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BMC Proceedings|December 13, 2019
Correction to: Community participation and private sector engagement are fundamental to achieving universal health coverage and health security in Africa: reflections from the second Africa health forumOlushayo Olu, Pamela Drameh-Avognon, Emil Asamoah-Odei, et al.BMC Proceedings|September 18, 2020
Growth faltering in early infancy: highlights from a two-day scientific consultationSatinder Aneja, Praveen Kumar, Tarun Shankar Choudhary, et al.BMC Proceedings|September 20, 2014
Understanding the sequence requirements of protein families: insights from the BioVis 2013 contestsWilliam C Ray, R Wolfgang Rumpf, Brandon Sullivan, et al.BMC Proceedings|September 20, 2014
Integrative visual analysis of protein sequence mutationsNadezhda T Doncheva, Karsten Klein, John H Morris, et al.BMC Proceedings|September 20, 2014
FixingTIM: interactive exploration of sequence and structural data to identify functional mutations in protein familiesTimothy Luciani, John Wenskovitch, Koonwah Chen, et al.BMC Proceedings|September 20, 2014
Mu-8: visualizing differences between proteins and their familiesJohnathan D Mercer, Balaji Pandian, Alexander Lex, et al.BMC Proceedings|September 20, 2014
Sequence Diversity Diagram for comparative analysis of multiple sequence alignmentsRyo Sakai, Jan AertsBMC Proceedings|March 1, 2012
Population structure analysis using rare and common functional variantsTesfaye M Baye, Hua He, Lili Ding, et al.BMC Proceedings|March 1, 2012
Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 dataJenna Sykes, Lu Cheng, Wei Xu, et al.BMC Proceedings|March 1, 2012
A novel method to detect rare variants using both family and unrelated case-control dataTao Feng, Robert C Elston, Xiaofeng ZhuPageof 102