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Genome Biology

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Overview

articles

  • A vast resource of allelic expression data spanning human tissues.  21. 2020
  • An amplicon-based sequencing framework for accurately measuring intrahost virus diversity using PrimalSeq and iVar.  20. 2019
  • The continuously evolving CRISPR barcoding toolbox.  19. 2018
  • A statistical framework for analyzing deep mutational scanning data.  18. 2017
  • GNB5 mutation causes a novel neuropsychiatric disorder featuring attention deficit hyperactivity disorder, severely impaired language development and normal cognition.  17. 2016
  • High-performance web services for querying gene and variant annotation.  17. 2016
  • Identifying candidate drivers of alcohol dependence-induced excessive drinking by assembly and interrogation of brain-specific regulatory networks.  16. 2015
  • Tools and best practices for data processing in allelic expression analysis.  16. 2015
  • Deep sequencing reveals cell-type-specific patterns of single-cell transcriptome variation.  16:122. 2015
  • An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.  15:R53. 2014
  • Enhanced methods for unbiased deep sequencing of Lassa and Ebola RNA viruses from clinical and biological samples.  15:519. 2014
  • Organizing knowledge to enable personalization of medicine in cancer.  15:438. 2014
  • A blood based 12-miRNA signature of Alzheimer disease patients.  14:R78. 2013
  • Pervasive and dynamic protein binding sites of the mRNA transcriptome in Saccharomyces cerevisiae.  14:R13. 2013
  • The transcription factor encyclopedia.  13:R24. 2012
  • Detection of low prevalence somatic mutations in solid tumors with ultra-deep targeted sequencing.  12. 2011
  • Games with a scientific purpose.  12:135. 2011
  • Population sequencing of two endocannabinoid metabolic genes identifies rare and common regulatory variants associated with extreme obesity and metabolite level.  11:R118. 2010
  • Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing.  11:R114. 2010
  • Towards a comprehensive structural variation map of an individual human genome.  11:R52. 2010
  • Induced pluripotent stem cells free of exogenous reprogramming factors.  10. 2009
  • Biogps: An extensible and customizable portal for querying and organizing gene annotation resources.  10:R130. 2009
  • Enrichment of sequencing targets from the human genome by solution hybridization.  10:R116. 2009
  • Evaluation of next generation sequencing platforms for population targeted sequencing studies.  10:R32. 2009
  • Exploring the transcriptional landscape of plant circadian rhythms using genome tiling arrays.  10:R17. 2009
  • Use of high-density tiling microarrays to identify mutations globally and elucidate mechanisms of drug resistance in plasmodium falciparum.  10:R21. 2009
  • Genetic determinants of phenotypic diversity in humans.  9:215. 2008
  • Global transcriptome analysis reveals circadian regulation of key pathways in plant growth and development.  9:R130. 2008
  • The proteome of Toxoplasma gondii: integration with the genome provides novel insights into gene expression and annotation.  9:R116. 2008
  • DNA variation and brain region-specific expression profiles exhibit different relationships between inbred mouse strains: Implications for eqtl mapping studies.  8:R25. 2007
  • Mobilization of pro-inflammatory lipids in obese plscr3-deficient mice.  8:R38. 2007
  • Power-law-like distributions in biomedical publications and research funding.  8:404. 2007
  • Circadian rhythms lit up in Chlamydomonas.  7:215. 2006
  • Genomic studies of mood disorders: the brain as a muscle?.  6. 2005
  • Microrna profiling of the murine hematopoietic system.  6:r71. 2005
  • Organellar proteomics: the prizes and pitfalls of opening the nuclear envelope.  3:1008.1. 2002
  • Chemical genomics: what will it take and who gets to play?.  2. 2001
  • Intraepithelial gamma delta T cells exposed by functional genomics.  2:1031. 2001
  • Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4).  1:research002-research002.10. 2000
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Identity

International Standard Serial Number (ISSN)

  • 1465-6906

Electronic International Standard Serial Number (EISSN)

  • 1465-6914

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