Hua, Hayat, Shahina, Mueller, Franco B., Lee, John R., Lubetzky, Michelle, Dadhania, Darshana M., Belkadi, Aziz, Seshan, Surya V., Suhre, Karsten, Suthanthiran, Manikkam, Muthukumar, Thangamani
Format: Artigo
Sprog:Inglês
Udgivet: 2018
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6160347/
https://ncbi.nlm.nih.gov/pubmed/29659169
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ajt.14870
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