相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。RSEQtools: a modular framework to analyze RNA-Seq data using compact, anonymized data summaries
Lukas Habegger et al.
BIOINFORMATICS (2011)
The variant call format and VCFtools
Petr Danecek et al.
BIOINFORMATICS (2011)
Discovery of non-ETS gene fusions in human prostate cancer using next-generation RNA sequencing
Dorothee Pflueger et al.
GENOME RESEARCH (2011)
Efficient storage of high throughput DNA sequencing data using reference-based compression
Markus Hsi-Yang Fritz et al.
GENOME RESEARCH (2011)
Haplotype-resolved genome sequencing of a Gujarati Indian individual
Jacob O. Kitzman et al.
NATURE BIOTECHNOLOGY (2011)
Elucidating the inosinome: global approaches to adenosine-to-inosine RNA editing
Bjorn-Erik Wulff et al.
NATURE REVIEWS GENETICS (2011)
Transcriptome genetics using second generation sequencing in a Caucasian population
Stephen B. Montgomery et al.
NATURE (2010)
Understanding mechanisms underlying human gene expression variation with RNA sequencing
Joseph K. Pickrell et al.
NATURE (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
Cloud computing and the DNA data race
Michael C. Schatz et al.
NATURE BIOTECHNOLOGY (2010)
APPLICATIONS OF NEXT-GENERATION SEQUENCING Sequencing technologies - the next generation
Michael L. Metzker
NATURE REVIEWS GENETICS (2010)
A Draft Sequence of the Neandertal Genome
Richard E. Green et al.
SCIENCE (2010)
The $1,000 genome, the $100,000 analysis?
Elaine R. Mardis
GENOME MEDICINE (2010)
The case for cloud computing in genome informatics
Lincoln D. Stein
GENOME BIOLOGY (2010)
Cloud-scale RNA-sequencing differential expression analysis with Myrna
Ben Langmead et al.
GENOME BIOLOGY (2010)
Galaxy: a comprehensive approach for supporting accessible, reproducible, and transparent computational research in the life sciences
Jeremy Goecks et al.
GENOME BIOLOGY (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Chimeric transcript discovery by paired-end transcriptome sequencing
Christopher A. Maher et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Erez Lieberman-Aiden et al.
SCIENCE (2009)
Searching for SNPs with cloud computing
Ben Langmead et al.
GENOME BIOLOGY (2009)
Alternative isoform regulation in human tissue transcriptomes
Eric T. Wang et al.
NATURE (2008)
The complete genome of an individual by massively parallel DNA sequencing
David A. Wheeler et al.
NATURE (2008)
HITS-CLIP yields genome-wide insights into brain alternative RNA processing
Donny D. Licatalosi et al.
NATURE (2008)
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
Shawn J. Cokus et al.
NATURE (2008)
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis
Thomas A. Down et al.
NATURE BIOTECHNOLOGY (2008)
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Ali Mortazavi et al.
NATURE METHODS (2008)
Nascent RNA Sequencing Reveals Widespread Pausing and Divergent Initiation at Human Promoters
Leighton J. Core et al.
SCIENCE (2008)
A global view of gene activity and alternative splicing by deep sequencing of the human transcriptome
Marc Sultan et al.
SCIENCE (2008)
The impact of next-generation sequencing technology on genetics
Elaine R. Mardis
TRENDS IN GENETICS (2008)
Toward the $1000 human genome
ST Bennett et al.
PHARMACOGENOMICS (2005)
分享论文
