articles
- 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