Genome sequencing and comparison of two nonhuman primate animal models, the cynomolgus and Chinese rhesus macaques - Nature Biotechnology
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Genome sequence and analysis of the tuber crop potato - Nature
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Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia - Nature
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Volume 39 Issue suppl_2 | Nucleic Acids Research | Oxford Academic
Nucleic Acids Research, Volume 39, Issue suppl_2, 1 July 2011, Pages W1–W2, https://doi.org/10.1093/nar/gkr515
片頭痛に関連する遺伝的多型 （Nature Genetics）: NPG Nature Asia-Pacific
Nature姉妹誌 注目のハイライト 片頭痛に関連する遺伝的多型 Variants associated with migraine Nature Genetics, 2011年06月13日 普通型片頭痛に対する感受性に関連する遺伝的多型が同定された。この成果を報告する論文が、Nature Genetics（電子版）に掲載される。片頭痛は、高頻度に見られる異質性の高い神経疾患で、神経科外来患者の最大20％が罹患しており、男性より女性の患者数が多い。今回、M Schuerksらは、地域住民を対象とした研究における片頭痛を訴える5122人の女性と片頭痛を訴えていない1万8103人の女性を対象として、普通型片頭痛のゲノムワイド関連解析を行ったことを報告している。その結果、片頭痛に対する感受性に関連する3つのゲノム領域が同定され、そのうちの2つは、非片頭痛性頭痛と比べて、片頭痛に特異的だった。そ
Direct reprogramming of somatic cells is promoted by maternal transcription factor Glis1 - Nature
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Genetic origins of the Minoans and Mycenaeans
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Microarrays, deep sequencing and the true measure of the transcriptome - BMC Biology
Review Open access Published: 31 May 2011 Microarrays, deep sequencing and the true measure of the transcriptome John H Malone1 & Brian Oliver1 BMC Biology volume 9, Article number: 34 (2011) Cite this article Microarrays first made the analysis of the transcriptome possible, and have produced much important information. Today, however, researchers are increasingly turning to direct high-throughpu
RNA-seq: technical variability and sampling - BMC Genomics
Research article Open access Published: 06 June 2011 RNA-seq: technical variability and sampling Lauren M McIntyre1, Kenneth K Lopiano2, Alison M Morse1, Victor Amin1, Ann L Oberg3, Linda J Young2 & …Sergey V Nuzhdin4 Show authors BMC Genomics volume 12, Article number: 293 (2011) Cite this article BackgroundRNA-seq is revolutionizing the way we study transcriptomes. mRNA can be surveyed without p
Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing | Science Translational Medicine
Carrier Testing for Severe Childhood Recessive Diseases by Next-Generation Sequencing Callum J. Bell1,*, Darrell L. Dinwiddie1,2,*, Neil A. Miller1,2, Shannon L. Hateley1, Elena E. Ganusova1, Joann Mudge1, Ray J. Langley1, Lu Zhang3, Clarence C. Lee4, Faye D. Schilkey1, Vrunda Sheth4, Jimmy E. Woodward1, Heather E. Peckham4, Gary P. Schroth3, Ryan W. Kim1 and Stephen F. Kingsmore1,2,†1National Cen
Computational methods for transcriptome annotation and quantification using RNA-seq - Nature Methods
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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources - Nature Protocols
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RNA sequencing: advances, challenges and opportunities
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations - Nature Genetics
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One cell at a time - Nature Reviews Cancer