Clinical Applications of Next-Generation Sequencing: The 2013 Human Genome Variation Society Scientific Meeting-Reference-Cited by-同舟云学术

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Clinical Applications of Next-Generation Sequencing: The 2013 Human Genome Variation Society Scientific Meeting

Published:2013-09-04 Issue:11 Volume:34 Page:1583-1587
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Ellard Sian¹,Patrinos George P.²,Oetting William S.³

Affiliation:

1. University of Exeter Medical School; Exeter United Kingdom

2. Department of Pharmacy; School of Health Sciences; University of Patras; Patras Greece

3. Department of Experimental and Clinical Pharmacology; University of Minnesota; Minneapolis Minnesota

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22400/fullpdf

Reference6 articles.

1. Computational science. Troubling trends in scientific software use;Joppa;Science,2013

2. Prediction of mutant mRNA splice isoforms by information theory-based exon definition;Mucaki;Hum Mutat,2013

3. Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells;Peters;Nature,2012

4. VariBench: a benchmark database for variations;Sasidharan Nair;Hum Mutat,2013

5. Interpretation, stratification and validation of sequence variants affecting mRNA splicing in complete human genome sequences;Shirley;Genomics Proteomics Bioinformatics,2013

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1. Choice of library size normalization and statistical methods for differential gene expression analysis in balanced two-group comparisons for RNA-seq studies;BMC Genomics;2020-01-28

2. S2k-Leitlinie Humangenetische Diagnostik und Genetische Beratung;Medizinische Genetik;2018-12-01

3. How does normalization impact RNA-seq disease diagnosis?;Journal of Biomedical Informatics;2018-09

4. Overcoming diagnostic issues in precision treatment of pancreatic cancer;Expert Review of Precision Medicine and Drug Development;2018-05-04

5. How Cytogenetics Paradigms Shape Decision Making in Translational Genomics;Human Genome Informatics;2018

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