Ferret: a user-friendly Java tool to extract data from the 1000 Genomes Project
暂无分享,去创建一个
Sophie Limou | Andrew M. Taverner | Cheryl A. Winkler | Andrew M. Taverner | Sophie Limou | C. Winkler
[1] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[2] Kenny Q. Ye,et al. An integrated map of genetic variation from 1,092 human genomes , 2012, Nature.
[3] Manuel A. R. Ferreira,et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. , 2007, American journal of human genetics.
[4] Gregory D. Schuler,et al. Database resources of the National Center for Biotechnology Information: update , 2004, Nucleic acids research.
[5] Heng Li,et al. Tabix: fast retrieval of sequence features from generic TAB-delimited files , 2011, Bioinform..
[6] Elizabeth M. Smigielski,et al. dbSNP: the NCBI database of genetic variation , 2001, Nucleic Acids Res..
[7] T. Tatusova,et al. Entrez Gene: gene-centered information at NCBI , 2010, Nucleic Acids Res..
[8] Gonçalo R. Abecasis,et al. The variant call format and VCFtools , 2011, Bioinform..
[9] Emily H Turner,et al. Actionable, pathogenic incidental findings in 1,000 participants' exomes. , 2013, American journal of human genetics.
[10] Mark Daly,et al. Haploview: analysis and visualization of LD and haplotype maps , 2005, Bioinform..