Suppr超能文献

相似文献

1
eCOMPAGT -- efficient combination and management of phenotypes and genotypes for genetic epidemiology.
BMC Bioinformatics. 2009 May 11;10:139. doi: 10.1186/1471-2105-10-139.
3
Unleashing genotypes in epidemiology - A novel method for managing high throughput information.
J Biomed Inform. 2009 Dec;42(6):1029-34. doi: 10.1016/j.jbi.2009.07.005. Epub 2009 Jul 17.
4
An integrated system for genetic analysis.
BMC Bioinformatics. 2006 Apr 19;7:210. doi: 10.1186/1471-2105-7-210.
5
An integrated system for high throughput TaqMan based SNP genotyping.
Bioinformatics. 2001 Jul;17(7):654-5. doi: 10.1093/bioinformatics/17.7.654.
6
SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.
PLoS One. 2013;8(3):e59508. doi: 10.1371/journal.pone.0059508. Epub 2013 Mar 19.
7
GMFilter and SXTestPlate: software tools for improving the SNPlex genotyping system.
BMC Bioinformatics. 2009 Mar 9;10:81. doi: 10.1186/1471-2105-10-81.
9
RAMEDIS: the rare metabolic diseases database.
Appl Bioinformatics. 2006;5(2):115-8. doi: 10.2165/00822942-200605020-00006.
10
Gigwa v2-Extended and improved genotype investigator.
Gigascience. 2019 May 1;8(5). doi: 10.1093/gigascience/giz051.

本文引用的文献

1
Genome-wide association studies: a new window into immune-mediated diseases.
Nat Rev Immunol. 2008 Aug;8(8):631-43. doi: 10.1038/nri2361.
3
SNPLims: a data management system for genome wide association studies.
BMC Bioinformatics. 2008 Mar 26;9 Suppl 2(Suppl 2):S13. doi: 10.1186/1471-2105-9-S2-S13.
4
Genome-wide association studies in aging-related processes such as diabetes mellitus, atherosclerosis and cancer.
Exp Gerontol. 2008 Jan;43(1):39-43. doi: 10.1016/j.exger.2007.09.005. Epub 2007 Sep 29.
5
MLGA--a rapid and cost-efficient assay for gene copy-number analysis.
Nucleic Acids Res. 2007;35(17):e115. doi: 10.1093/nar/gkm651. Epub 2007 Sep 6.
6
Replicating genotype-phenotype associations.
Nature. 2007 Jun 7;447(7145):655-60. doi: 10.1038/447655a.
7
Global variation in copy number in the human genome.
Nature. 2006 Nov 23;444(7118):444-54. doi: 10.1038/nature05329.
8
Common genetic variants for breast cancer: 32 largely refuted candidates and larger prospects.
J Natl Cancer Inst. 2006 Oct 4;98(19):1350-3. doi: 10.1093/jnci/djj392.
9
An integrated system for genetic analysis.
BMC Bioinformatics. 2006 Apr 19;7:210. doi: 10.1186/1471-2105-7-210.
10
T.I.M.S: TaqMan Information Management System, tools to organize data flow in a genotyping laboratory.
BMC Bioinformatics. 2005 Oct 12;6:246. doi: 10.1186/1471-2105-6-246.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验