Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing

Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing

Bibliographic Details
Main Author: Baird, Denis Andrew
Published: University of Bristol 2017
Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.723503
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spelling ndltd-bl.uk-oai-ethos.bl.uk-7235032017-11-03T03:19:34ZStatistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencingBaird, Denis Andrew2017University of Bristolhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.723503Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
author Baird, Denis Andrew
spellingShingle Baird, Denis Andrew
Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
author_facet Baird, Denis Andrew
author_sort Baird, Denis Andrew
title Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
title_short Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
title_full Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
title_fullStr Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
title_full_unstemmed Statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
title_sort statistical and bioinformatics approaches for discovering pathogenic single nucleotide variants in idiopathic early on-set nephrotic syndrome using exome sequencing
publisher University of Bristol
publishDate 2017
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.723503
work_keys_str_mv AT bairddenisandrew statisticalandbioinformaticsapproachesfordiscoveringpathogenicsinglenucleotidevariantsinidiopathicearlyonsetnephroticsyndromeusingexomesequencing
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