FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies-Reference-Cited by-同舟云学术

FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease Studies

Published:2016-06-06 Issue:6 Volume:12 Page:e1004980
ISSN:1553-7358
Container-title:PLOS Computational Biology
language:en
Short-container-title:PLoS Comput Biol

Author:

Chung Ren-Hua,Tsai Wei-Yun,Kang Chen-Yu,Yao Po-Ju,Tsai Hui-Ju,Chen Chia-Hsiang

Funder

Ministry of Science and Technology in Taiwan

National Health Research Institutes

Publisher

Public Library of Science (PLoS)

Subject

Computational Theory and Mathematics,Cellular and Molecular Neuroscience,Genetics,Molecular Biology,Ecology,Modelling and Simulation,Ecology, Evolution, Behavior and Systematics

Reference50 articles.

1. A survey of tools for variant analysis of next-generation genome sequencing data;S Pabinger;Brief Bioinform,2014

2. Integrated annotation and analysis of genetic variants from next-generation sequencing studies with variant tools;FA San Lucas;Bioinformatics,2012

3. VAAST 2.0: improved variant classification and disease-gene identification using a conservation-controlled amino acid substitution matrix;H Hu;Genet Epidemiol,2013

4. The role of large pedigrees in an era of high-throughput sequencing;EM Wijsman;Hum Genet,2012

5. VAR-MD: a tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance;M Sincan;Hum Mutat,2012

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3. PathOS: a decision support system for reporting high throughput sequencing of cancers in clinical diagnostic laboratories;Genome Medicine;2017-04-24

4. Pedigree based DNA sequencing pipeline for germline genomes of cancer families;Hereditary Cancer in Clinical Practice;2016-08-09