Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline
Authors
Keywords
NGS data, Variant calling, Annotation, Clinical sequencing, Cloud computing
Journal
BMC BIOINFORMATICS
Volume 15, Issue 1, Pages 30
Publisher
Springer Nature
Online
2014-01-30
DOI
10.1186/1471-2105-15-30
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- ‘Big data’, Hadoop and cloud computing in genomics
- (2013) Aisling O’Driscoll et al. JOURNAL OF BIOMEDICAL INFORMATICS
- Whole-genome sequence–based analysis of high-density lipoprotein cholesterol
- (2013) Alanna C Morrison et al. NATURE GENETICS
- Chipster: user-friendly analysis software for microarray and other high-throughput data
- (2011) M Aleksi Kallio et al. BMC GENOMICS
- dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions
- (2011) Xiaoming Liu et al. HUMAN MUTATION
- Integrated genomic analyses of ovarian carcinoma
- (2011) D. Bell et al. NATURE
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- Exome Sequencing of Head and Neck Squamous Cell Carcinoma Reveals Inactivating Mutations in NOTCH1
- (2011) N. Agrawal et al. SCIENCE
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- Whole-Genome Sequencing in a Patient with Charcot–Marie–Tooth Neuropathy
- (2010) James R. Lupski et al. NEW ENGLAND JOURNAL OF MEDICINE
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Large-scale data integration framework provides a comprehensive view on glioblastoma multiforme
- (2010) Kristian Ovaska et al. Genome Medicine
- Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences
- (2010) Jeremy Goecks et al. GENOME BIOLOGY
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- A SNP discovery method to assess variant allele probability from next-generation resequencing data
- (2009) Y. Shen et al. GENOME RESEARCH
- Sequencing technologies — the next generation
- (2009) Michael L. Metzker NATURE REVIEWS GENETICS
- The complete genome of an individual by massively parallel DNA sequencing
- (2008) David A. Wheeler et al. NATURE
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now