2012年8月17日星期五

Study designs column from Nature Reviews Genetics

http://www.nature.com/nrg/series/studydesigns/index.html


2012

September 2012 Volume 13 No 9

The continuing value of twin studies in the omics era

Jenny van Dongen, P. Eline Slagboom, Harmen H. M. Draisma, Nicholas G. Martin & Dorret I. Boomsma
doi:10.1038/nrg3243
August 2012 Volume 13 No 8

Studying and modelling dynamic biological processes using time-series gene expression data

Ziv Bar-Joseph, Anthony Gitter & Itamar Simon
doi:10.1038/nrg3244
May 2012 Volume 13 No 5

Molecular phylogenetics: principles and practice

Ziheng Yang & Bruce Rannala
doi:10.1038/nrg3186
May 2012 Volume 13 No 5

Harnessing genomics and genome biology to understand malaria biology

Sarah K. Volkman, Daniel E. Neafsey, Stephen F. Schaffner, Daniel J. Park & Dyann F. Wirth
doi:10.1038/nrg3187
May 2012 Volume 13 No 5

A beginner's guide to eukaryotic genome annotation

Mark Yandell and Daniel Ence
doi:10.1038/nrg3186
February 2012 Volume 13 No 2

Computer simulations: tools for population and evolutionary genetics

Sean Hoban, Giorgio Bertorelle & Oscar E. Gaggiotti
doi:10.1038/nrg3130
January 2012 Volume 13 No 1

Experimental and analytical tools for studying the human microbiome

Justin Kuczynski, Christian L. Lauber, William A. Walters, Laura Wegener Parfrey, José C. Clemente, Dirk Gevers & Rob Knight
doi:10.1038/nrg3129
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2011

December 2011 Volume 12 No 12

Software for systems biology: from tools to integrated platforms

Samik Ghosh, Yukiko Matsuoka, Yoshiyuki Asai, Kun-Yi Hsin & Hiroaki Kitano
doi:10.1038/nrg3096
November 2011 Volume 12 No 11

Molecular spandrels: tests of adaptation at the genetic level

Rowan D. H. Barrett & Hopi E. Hoekstra
doi:10.1038/nrg3015
November 2011 Volume 12 No 11

Exome sequencing as a tool for Mendelian disease gene discovery

Michael J. Bamshad, Sarah B. Ng, Abigail W. Bigham, Holly K. Tabor, Mary J. Emond,Deborah A. Nickerson & Jay Shendure
doi:10.1038/nrg3031
October 2011 Volume 12 No 10

Next-generation transcriptome assembly

Jeffrey A. Martin & Zhong Wang
doi:10.1038/nrg3068
October 2011 Volume 12 No 10

Haplotype phasing: existing methods and new developments

Sharon R. Browning & Brian L. Browning
doi:10.1038/nrg3054
August 2011 Volume 12 No 8

New approaches to disease mapping in admixed populations

Michael F. Seldin, Bogdan Pasaniuc & Alkes L. Price
doi:10.1038/nrg3002
August 2011 Volume 12 No 8

Epigenome-wide association studies for common human diseases

Vardhman K. Rakyan, Thomas A. Down, David J. Balding & Stephan Beck
doi:10.1038/nrg3000
July 2011 Volume 12 No 7

Genome-wide genetic marker discovery and genotyping using next-generation sequencing

John W. Davey, Paul A. Hohenlohe, Paul D. Etter, Jason Q. Boone, Julian M. Catchen & Mark L. Blaxter
doi:10.1038/nrg3012
June 2011 Volume 12 No 6

Genotype and SNP calling from next-generation sequencing data

Rasmus Nielsen, Joshua S. Paul, Anders Albrechtsen & Yun S. Song
doi:10.1038/nrg2986
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