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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Article
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados